MPDU1[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154089	GRCh38/hg38 17p13.3-12(chr17:150732-14764202)x3	ABR, ABR-AS1 +962 more	Copy number gain	See cases	GPathogenic
Select item 149531	GRCh38/hg38 17p13.3-12(chr17:162016-12343901)x3	LOC130059883, LOC130059884 +922 more	Copy number gain	See cases	GPathogenic
Select item 149158	GRCh38/hg38 17p13.3-13.1(chr17:162016-7697012)x1	TRARG1, TRPV1 +651 more	Copy number loss	See cases	GPathogenic
Select item 2579287	GRCh38/hg38 17p13.3-12(chr17:165730-11404096)x3	SAT2, SCARF1 +911 more	Copy number gain	Chromosome 17p13.3 duplication syndrome	GPathogenic
Select item 145484	GRCh38/hg38 17p13.2-12(chr17:5732953-12095349)x3	ACADVL, ACAP1 +461 more	Copy number gain	See cases	GPathogenic
Select item 57356	GRCh38/hg38 17p13.2-13.1(chr17:5732977-8038822)x1	SPEM3, TEKT1 +229 more	Copy number loss	See cases	GPathogenic
Select item 149166	GRCh38/hg38 17p13.2-13.1(chr17:6361393-7750863)x3	ACADVL, ACAP1 +182 more	Copy number gain	See cases	GLikely pathogenic
Select item 59583	GRCh38/hg38 17p13.1(chr17:7478195-8435524)x1	ALOX12B, ALOX15B +191 more	Copy number loss	See cases	GPathogenic
Select item 150702	GRCh38/hg38 17p13.1(chr17:7544902-7670581)x3	ATP1B2, CD68 +36 more	Copy number gain	See cases	GUncertain significance
Select item 325508	NM_004870.3(MPDU1):c.-182G>C	MPDU1, MPDU1-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	Congenital disorder of glycosylation	GUncertain significance
Select item 325509	NM_004870.3(MPDU1):c.-139G>A	MPDU1, MPDU1-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	Congenital disorder of glycosylation	GUncertain significance
Select item 325510	NM_004870.3(MPDU1):c.-108G>A	MPDU1, MPDU1-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	Congenital disorder of glycosylation	GUncertain significance
Select item 325511	NM_004870.3(MPDU1):c.-73A>G	MPDU1, MPDU1-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	Congenital disorder of glycosylation +1 more	GBenign/Likely benign
Select item 325512	NM_004870.3(MPDU1):c.-36C>T	MPDU1, MPDU1-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 382610	NM_004870.3(MPDU1):c.-34G>A	MPDU1, MPDU1-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 5869	NM_004870.4(MPDU1):c.2T>C (p.Met1Thr)	MPDU1, MPDU1-AS1 (M1T)	Single nucleotide variant (missense variant +2 more)	MPDU1-congenital disorder of glycosylation	GPathogenic
Select item 570180	NM_004870.4(MPDU1):c.10G>A (p.Glu4Lys)	MPDU1, MPDU1-AS1 (E4K)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 389197	NM_004870.4(MPDU1):c.12G>A (p.Glu4=)	MPDU1, MPDU1-AS1	Single nucleotide variant (synonymous variant +1 more)	MPDU1-congenital disorder of glycosylation +1 more	GLikely benign
Select item 684508	NM_004870.4(MPDU1):c.19G>T (p.Gly7Ter)	MPDU1, MPDU1-AS1 (G7*)	Single nucleotide variant (nonsense +1 more)	Inborn genetic diseases	GLikely pathogenic
Select item 2240105	NM_004870.4(MPDU1):c.23C>T (p.Pro8Leu)	MPDU1, MPDU1-AS1 (P8L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 703002	NM_004870.4(MPDU1):c.24G>C (p.Pro8=)	MPDU1, MPDU1-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3352747	NM_004870.4(MPDU1):c.36G>A (p.Leu12=)	MPDU1, MPDU1-AS1	Single nucleotide variant (synonymous variant +1 more)	MPDU1-related disorder	GLikely benign
Select item 325513	NM_004870.4(MPDU1):c.43C>T (p.Pro15Ser)	MPDU1, MPDU1-AS1 (P15S)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 889661	NM_004870.4(MPDU1):c.53T>C (p.Leu18Ser)	MPDU1-AS1, MPDU1 (L18S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 3201147	NM_004870.4(MPDU1):c.56C>T (p.Pro19Leu)	MPDU1, MPDU1-AS1 (P19L)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1034127	NM_004870.4(MPDU1):c.66C>G (p.Cys22Trp)	LOC100996842, MPDU1 (C22W)	Single nucleotide variant (non-coding transcript variant +1 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 1333683	NM_004870.4(MPDU1):c.69del (p.Cys22_Tyr23insTer)	MPDU1, MPDU1-AS1	Deletion (non-coding transcript variant +1 more)	MPDU1-congenital disorder of glycosylation	GLikely pathogenic
Select item 889662	NM_004870.4(MPDU1):c.84T>C (p.Val28=)	MPDU1, MPDU1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 2465500	NM_004870.4(MPDU1):c.91G>C (p.Asp31His)	MPDU1, MPDU1-AS1 (D31H)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1582606	NM_004870.4(MPDU1):c.103+19C>T	MPDU1, MPDU1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	MPDU1-congenital disorder of glycosylation	GLikely benign
Select item 1325936	NM_004870.4(MPDU1):c.103+102T>C	MPDU1, MPDU1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1228784	NM_004870.4(MPDU1):c.104-195_104-194del	MPDU1	Deletion (intron variant)	not provided	GBenign
Select item 386602	NM_004870.4(MPDU1):c.114C>G (p.Leu38=)	MPDU1	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 325514	NM_004870.4(MPDU1):c.121C>G (p.Leu41Val)	MPDU1 (L41V)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation	GConflicting classifications of pathogenicity
Select item 2324544	NM_004870.4(MPDU1):c.127A>C (p.Ser43Arg)	MPDU1 (S43R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2492692	NM_004870.4(MPDU1):c.134G>T (p.Gly45Val)	MPDU1 (G45V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 996029	NM_004870.4(MPDU1):c.137T>C (p.Leu46Pro)	MPDU1 (L46P)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 1302252	NM_004870.4(MPDU1):c.149T>C (p.Ile50Thr)	MPDU1 (I50T)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation +1 more	GUncertain significance
Select item 2237774	NM_004870.4(MPDU1):c.169+4T>G	MPDU1	Single nucleotide variant (intron variant)	Inborn genetic diseases	GUncertain significance
Select item 1970053	NM_004870.4(MPDU1):c.170-1G>A	MPDU1	Single nucleotide variant (splice acceptor variant)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 1017785	NM_004870.4(MPDU1):c.184G>A (p.Val62Met)	MPDU1 (V62M)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 889663	NM_004870.4(MPDU1):c.189T>G (p.Phe63Leu)	MPDU1 (F63L)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 761854	NM_004870.4(MPDU1):c.207G>A (p.Lys69=)	MPDU1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 5867	NM_004870.4(MPDU1):c.218G>A (p.Gly73Glu)	MPDU1 (G73E)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation +1 more	GConflicting classifications of pathogenicity
Select item 5871	NM_004870.4(MPDU1):c.221T>C (p.Leu74Ser)	MPDU1 (L74S)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation	GPathogenic
Select item 2485699	NM_004870.4(MPDU1):c.230A>C (p.Gln77Pro)	MPDU1 (Q77P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 259558	NM_004870.4(MPDU1):c.302+21C>T	MPDU1	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 1283837	NM_004870.4(MPDU1):c.303-240_303-239del	MPDU1	Deletion (intron variant)	not provided	GBenign
Select item 1347327	NM_004870.4(MPDU1):c.303-16A>G	MPDU1	Single nucleotide variant (intron variant)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 1651094	NM_004870.4(MPDU1):c.303-9A>G	MPDU1	Single nucleotide variant (intron variant)	MPDU1-congenital disorder of glycosylation	GLikely benign
Select item 495318	NM_004870.4(MPDU1):c.310G>A (p.Gly104Ser)	MPDU1 (G104S)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation	GLikely pathogenic
Select item 1903250	NM_004870.4(MPDU1):c.337A>T (p.Thr113Ser)	MPDU1 (T113S)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 889664	NM_004870.4(MPDU1):c.338C>T (p.Thr113Met)	MPDU1 (T113M)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation +1 more	GUncertain significance
Select item 5868	NM_004870.4(MPDU1):c.356T>C (p.Leu119Pro)	MPDU1 (L119P)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation	GPathogenic
Select item 495319	NM_004870.4(MPDU1):c.377A>C (p.Gln126Pro)	MPDU1 (Q126P)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation	GLikely pathogenic
Select item 740426	NM_004870.4(MPDU1):c.388+10A>G	MPDU1 (D133G)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3064734	NM_004870.4(MPDU1):c.388+17del	MPDU1 (K136fs)	Deletion (frameshift variant +1 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 681461	NM_004870.4(MPDU1):c.388+16C>G	MPDU1 (P135R)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2647366	NM_004870.4(MPDU1):c.388+59C>G	MPDU1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 325515	NM_004870.4(MPDU1):c.393C>T (p.Val131=)	MPDU1	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3201135	NM_004870.4(MPDU1):c.400C>G (p.Leu134Val)	MPDU1 (L134V)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 851551	NM_004870.4(MPDU1):c.403G>A (p.Ala135Thr)	MPDU1 (A135T)	Single nucleotide variant (missense variant +2 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 95180	NM_004870.4(MPDU1):c.403G>C (p.Ala135Pro)	MPDU1 (A135P)	Single nucleotide variant (missense variant +2 more)	MPDU1-congenital disorder of glycosylation +2 more	GBenign
Select item 1937258	NM_004870.4(MPDU1):c.410A>G (p.Tyr137Cys)	MPDU1 (Y137C)	Single nucleotide variant (missense variant +2 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 325516	NM_004870.4(MPDU1):c.411C>T (p.Tyr137=)	MPDU1	Single nucleotide variant (synonymous variant +2 more)	MPDU1-congenital disorder of glycosylation +1 more	GConflicting classifications of pathogenicity
Select item 891228	NM_004870.4(MPDU1):c.437C>T (p.Ser146Leu)	MPDU1 (S146L)	Single nucleotide variant (missense variant +2 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 736476	NM_004870.4(MPDU1):c.444G>A (p.Leu148=)	MPDU1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 325517	NM_004870.4(MPDU1):c.450C>T (p.Pro150=)	MPDU1	Single nucleotide variant (synonymous variant +2 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 3252901	NM_004870.4(MPDU1):c.452del (p.Pro150_Leu151insTer)	MPDU1	Deletion (nonsense +2 more)	not provided	GUncertain significance
Select item 1956438	NM_004870.4(MPDU1):c.468G>A (p.Leu156=)	MPDU1	Single nucleotide variant (synonymous variant +2 more)	MPDU1-congenital disorder of glycosylation	GLikely benign
Select item 533016	NM_004870.4(MPDU1):c.477del (p.Ser160fs)	MPDU1 (S160fs)	Deletion (frameshift variant +2 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 3201138	NM_004870.4(MPDU1):c.482A>G (p.Asn161Ser)	MPDU1 (N161S)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 259559	NM_004870.4(MPDU1):c.507+44G>C	MPDU1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 325518	NM_004870.4(MPDU1):c.508-9C>T	MPDU1	Single nucleotide variant (intron variant)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 523948	NM_004870.4(MPDU1):c.511del (p.Leu171fs)	MPDU1 (S152fs +1 more)	Deletion (frameshift variant +1 more)	MPDU1-congenital disorder of glycosylation +2 more	GConflicting classifications of pathogenicity
Select item 930801	NM_004870.4(MPDU1):c.514C>T (p.Gln172Ter)	MPDU1 (Q172*)	Single nucleotide variant (synonymous variant +2 more)	MPDU1-congenital disorder of glycosylation	GLikely pathogenic
Select item 774455	NM_004870.4(MPDU1):c.537C>T (p.Asn179=)	MPDU1 (T160M)	Single nucleotide variant (missense variant +2 more)	MPDU1-congenital disorder of glycosylation	GLikely benign
Select item 325519	NM_004870.4(MPDU1):c.560C>T (p.Ala187Val)	MPDU1 (A187V +1 more)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation +2 more	GUncertain significance
Select item 817696	NM_004870.4(MPDU1):c.566_567del (p.Thr189fs)	MPDU1 (T189fs +1 more)	Microsatellite (frameshift variant +1 more)	not provided	GLikely pathogenic
Select item 1036624	NM_004870.4(MPDU1):c.573C>A (p.Phe191Leu)	MPDU1 (S172Y +1 more)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 1137819	NM_004870.4(MPDU1):c.582T>C (p.Phe194=)	MPDU1 (L175S)	Single nucleotide variant (missense variant +2 more)	MPDU1-congenital disorder of glycosylation	GLikely benign
Select item 2052017	NM_004870.4(MPDU1):c.589T>C (p.Ser197Pro)	MPDU1 (S197P)	Single nucleotide variant (synonymous variant +2 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 1661950	NM_004870.4(MPDU1):c.591C>G (p.Ser197=)	MPDU1 (P178R)	Single nucleotide variant (missense variant +2 more)	MPDU1-congenital disorder of glycosylation	GLikely benign
Select item 966796	NM_004870.4(MPDU1):c.599G>A (p.Arg200Gln)	MPDU1 (R200Q +1 more)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 1034126	NM_004870.4(MPDU1):c.613A>G (p.Ile205Val)	MPDU1 (I205V)	Single nucleotide variant (synonymous variant +2 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 387361	NM_004870.4(MPDU1):c.618+14C>T	MPDU1	Single nucleotide variant (intron variant)	MPDU1-congenital disorder of glycosylation +1 more	GConflicting classifications of pathogenicity
Select item 2691673	NM_004870.4(MPDU1):c.619-17C>G	MPDU1	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 631790	NM_004870.4(MPDU1):c.619-2A>G	MPDU1	Single nucleotide variant (splice acceptor variant)	MPDU1-congenital disorder of glycosylation +1 more	GConflicting classifications of pathogenicity
Select item 1511958	NM_004870.4(MPDU1):c.631C>G (p.Pro211Ala)	MPDU1 (I191M +1 more)	Single nucleotide variant (missense variant +1 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance
Select item 1628852	NM_004870.4(MPDU1):c.636G>C (p.Leu212=)	MPDU1	Single nucleotide variant (stop lost +2 more)	MPDU1-congenital disorder of glycosylation	GLikely benign
Select item 2515648	NM_004870.4(MPDU1):c.644G>A (p.Gly215Glu)	MPDU1 (G215E)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 509198	NM_004870.4(MPDU1):c.648C>T (p.Thr216=)	MPDU1	Single nucleotide variant (3 prime UTR variant +2 more)	MPDU1-congenital disorder of glycosylation +1 more	GLikely benign
Select item 703364	NM_004870.4(MPDU1):c.652G>T (p.Val218Leu)	MPDU1 (V218L)	Single nucleotide variant (3 prime UTR variant +2 more)	MPDU1-congenital disorder of glycosylation	GBenign/Likely benign
Select item 2663022	NM_004870.4(MPDU1):c.666_667del (p.Cys223fs)	MPDU1 (C223fs)	Microsatellite (3 prime UTR variant +2 more)	not provided	GLikely pathogenic
Select item 703346	NM_004870.4(MPDU1):c.662C>G (p.Ser221Cys)	MPDU1 (S221C)	Single nucleotide variant (3 prime UTR variant +2 more)	MPDU1-congenital disorder of glycosylation	GLikely benign
Select item 682554	NM_004870.4(MPDU1):c.672C>T (p.Asn224=)	MPDU1	Single nucleotide variant (3 prime UTR variant +2 more)	not provided +1 more	GLikely benign
Select item 325520	NM_004870.4(MPDU1):c.673G>A (p.Gly225Ser)	MPDU1 (G225S)	Single nucleotide variant (3 prime UTR variant +2 more)	not provided +2 more	GBenign
Select item 95181	NM_004870.4(MPDU1):c.685G>A (p.Ala229Thr)	MPDU1 (A229T)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified +2 more	GBenign
Select item 3201154	NM_004870.4(MPDU1):c.703T>C (p.Trp235Arg)	MPDU1 (W235R)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 1444219	NM_004870.4(MPDU1):c.713A>G (p.Lys238Arg)	MPDU1 (K238R)	Single nucleotide variant (3 prime UTR variant +2 more)	MPDU1-congenital disorder of glycosylation	GUncertain significance

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