"MAP4-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3041281	NM_001385682.1(MAP4):c.*138A>G	MAP4 (H1094R +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	MAP4-related condition	GBenign
Select item 3043744	NM_001385682.1(MAP4):c.*44G>A	MAP4 (D1063N +2 more)	Single nucleotide variant (missense variant +1 more)	MAP4-related condition	GLikely benign
Select item 3053586	NM_001385682.1(MAP4):c.6792C>T (p.Pro2264=)	MAP4	Single nucleotide variant (synonymous variant +1 more)	MAP4-related condition	GLikely benign
Select item 3039620	NM_001385682.1(MAP4):c.6726G>A (p.Leu2242=)	MAP4	Single nucleotide variant (synonymous variant +1 more)	MAP4-related condition	GLikely benign
Select item 3039009	NM_001385682.1(MAP4):c.6422C>T (p.Ser2141Phe)	MAP4 (S1008F +49 more)	Single nucleotide variant (missense variant +1 more)	MAP4-related condition	GLikely benign
Select item 3032804	NM_001385682.1(MAP4):c.6402G>A (p.Ala2134=)	MAP4	Single nucleotide variant (synonymous variant +1 more)	MAP4-related condition	GLikely benign
Select item 3057412	NM_001385682.1(MAP4):c.6384T>C (p.Ser2128=)	MAP4	Single nucleotide variant (synonymous variant +1 more)	MAP4-related condition	GLikely benign
Select item 3043041	NM_001385682.1(MAP4):c.6369C>T (p.Ala2123=)	MAP4	Single nucleotide variant (intron variant +1 more)	MAP4-related condition	GLikely benign
Select item 781710	NM_001385682.1(MAP4):c.5850G>A (p.Gln1950=)	MAP4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3040424	NM_001385682.1(MAP4):c.5760C>T (p.Pro1920=)	MAP4	Single nucleotide variant (synonymous variant)	MAP4-related condition	GLikely benign
Select item 3039645	NM_001385682.1(MAP4):c.5466G>C (p.Val1822=)	MAP4	Single nucleotide variant (synonymous variant)	MAP4-related condition	GBenign
Select item 3040872	NM_001385682.1(MAP4):c.1884C>G (p.Val628=)	MAP4 (I587M +1 more)	Single nucleotide variant (synonymous variant +2 more)	MAP4-related condition	GLikely benign
Select item 3060070	NM_001385682.1(MAP4):c.1882G>A (p.Val628Ile)	MAP4 (V179I +19 more)	Single nucleotide variant (missense variant +2 more)	MAP4-related condition	GBenign
Select item 3034981	NM_001385682.1(MAP4):c.1837G>A (p.Val613Met)	MAP4 (V402M +17 more)	Single nucleotide variant (missense variant +1 more)	MAP4-related condition	GLikely benign
Select item 3033770	NM_001385682.1(MAP4):c.1707T>C (p.Asn569=)	MAP4	Single nucleotide variant (synonymous variant +1 more)	MAP4-related condition	GLikely benign
Select item 3035749	NM_001385682.1(MAP4):c.1647C>T (p.Val549=)	MAP4	Single nucleotide variant (synonymous variant +1 more)	MAP4-related condition	GLikely benign
Select item 714945	NM_001385682.1(MAP4):c.1548G>A (p.Leu516=)	MAP4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3055750	NM_001385682.1(MAP4):c.1321G>C (p.Glu441Gln)	MAP4 (E230Q +17 more)	Single nucleotide variant (missense variant +1 more)	MAP4-related condition	GBenign
Select item 3048980	NM_001385682.1(MAP4):c.1311T>C (p.Ala437=)	MAP4	Single nucleotide variant (synonymous variant +1 more)	MAP4-related condition	GLikely benign
Select item 3059551	NM_001385682.1(MAP4):c.1280C>A (p.Ser427Tyr)	MAP4 (S279Y +16 more)	Single nucleotide variant (missense variant +1 more)	MAP4-related condition	GBenign
Select item 3035104	NM_001385682.1(MAP4):c.1156A>G (p.Ile386Val)	MAP4 (I238V +16 more)	Single nucleotide variant (missense variant +1 more)	MAP4-related condition	GBenign
Select item 3044324	NM_001385682.1(MAP4):c.647C>T (p.Thr216Met)	MAP4 (T109M +10 more)	Single nucleotide variant (missense variant +1 more)	MAP4-related condition	GBenign
Select item 3043861	NM_001385682.1(MAP4):c.403C>T (p.Pro135Ser)	MAP4 (P112S +6 more)	Single nucleotide variant (missense variant +1 more)	MAP4-related condition	GBenign
Select item 3055841	NM_001385682.1(MAP4):c.399C>T (p.Val133=)	MAP4	Single nucleotide variant (synonymous variant +1 more)	MAP4-related condition	GBenign
Select item 3047450	NM_001385682.1(MAP4):c.300A>G (p.Pro100=)	MAP4	Single nucleotide variant (synonymous variant +2 more)	MAP4-related condition	GLikely benign
Select item 3041545	NM_001385682.1(MAP4):c.292+2409G>A	MAP4	Single nucleotide variant (3 prime UTR variant +1 more)	MAP4-related condition	GLikely benign
Select item 790262	NM_001385682.1(MAP4):c.292+9T>G	MAP4	Single nucleotide variant (intron variant)	MAP4-related condition +1 more	GBenign/Likely benign
Select item 778072	NM_001385682.1(MAP4):c.111T>C (p.Val37=)	MAP4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 3056736	NM_001385682.1(MAP4):c.68G>A (p.Arg23Gln)	MAP4 (R23Q)	Single nucleotide variant (missense variant +1 more)	MAP4-related condition	GBenign
Select item 3034536	NM_001385682.1(MAP4):c.67C>T (p.Arg23Trp)	MAP4 (R23W)	Single nucleotide variant (missense variant +1 more)	MAP4-related condition	GLikely benign
Select item 3035813	NM_001385682.1(MAP4):c.60G>A (p.Glu20=)	MAP4	Single nucleotide variant (synonymous variant +1 more)	MAP4-related condition	GLikely benign
Select item 3043664	NM_001385682.1(MAP4):c.48C>T (p.Asp16=)	MAP4	Single nucleotide variant (synonymous variant +1 more)	MAP4-related condition	GLikely benign

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Items: 32