BRINP3[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 53

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2260515	NM_199051.3(BRINP3):c.2261C>A (p.Pro754Gln)	BRINP3 (P754Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135070	NM_199051.3(BRINP3):c.2138T>G (p.Leu713Arg)	BRINP3 (L611R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261774	NM_199051.3(BRINP3):c.2064C>G (p.Asp688Glu)	BRINP3 (D688E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135069	NM_199051.3(BRINP3):c.2038A>G (p.Ile680Val)	BRINP3 (I680V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306842	NM_199051.3(BRINP3):c.2029C>T (p.Pro677Ser)	BRINP3 (P575S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261772	NM_199051.3(BRINP3):c.2026G>T (p.Asp676Tyr)	BRINP3 (D574Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355944	NM_199051.3(BRINP3):c.1991A>G (p.Asn664Ser)	BRINP3 (N562S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400347	NM_199051.3(BRINP3):c.1907A>G (p.Asn636Ser)	BRINP3 (N636S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2281497	NM_199051.3(BRINP3):c.1898T>A (p.Ile633Asn)	BRINP3 (I633N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469638	NM_199051.3(BRINP3):c.1814T>C (p.Leu605Pro)	BRINP3 (L503P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605243	NM_199051.3(BRINP3):c.1630T>G (p.Ser544Ala)	BRINP3 (S544A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261771	NM_199051.3(BRINP3):c.1426C>T (p.Pro476Ser)	BRINP3 (P374S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135067	NM_199051.3(BRINP3):c.1415G>A (p.Gly472Glu)	BRINP3 (G370E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261775	NM_199051.3(BRINP3):c.1391A>T (p.Asn464Ile)	BRINP3 (N362I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541469	NM_199051.3(BRINP3):c.1390A>C (p.Asn464His)	BRINP3 (N362H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276342	NM_199051.3(BRINP3):c.1285C>G (p.Pro429Ala)	BRINP3 (P429A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478519	NM_199051.3(BRINP3):c.1270C>A (p.His424Asn)	BRINP3 (H424N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548316	NM_199051.3(BRINP3):c.1185A>C (p.Arg395Ser)	BRINP3 (R395S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524350	NM_199051.3(BRINP3):c.1175C>A (p.Pro392Gln)	BRINP3 (P290Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603578	NM_199051.3(BRINP3):c.1162C>A (p.Leu388Ile)	BRINP3 (L388I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135066	NM_199051.3(BRINP3):c.1130T>A (p.Phe377Tyr)	BRINP3 (F377Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135065	NM_199051.3(BRINP3):c.1082G>A (p.Ser361Asn)	BRINP3 (S259N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464502	NM_199051.3(BRINP3):c.1080C>G (p.Asn360Lys)	BRINP3 (N360K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390444	NM_199051.3(BRINP3):c.1061G>A (p.Arg354His)	BRINP3 (R354H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512919	NM_199051.3(BRINP3):c.1015T>A (p.Ser339Thr)	BRINP3 (S339T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135078	NM_199051.3(BRINP3):c.984A>T (p.Lys328Asn)	BRINP3 (K328N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489191	NM_199051.3(BRINP3):c.962A>G (p.Asp321Gly)	BRINP3 (D219G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555324	NM_199051.3(BRINP3):c.914G>A (p.Arg305Gln)	BRINP3 (R203Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135075	NM_199051.3(BRINP3):c.886A>G (p.Ile296Val)	BRINP3 (I296V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596354	NM_199051.3(BRINP3):c.826A>G (p.Asn276Asp)	BRINP3 (N276D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135074	NM_199051.3(BRINP3):c.661G>A (p.Asp221Asn)	BRINP3 (D119N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619117	NM_199051.3(BRINP3):c.521T>A (p.Leu174Gln)	BRINP3 (L174Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457778	NM_199051.3(BRINP3):c.512C>G (p.Ser171Trp)	BRINP3 (S171W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248115	NM_199051.3(BRINP3):c.347G>A (p.Arg116His)	BRINP3 (R116H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2230888	NM_199051.3(BRINP3):c.337C>G (p.Leu113Val)	BRINP3 (L113V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493900	NM_199051.3(BRINP3):c.335G>T (p.Arg112Ile)	BRINP3 (R112I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369929	NM_199051.3(BRINP3):c.331A>G (p.Ile111Val)	BRINP3 (I111V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3135073	NM_199051.3(BRINP3):c.262A>G (p.Asn88Asp)	BRINP3 (N88D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3135072	NM_199051.3(BRINP3):c.233A>G (p.Tyr78Cys)	BRINP3 (T40A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135071	NM_199051.3(BRINP3):c.217A>G (p.Thr73Ala)	BRINP3 (T73A)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2392681	NM_199051.3(BRINP3):c.203G>T (p.Arg68Leu)	BRINP3 (G30C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3135068	NM_199051.3(BRINP3):c.193G>A (p.Asp65Asn)	BRINP3 (W26* +1 more)	Single nucleotide variant (nonsense +1 more)	not specified	GUncertain significance
Select item 3135077	NM_199051.3(BRINP3):c.97G>C (p.Ala33Pro)	BRINP3 (A33P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3261773	NM_199051.3(BRINP3):c.13A>T (p.Ser5Cys)	BRINP3 (S5C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 979927	GRCh37/hg19 1q31.1-31.2(chr1:190098893-192114806)x1	BRINP3	Copy number loss	not provided	GUncertain significance
Select item 979317	GRCh37/hg19 1q31.1-31.2(chr1:189776412-191289591)x3	BRINP3	Copy number gain	not provided	GUncertain significance
Select item 979316	GRCh37/hg19 1q31.1(chr1:190226030-190304397)x1	BRINP3	Copy number loss	not provided	GUncertain significance
Select item 979315	GRCh37/hg19 1q31.1(chr1:190184943-190361454)x1	BRINP3	Copy number loss	not provided	GUncertain significance
Select item 814152	GRCh37/hg19 1q31.1(chr1:190186386-190675536)x3	BRINP3	Copy number gain	not provided	GUncertain significance
Select item 814151	GRCh37/hg19 1q31.1(chr1:190161138-190304397)x1	BRINP3	Copy number loss	not provided	GUncertain significance
Select item 688229	GRCh37/hg19 1q31.1(chr1:190177709-190356910)x1	BRINP3	Copy number loss	not provided	GUncertain significance
Select item 684545	Single allele	BRINP3	Deletion	not provided	Gnot provided
Select item 565206	GRCh37/hg19 1q31.1(chr1:189547624-190142512)x3	BRINP3	Copy number gain	not provided	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 53