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

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2248391	NM_001196.4(BID):c.547C>T (p.Arg183Cys)	BID (R183C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385140	NM_001196.4(BID):c.500T>C (p.Leu167Pro)	BID (L213P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260930	NM_001196.4(BID):c.491C>T (p.Pro164Leu)	BID (P68L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385882	NM_001196.4(BID):c.488C>T (p.Thr163Met)	BID (T209M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3133992	NM_001196.4(BID):c.444G>A (p.Met148Ile)	BID (M148I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489568	NM_001196.4(BID):c.385A>G (p.Thr129Ala)	BID (T129A +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3260928	NM_001196.4(BID):c.374G>A (p.Arg125Lys)	BID (R29K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3133990	NM_001196.4(BID):c.368G>A (p.Arg123Gln)	BID (R123Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486823	NM_001196.4(BID):c.317T>G (p.Val106Gly)	BID (V10G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260929	NM_001196.4(BID):c.311G>T (p.Gly104Val)	BID (G104V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591609	NM_001196.4(BID):c.308C>T (p.Pro103Leu)	BID (P149L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244851	NM_001196.4(BID):c.305C>T (p.Pro102Leu)	BID (P102L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521429	NM_001196.4(BID):c.263G>A (p.Arg88Lys)	BID (R134K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214941	NM_001196.4(BID):c.250C>T (p.Arg84Trp)	BID (R130W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3133989	NM_001196.4(BID):c.227C>G (p.Ser76Cys)	BID (S76C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3133988	NM_001196.4(BID):c.188G>C (p.Arg63Pro)	BID (R63P +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2289577	NM_001196.4(BID):c.178G>A (p.Asp60Asn)	BID (D106N +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2394869	NM_001196.4(BID):c.100C>T (p.Arg34Cys)	BID (R80C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3260931	NM_001196.4(BID):c.-15C>T	BID (R42C)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2358567	NM_001196.4(BID):c.-23G>A	BID (R39Q)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2274938	NM_001196.4(BID):c.-33G>A	BID (G36R)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3133991	NM_001196.4(BID):c.-59+744C>A	BID (A18D)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2552476	NM_001196.4(BID):c.-59+723G>T	BID (R11L)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3133993	NM_001196.4(BID):c.-59+698A>G	BID (S3G)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance

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Items: 24