BIRC5[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3134029	NM_001168.3(BIRC5):c.23C>T (p.Pro8Leu)	BIRC5 (P8L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620882	NM_001168.3(BIRC5):c.76C>A (p.Pro26Thr)	BIRC5 (P26T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134028	NM_001168.3(BIRC5):c.222-682G>A	BIRC5 (A80T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249326	NM_001168.3(BIRC5):c.222-671T>G	BIRC5 (C83W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2681538	NM_001168.3(BIRC5):c.222-667A>C	BIRC5 (T85P)	Single nucleotide variant (missense variant +1 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2487858	NM_001168.3(BIRC5):c.222-664A>T	BIRC5 (S86C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2681528	NM_001168.3(BIRC5):c.222-639G>A	BIRC5 (R94Q)	Single nucleotide variant (missense variant +1 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2382232	NM_001168.3(BIRC5):c.242C>T (p.Ser81Leu)	BIRC5 (S81L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2412098	NM_001168.3(BIRC5):c.247G>A (p.Gly83Ser)	BIRC5 (G83S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3134030	NM_001168.3(BIRC5):c.253G>T (p.Ala85Ser)	BIRC5 (A108S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2648338	NM_001168.3(BIRC5):c.315C>T (p.Asp105=)	BIRC5	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3024828	NM_001168.3(BIRC5):c.340-638G>A	BIRC5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3134031	NM_001168.3(BIRC5):c.355A>C (p.Asn119His)	BIRC5 (N142H +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3134032	NM_001168.3(BIRC5):c.394C>T (p.Arg132Cys)	BIRC5 (R155C +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2462715	NM_001168.3(BIRC5):c.397C>T (p.Arg133Cys)	BIRC5 (R133C +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2530560	NM_001168.3(BIRC5):c.398G>A (p.Arg133His)	BIRC5 (R133H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221943	NM_001168.3(BIRC5):c.406G>A (p.Glu136Lys)	BIRC5 (E159K +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2648339	NM_001168.3(BIRC5):c.*50G>C	BIRC5 (G121R)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign