"Ambry Genetics"[submitter] AND "SERINC1"[gene] - ClinVar

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

Search results

Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3317520	NM_020755.4(SERINC1):c.1270T>G (p.Trp424Gly)	SERINC1 (W424G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160244	NM_020755.4(SERINC1):c.1240C>A (p.Arg414Ser)	SERINC1 (R414S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356543	NM_020755.4(SERINC1):c.1217A>G (p.Asn406Ser)	SERINC1 (N406S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207476	NM_020755.4(SERINC1):c.1208C>T (p.Thr403Ile)	SERINC1 (T403I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317524	NM_020755.4(SERINC1):c.1107C>T (p.Asp369=)	SERINC1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2226078	NM_020755.4(SERINC1):c.1075G>A (p.Ala359Thr)	SERINC1 (A359T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321343	NM_020755.4(SERINC1):c.977T>G (p.Leu326Trp)	SERINC1 (L326W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343165	NM_020755.4(SERINC1):c.946C>A (p.Gln316Lys)	SERINC1 (Q316K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519046	NM_020755.4(SERINC1):c.915G>C (p.Lys305Asn)	SERINC1 (K305N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366397	NM_020755.4(SERINC1):c.656A>C (p.Tyr219Ser)	SERINC1 (Y219S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525167	NM_020755.4(SERINC1):c.640G>A (p.Val214Ile)	SERINC1 (V214I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403195	NM_020755.4(SERINC1):c.456G>C (p.Trp152Cys)	SERINC1 (W152C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160245	NM_020755.4(SERINC1):c.275G>A (p.Arg92His)	SERINC1 (R92H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346829	NM_020755.4(SERINC1):c.257G>T (p.Gly86Val)	SERINC1 (G86V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317523	NM_020755.4(SERINC1):c.158C>T (p.Ala53Val)	SERINC1 (A53V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341160	NM_020755.4(SERINC1):c.154G>A (p.Val52Ile)	SERINC1 (V52I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160246	NM_020755.4(SERINC1):c.86G>A (p.Cys29Tyr)	SERINC1 (C29Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554421	NM_020755.4(SERINC1):c.74T>C (p.Leu25Pro)	SERINC1 (L25P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487107	NM_020755.4(SERINC1):c.62C>T (p.Ala21Val)	SERINC1 (A21V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317521	NM_020755.4(SERINC1):c.14T>C (p.Leu5Pro)	LOC129997092, SERINC1 (L5P)	Single nucleotide variant (missense variant)	not specified	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: 20