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SNP ID: rs201693357
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:49659616 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ATTGGTTGAGGTGGTGGGGAACAGG[C/G]GGGTTGGAGGCACACCATGAGGAGC
Phenotype: MIM: 610837 MIM: 603734
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: BCL2L12 PubMed Links

Gene Details

Gene: BCL2L12
Gene Name: BCL2 like 12

There are no transcripts associated with this gene.

Gene: IRF3
Gene Name: interferon regulatory factor 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001197122.1	1627	Silent Mutation	CCC,CCG	P444P	NP_001184051.1
NM_001197123.1	1627	UTR 3			NP_001184052.1
NM_001197124.1	1627	UTR 3			NP_001184053.1
NM_001197125.1	1627	UTR 3			NP_001184054.1
NM_001197126.1	1627	UTR 3			NP_001184055.1
NM_001197127.1	1627	UTR 3			NP_001184056.1
NM_001197128.1	1627	UTR 3			NP_001184057.1
NM_001571.5	1627	UTR 3			NP_001562.1
XM_006723197.1	1627	Silent Mutation	CCC,CCG	P444P	XP_006723260.1
XM_006723198.1	1627	Silent Mutation	CCC,CCG	P444P	XP_006723261.1
XM_006723200.1	1627	Silent Mutation	CCC,CCG	P409P	XP_006723263.1
XM_006723201.1	1627	Silent Mutation	CCC,CCG	P298P	XP_006723264.1
XM_006723202.2	1627	Silent Mutation	CCC,CCG	P298P	XP_006723265.1
XM_017026766.1	1627	UTR 3			XP_016882255.1
XM_017026767.1	1627	UTR 3			XP_016882256.1

Gene: SCAF1
Gene Name: SR-related CTD associated factor 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021228.2	1627	Intron			NP_067051.2
XM_005259122.4	1627	Intron			XP_005259179.1
XM_011527194.2	1627	Intron			XP_011525496.1
XM_017027083.1	1627	Intron			XP_016882572.1

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