Product Details

SNP ID

rs956748

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:119732109 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGGTGGTCACTGTGTTTGGAGGCTG[C/T]AGATTCCTTAGTAAAGACTGAGAGT

Phenotype

MIM: 604912

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TAF2 PubMed Links

Gene Details

Gene

TAF2

Gene Name

TATA-box binding protein associated factor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003184.3	3551	Missense Mutation	ACA,GCA	T1139A	NP_003175.1
XM_006716621.3	3551	Missense Mutation	ACA,GCA	T1191A	XP_006716684.1
XM_011517259.2	3551	Missense Mutation	ACA,GCA	T1154A	XP_011515561.1
XM_017013779.1	3551	Missense Mutation	ACA,GCA	T1102A	XP_016869268.1
XM_017013780.1	3551	Missense Mutation	ACA,GCA	T1022A	XP_016869269.1
XM_017013781.1	3551	Missense Mutation	ACA,GCA	T1022A	XP_016869270.1
XM_017013782.1	3551	Missense Mutation	ACA,GCA	T1022A	XP_016869271.1
XM_017013783.1	3551	Missense Mutation	ACA,GCA	T980A	XP_016869272.1
XM_017013784.1	3551	Missense Mutation	ACA,GCA	T970A	XP_016869273.1
XM_017013785.1	3551	Missense Mutation	ACA,GCA	T970A	XP_016869274.1
XM_017013786.1	3551	Missense Mutation	ACA,GCA	T970A	XP_016869275.1
XM_017013787.1	3551	Missense Mutation	ACA,GCA	T933A	XP_016869276.1
XM_017013788.1	3551	Missense Mutation	ACA,GCA	T774A	XP_016869277.1
XM_017013789.1	3551	Missense Mutation	ACA,GCA	T722A	XP_016869278.1
XM_017013790.1	3551	Missense Mutation	ACA,GCA	T722A	XP_016869279.1
XM_017013791.1	3551	Missense Mutation	ACA,GCA	T692A	XP_016869280.1

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