Product Details

SNP ID

rs149807206

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:89883378 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAACATTGACGATCTTGAGGATGAC[C/G]CTGTGGTGAACGGGGAGAGGTCTGG

Phenotype

MIM: 612326

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

TCF25 PubMed Links

Gene Details

Gene

TCF25

Gene Name

transcription factor 25

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014972.2	903	Missense Mutation	CCT,GCT	P74A	NP_055787.1
XM_005256297.2	903	Missense Mutation	CCT,GCT	P74A	XP_005256354.1
XM_005256298.2	903	Missense Mutation	CCT,GCT	P74A	XP_005256355.1
XM_005256299.2	903	Missense Mutation	CCT,GCT	P74A	XP_005256356.1
XM_011522956.2	903	Missense Mutation	CCT,GCT	P74A	XP_011521258.1
XM_011522957.2	903	Missense Mutation	CCT,GCT	P74A	XP_011521259.1
XM_011522958.2	903	Missense Mutation	CCT,GCT	P74A	XP_011521260.1
XM_011522959.2	903	Missense Mutation	CCT,GCT	P74A	XP_011521261.1
XM_011522960.2	903	Missense Mutation	CCT,GCT	P74A	XP_011521262.1
XM_011522961.2	903	UTR 5			XP_011521263.1
XM_017023047.1	903	Missense Mutation	CCT,GCT	P74A	XP_016878536.1
XM_017023048.1	903	Missense Mutation	CCT,GCT	P74A	XP_016878537.1
XM_017023049.1	903	Missense Mutation	CCT,GCT	P74A	XP_016878538.1
XM_017023050.1	903	Missense Mutation	CCT,GCT	P74A	XP_016878539.1
XM_017023051.1	903	Missense Mutation	CCT,GCT	P74A	XP_016878540.1
XM_017023052.1	903	Missense Mutation	CCT,GCT	P74A	XP_016878541.1
XM_017023053.1	903	UTR 5			XP_016878542.1
XM_017023054.1	903	UTR 5			XP_016878543.1
XM_017023055.1	903	UTR 5			XP_016878544.1
XM_017023056.1	903	UTR 5			XP_016878545.1
XM_017023057.1	903	UTR 5			XP_016878546.1
XM_017023058.1	903	UTR 5			XP_016878547.1

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