Product Details

SNP ID
rs149966729
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:51095264 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTACTTCAGTATGATATGATAGC[C/T]ATCATTGGTTTCTGCTGTTAAAAAA
Phenotype
MIM: 189889
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TFCP2 PubMed Links

Gene Details

Gene
TFCP2
Gene Name
transcription factor CP2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001173452.1 2207 Missense Mutation AGC,GGC S495G NP_001166923.1
NM_001173453.1 2207 Missense Mutation AGC,GGC S444G NP_001166924.1
NM_005653.4 2207 Missense Mutation AGC,GGC S496G NP_005644.2

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