Product Details

SNP ID
rs201910975
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:205228634 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAGGATGGAGCTGGGCTGGAAGAT[A/G]CCGCTTCCCACCTGCCGGGCGCGGA
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TMCC2 PubMed Links

Gene Details

Gene
TMCC2
Gene Name
transmembrane and coiled-coil domain family 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001242925.1 725 Intron NP_001229854.1
NM_001297611.1 725 Intron NP_001284540.1
NM_001297613.1 725 Intron NP_001284542.1
NM_014858.3 725 Missense Mutation ACC,GCC T24A NP_055673.2
XM_005245684.1 725 Intron XP_005245741.1
XM_005245685.4 725 Intron XP_005245742.1
XM_005245686.3 725 Missense Mutation ACC,GCC T24A XP_005245743.1
XM_017003000.1 725 Intron XP_016858489.1

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