Product Details

SNP ID
rs739999
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.16:269512 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CACTGCCTGGGCTCACCGTCTCTTC[A/G]TCTCCAGCGGGATCCCAGCCTCTGC
Phenotype
MIM: 603895
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
FAM234A PubMed Links

Gene Details

Gene
FAM234A
Gene Name
family with sequence similarity 234 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001284497.1 1279 Intron NP_001271426.1
NM_032039.3 1279 Intron NP_114428.1
XM_005255622.1 1279 Intron XP_005255679.1
XM_005255623.2 1279 Intron XP_005255680.1
XM_006720957.1 1279 Intron XP_006721020.1
XM_011522691.1 1279 Intron XP_011520993.1
XM_011522692.1 1279 Intron XP_011520994.1
XM_017023760.1 1279 Intron XP_016879249.1
XM_017023761.1 1279 Intron XP_016879250.1
XM_017023762.1 1279 Intron XP_016879251.1
XM_017023763.1 1279 Intron XP_016879252.1
XM_017023764.1 1279 Intron XP_016879253.1
XM_017023765.1 1279 Intron XP_016879254.1
Gene
RGS11
Gene Name
regulator of G-protein signaling 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286485.1 1279 Missense Mutation ACG,ATG T416M NP_001273414.1
NM_001286486.1 1279 Missense Mutation ACG,ATG T243M NP_001273415.1
NM_003834.2 1279 Missense Mutation ACG,ATG T406M NP_003825.1
NM_183337.2 1279 Missense Mutation ACG,ATG T427M NP_899180.1
XM_011522719.2 1279 Missense Mutation ACG,ATG T459M XP_011521021.1
XM_011522720.2 1279 Missense Mutation ACG,ATG T438M XP_011521022.1
XM_011522721.1 1279 Intron XP_011521023.1
XM_011522722.1 1279 Intron XP_011521024.1
XM_011522723.1 1279 Intron XP_011521025.1

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