Product Details

SNP ID
rs200981269
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:15779137 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACAACTGCAGTCCCTTCTACGTAC[A/C]TGACCTGTTGAACAAAATAAAGCCA
Phenotype
MIM: 611649
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
FAM188A PubMed Links

Gene Details

Gene
FAM188A
Gene Name
family with sequence similarity 188 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318330.1 1413 Missense Mutation NP_001305259.1
NM_024948.3 1413 Missense Mutation NP_079224.1
XM_005252600.2 1413 Missense Mutation XP_005252657.1
XM_005252602.2 1413 Missense Mutation XP_005252659.1
XM_006717508.2 1413 Missense Mutation XP_006717571.1
XM_011519690.2 1413 Intron XP_011517992.1
XM_011519691.2 1413 Intron XP_011517993.1
XM_011519693.1 1413 Missense Mutation XP_011517995.1
XM_011519694.1 1413 Missense Mutation XP_011517996.1
XM_017016671.1 1413 Intron XP_016872160.1
XM_017016672.1 1413 Missense Mutation XP_016872161.1
XM_017016673.1 1413 Missense Mutation XP_016872162.1
XM_017016674.1 1413 Missense Mutation XP_016872163.1
XM_017016675.1 1413 Missense Mutation XP_016872164.1
XM_017016676.1 1413 Missense Mutation XP_016872165.1

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