Product Details

SNP ID
rs148537880
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:13088844 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATGGGCCTTGCAACGTGGCAAATT[C/T]CAGTAGTCCTTTCTCACCTCTCTTG
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM234B PubMed Links

Gene Details

Gene
FAM234B
Gene Name
family with sequence similarity 234 member B
There are no transcripts associated with this gene.

Gene
GSG1
Gene Name
germ cell associated 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080554.2 654 Missense Mutation AAA,GAA K167E NP_001074023.1
NM_001080555.2 654 Intron NP_001074024.1
NM_001206842.1 654 Intron NP_001193771.1
NM_001206843.1 654 Intron NP_001193772.1
NM_001206845.1 654 Intron NP_001193774.1
NM_031289.3 654 Missense Mutation AAA,GAA K131E NP_112579.2
NM_153823.3 654 Intron NP_722545.2
XM_005253493.2 654 Intron XP_005253550.1
XM_005253495.1 654 Missense Mutation AAA,GAA K191E XP_005253552.1
XM_011520858.1 654 Intron XP_011519160.1
XM_011520859.1 654 Intron XP_011519161.1
XM_011520860.1 654 Missense Mutation AAA,GAA K191E XP_011519162.1
XM_011520861.1 654 Intron XP_011519163.1
XM_011520862.1 654 Missense Mutation AAA,GAA K167E XP_011519164.1
XM_011520863.1 654 Missense Mutation AAA,GAA K144E XP_011519165.1

View Full Product Details