Product Details

SNP ID
rs201903938
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:93937757 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGTCGATGTGTTCCTTCAGCCGC[C/G]AGCAGAGCTGCACGTTGCCCACGTA
Phenotype
MIM: 605759
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
ASB2 PubMed Links

Gene Details

Gene
ASB2
Gene Name
ankyrin repeat and SOCS box containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001202429.1 1992 Missense Mutation TCG,TGG S571W NP_001189358.1
NM_016150.4 1992 Missense Mutation TCG,TGG S523W NP_057234.2
XM_005267758.3 1992 Missense Mutation TCG,TGG S571W XP_005267815.1
XM_011536834.2 1992 Missense Mutation TCG,TGG S519W XP_011535136.1
XM_011536835.2 1992 Missense Mutation TCG,TGG S469W XP_011535137.1
XM_017021369.1 1992 Missense Mutation TCG,TGG S536W XP_016876858.1
Gene
FAM181A
Gene Name
family with sequence similarity 181 member A
There are no transcripts associated with this gene.

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