Product Details

SNP ID
rs149633716
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:23357511 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTGCTGTGGGGCACGAAAAGGCG[C/T]GGGGGCTGATTAGCCTGGGTACTGG
Phenotype
MIM: 609906 MIM: 611461
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
EFS PubMed Links

Gene Details

Gene
EFS
Gene Name
embryonal Fyn-associated substrate
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001277174.1 1502 Silent Mutation CCC,CCT P298P NP_001264103.1
NM_005864.3 1502 Silent Mutation CCC,CCT P467P NP_005855.1
NM_032459.2 1502 Silent Mutation CCC,CCT P374P NP_115835.1
XM_005267256.1 1502 Silent Mutation CCC,CCT P437P XP_005267313.1
Gene
SLC22A17
Gene Name
solute carrier family 22 member 17
There are no transcripts associated with this gene.

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