Product Details

SNP ID
rs1726129
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:111661174 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGGTCCCGCAGCTTGGTGGCTCAGG[C/G]CGGCCACAGTCTCCACATTAGCACC
Phenotype
MIM: 137025
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
FYN PubMed Links

Gene Details

Gene
FYN
Gene Name
FYN proto-oncogene, Src family tyrosine kinase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002037.5 2282 UTR 3 NP_002028.1
NM_153047.3 2282 UTR 3 NP_694592.1
NM_153048.3 2282 UTR 3 NP_694593.1
XM_005266890.3 2282 UTR 3 XP_005266947.1
XM_005266892.3 2282 UTR 3 XP_005266949.1
XM_017010650.1 2282 UTR 3 XP_016866139.1
XM_017010651.1 2282 UTR 3 XP_016866140.1
XM_017010652.1 2282 UTR 3 XP_016866141.1
XM_017010653.1 2282 UTR 3 XP_016866142.1
XM_017010654.1 2282 UTR 3 XP_016866143.1
XM_017010655.1 2282 Intron XP_016866144.1

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