Product Details

SNP ID
rs28763975
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:111661835 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTCAAAAGTGGGGCGTTCTTCAGG[C/G]TCCTTTTTCCAGCAGTGGATCATGA
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 1621 Silent Mutation GAC,GAG D506E NP_002028.1
NM_153047.3 1621 Silent Mutation GAC,GAG D503E NP_694592.1
NM_153048.3 1621 Silent Mutation GAC,GAG D451E NP_694593.1
XM_005266890.3 1621 Silent Mutation GAC,GAG D503E XP_005266947.1
XM_005266892.3 1621 Silent Mutation GAC,GAG D451E XP_005266949.1
XM_017010650.1 1621 Missense Mutation GAC,GAG D506E XP_016866139.1
XM_017010651.1 1621 Silent Mutation GAC,GAG D506E XP_016866140.1
XM_017010652.1 1621 Silent Mutation GAC,GAG D506E XP_016866141.1
XM_017010653.1 1621 Silent Mutation GAC,GAG D506E XP_016866142.1
XM_017010654.1 1621 Silent Mutation GAC,GAG D506E XP_016866143.1
XM_017010655.1 1621 Intron XP_016866144.1

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