Product Details
- SNP ID
-
rs140423768
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:111661804 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTAAAGTAGTCTTCCAGGAAGCTCT[C/G]CAAGTACTCAAAAGTGGGGCGTTCT
- 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 |
1652 |
Missense Mutation |
CAG,GAG |
Q517E |
NP_002028.1 |
NM_153047.3 |
1652 |
Missense Mutation |
CAG,GAG |
Q514E |
NP_694592.1 |
NM_153048.3 |
1652 |
Missense Mutation |
CAG,GAG |
Q462E |
NP_694593.1 |
XM_005266890.3 |
1652 |
Missense Mutation |
CAG,GAG |
Q514E |
XP_005266947.1 |
XM_005266892.3 |
1652 |
Missense Mutation |
CAG,GAG |
Q462E |
XP_005266949.1 |
XM_017010650.1 |
1652 |
Missense Mutation |
CAG,GAG |
Q517E |
XP_016866139.1 |
XM_017010651.1 |
1652 |
Missense Mutation |
CAG,GAG |
Q517E |
XP_016866140.1 |
XM_017010652.1 |
1652 |
Missense Mutation |
CAG,GAG |
Q517E |
XP_016866141.1 |
XM_017010653.1 |
1652 |
Missense Mutation |
CAG,GAG |
Q517E |
XP_016866142.1 |
XM_017010654.1 |
1652 |
Missense Mutation |
CAG,GAG |
Q517E |
XP_016866143.1 |
XM_017010655.1 |
1652 |
Intron |
|
|
XP_016866144.1 |
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