Product Details
- SNP ID
-
rs183863939
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.16:67539859 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCTCTCCCCCAGCAAGTCAAGTCCA[C/T]TGAACGCTTCCTGCGACGACTGGAG
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FAM65A
PubMed Links
Gene Details
- Gene
- FAM65A
- Gene Name
- family with sequence similarity 65 member A
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001193522.1 |
507 |
Missense Mutation |
ACT,ATT |
T129I |
NP_001180451.1 |
NM_001193523.1 |
507 |
Missense Mutation |
ACT,ATT |
T145I |
NP_001180452.1 |
NM_001193524.1 |
507 |
Missense Mutation |
ACT,ATT |
T139I |
NP_001180453.1 |
NM_024519.3 |
507 |
Missense Mutation |
ACT,ATT |
T125I |
NP_078795.2 |
XM_011523321.1 |
507 |
Missense Mutation |
ACT,ATT |
T145I |
XP_011521623.1 |
XM_011523322.1 |
507 |
Missense Mutation |
ACT,ATT |
T145I |
XP_011521624.1 |
XM_011523324.2 |
507 |
Missense Mutation |
ACT,ATT |
T139I |
XP_011521626.1 |
XM_011523325.1 |
507 |
Missense Mutation |
ACT,ATT |
T125I |
XP_011521627.1 |
XM_011523326.1 |
507 |
Missense Mutation |
ACT,ATT |
T125I |
XP_011521628.1 |
XM_017023663.1 |
507 |
Missense Mutation |
ACT,ATT |
T145I |
XP_016879152.1 |
XM_017023664.1 |
507 |
UTR 5 |
|
|
XP_016879153.1 |
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