Product Details
- SNP ID
-
rs147989825
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:43366935 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTTGCCTTCTCCTTCCCGCTTTCCA[C/T]TGGTTCCTCCTTCAGGTTCTCGGTC
- Phenotype
-
MIM: 613726
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ANO10
PubMed Links
Gene Details
- Gene
- ANO10
- Gene Name
- anoctamin 10
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001204831.1 |
1962 |
UTR 3 |
|
|
NP_001191760.1 |
NM_001204832.1 |
1962 |
Missense Mutation |
ATG,GTG |
M586V |
NP_001191761.1 |
NM_001204833.1 |
1962 |
Missense Mutation |
ATG,GTG |
M541V |
NP_001191762.1 |
NM_001204834.1 |
1962 |
Missense Mutation |
ATG,GTG |
M462V |
NP_001191763.1 |
NM_018075.3 |
1962 |
Missense Mutation |
ATG,GTG |
M652V |
NP_060545.3 |
XM_011533885.2 |
1962 |
Intron |
|
|
XP_011532187.2 |
XM_011533887.2 |
1962 |
Missense Mutation |
ATG,GTG |
M652V |
XP_011532189.1 |
XM_011533889.2 |
1962 |
Intron |
|
|
XP_011532191.1 |
XM_011533890.2 |
1962 |
Intron |
|
|
XP_011532192.1 |
XM_017006716.1 |
1962 |
Missense Mutation |
ATG,GTG |
M691V |
XP_016862205.1 |
XM_017006717.1 |
1962 |
Missense Mutation |
ATG,GTG |
M691V |
XP_016862206.1 |
XM_017006718.1 |
1962 |
Intron |
|
|
XP_016862207.1 |
XM_017006719.1 |
1962 |
Missense Mutation |
ATG,GTG |
M625V |
XP_016862208.1 |
XM_017006720.1 |
1962 |
Missense Mutation |
ATG,GTG |
M613V |
XP_016862209.1 |
XM_017006721.1 |
1962 |
Missense Mutation |
ATG,GTG |
M586V |
XP_016862210.1 |
XM_017006722.1 |
1962 |
Missense Mutation |
ATG,GTG |
M586V |
XP_016862211.1 |
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