Product Details
- SNP ID
-
rs201010345
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:36639455 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTCTTTACATTCATAAGGTTTCTCA[C/T]CAGTGTGAATTCTTTGATGTAGAGT
- Phenotype
-
MIM: 608640
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF461
PubMed Links
Gene Details
- Gene
- ZNF461
- Gene Name
- zinc finger protein 461
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001297623.2 |
1097 |
Missense Mutation |
GAT,GGT |
D274G |
NP_001284552.1 |
NM_001322821.1 |
1097 |
Missense Mutation |
GAT,GGT |
D291G |
NP_001309750.1 |
NM_001322823.1 |
1097 |
Missense Mutation |
GAT,GGT |
D266G |
NP_001309752.1 |
NM_001322825.1 |
1097 |
Missense Mutation |
GAT,GGT |
D266G |
NP_001309754.1 |
NM_001322826.1 |
1097 |
Missense Mutation |
GAT,GGT |
D243G |
NP_001309755.1 |
NM_001322827.1 |
1097 |
Missense Mutation |
GAT,GGT |
D243G |
NP_001309756.1 |
NM_001322828.1 |
1097 |
Missense Mutation |
GAT,GGT |
D209G |
NP_001309757.1 |
NM_153257.4 |
1097 |
Missense Mutation |
GAT,GGT |
D297G |
NP_694989.2 |
XM_011527486.2 |
1097 |
Missense Mutation |
GAT,GGT |
D170G |
XP_011525788.1 |
XM_017027470.1 |
1097 |
Missense Mutation |
GAT,GGT |
D253G |
XP_016882959.1 |
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