Product Details
- SNP ID
-
rs3095726
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:37738923 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- CATACCTTACATTCATAGGGTTTCA[C/T]ACCAGTATGAATTTTCTGATGTTGA
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF573
PubMed Links
Gene Details
- Gene
- ZNF573
- Gene Name
- zinc finger protein 573
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001172689.1 |
1503 |
Missense Mutation |
ATG,GTG |
M435V |
NP_001166160.1 |
NM_001172690.1 |
1503 |
Missense Mutation |
ATG,GTG |
M523V |
NP_001166161.1 |
NM_001172691.1 |
1503 |
Missense Mutation |
ATG,GTG |
M521V |
NP_001166162.1 |
NM_001172692.1 |
1503 |
Missense Mutation |
ATG,GTG |
M435V |
NP_001166163.1 |
NM_152360.3 |
1503 |
Missense Mutation |
ATG,GTG |
M465V |
NP_689573.3 |
XM_011526446.2 |
1503 |
Missense Mutation |
ATG,GTG |
M538V |
XP_011524748.1 |
XM_017026275.1 |
1503 |
Missense Mutation |
ATG,GTG |
M538V |
XP_016881764.1 |
XM_017026276.1 |
1503 |
Missense Mutation |
ATG,GTG |
M538V |
XP_016881765.1 |
XM_017026277.1 |
1503 |
Missense Mutation |
ATG,GTG |
M536V |
XP_016881766.1 |
XM_017026278.1 |
1503 |
Missense Mutation |
ATG,GTG |
M467V |
XP_016881767.1 |
XM_017026279.1 |
1503 |
Missense Mutation |
ATG,GTG |
M467V |
XP_016881768.1 |
XM_017026280.1 |
1503 |
Missense Mutation |
ATG,GTG |
M435V |
XP_016881769.1 |
XM_017026281.1 |
1503 |
Missense Mutation |
ATG,GTG |
M435V |
XP_016881770.1 |
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