Product Details
- SNP ID
-
rs200843141
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:47066768 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTCAGCACCCTTGGGCTGGGCACCC[A/G]TGTCAGCAGCCGGCTCTGTGGCTTT
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZC3H4
PubMed Links
Gene Details
- Gene
- ZC3H4
- Gene Name
- zinc finger CCCH-type containing 4
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_015168.1 |
4813 |
Missense Mutation |
ACG,ATG |
T1167M |
NP_055983.1 |
XM_005258676.3 |
4813 |
Missense Mutation |
ACG,ATG |
T1131M |
XP_005258733.1 |
XM_005258677.4 |
4813 |
Missense Mutation |
ACG,ATG |
T1126M |
XP_005258734.1 |
XM_005258678.2 |
4813 |
Missense Mutation |
ACG,ATG |
T1118M |
XP_005258735.1 |
XM_006723113.3 |
4813 |
Missense Mutation |
ACG,ATG |
T1167M |
XP_006723176.1 |
XM_011526668.2 |
4813 |
Missense Mutation |
ACG,ATG |
T1126M |
XP_011524970.1 |
XM_011526669.2 |
4813 |
Missense Mutation |
ACG,ATG |
T1121M |
XP_011524971.1 |
XM_011526670.2 |
4813 |
Missense Mutation |
ACG,ATG |
T1117M |
XP_011524972.1 |
XM_017026529.1 |
4813 |
Missense Mutation |
ACG,ATG |
T1154M |
XP_016882018.1 |
XM_017026530.1 |
4813 |
Missense Mutation |
ACG,ATG |
T1083M |
XP_016882019.1 |
XM_017026531.1 |
4813 |
Missense Mutation |
ACG,ATG |
T870M |
XP_016882020.1 |
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