Product Details
- SNP ID
-
rs200609597
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:144773720 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGGTTTCTCTCCAGTGTGAATTCTC[C/T]GATGTTGGATAAGGTTAGAACTTTG
- Phenotype
-
MIM: 194526
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF34
PubMed Links
Gene Details
- Gene
- ZNF34
- Gene Name
- zinc finger protein 34
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001286769.1 |
1340 |
Missense Mutation |
CAG,CGG |
Q389R |
NP_001273698.1 |
NM_001286770.1 |
1340 |
Missense Mutation |
CAG,CGG |
Q370R |
NP_001273699.1 |
NM_030580.4 |
1340 |
Missense Mutation |
CAG,CGG |
Q410R |
NP_085057.3 |
XM_011517314.2 |
1340 |
Missense Mutation |
CAG,CGG |
Q410R |
XP_011515616.1 |
XM_011517315.2 |
1340 |
Missense Mutation |
CAG,CGG |
Q389R |
XP_011515617.1 |
XM_011517316.2 |
1340 |
Missense Mutation |
CAG,CGG |
Q389R |
XP_011515618.1 |
XM_011517318.2 |
1340 |
Missense Mutation |
CAG,CGG |
Q389R |
XP_011515620.1 |
XM_011517320.2 |
1340 |
Missense Mutation |
CAG,CGG |
Q349R |
XP_011515622.1 |
XM_017013872.1 |
1340 |
Missense Mutation |
CAG,CGG |
Q410R |
XP_016869361.1 |
XM_017013873.1 |
1340 |
Missense Mutation |
CAG,CGG |
Q410R |
XP_016869362.1 |
XM_017013874.1 |
1340 |
Missense Mutation |
CAG,CGG |
Q410R |
XP_016869363.1 |
XM_017013875.1 |
1340 |
Missense Mutation |
CAG,CGG |
Q389R |
XP_016869364.1 |
XM_017013876.1 |
1340 |
Missense Mutation |
CAG,CGG |
Q349R |
XP_016869365.1 |
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