Product Details
- SNP ID
-
rs62619253
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:3360139 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTTCTCTCCAGTGTCAATGTTCTCA[C/G]GTTCAGTAAAGTGTGAGCACTGGAT
- Phenotype
-
MIM: 602187
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF195
PubMed Links
Gene Details
- Gene
- ZNF195
- Gene Name
- zinc finger protein 195
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001130519.2 |
1388 |
Missense Mutation |
CCT,CGT |
P267R |
NP_001123991.1 |
NM_001130520.2 |
1388 |
Missense Mutation |
CCT,CGT |
P290R |
NP_001123992.1 |
NM_001242841.1 |
1388 |
Missense Mutation |
CCT,CGT |
P271R |
NP_001229770.1 |
NM_001242842.1 |
1388 |
Missense Mutation |
CCT,CGT |
P245R |
NP_001229771.1 |
NM_001242843.1 |
1388 |
Missense Mutation |
CCT,CGT |
P222R |
NP_001229772.1 |
NM_001256823.1 |
1388 |
UTR 3 |
|
|
NP_001243752.1 |
NM_001256824.1 |
1388 |
Missense Mutation |
CCT,CGT |
P253R |
NP_001243753.1 |
NM_001256825.1 |
1388 |
Missense Mutation |
CCT,CGT |
P222R |
NP_001243754.1 |
NM_007152.4 |
1388 |
Missense Mutation |
CCT,CGT |
P218R |
NP_009083.2 |
XM_006718306.1 |
1388 |
Missense Mutation |
CCT,CGT |
P233R |
XP_006718369.1 |
XM_011520350.2 |
1388 |
Missense Mutation |
CCT,CGT |
P294R |
XP_011518652.1 |
XM_011520351.2 |
1388 |
Missense Mutation |
CCT,CGT |
P294R |
XP_011518653.1 |
XM_011520352.2 |
1388 |
Missense Mutation |
CCT,CGT |
P256R |
XP_011518654.1 |
XM_011520354.2 |
1388 |
Intron |
|
|
XP_011518656.2 |
XM_017018260.1 |
1388 |
Missense Mutation |
CCT,CGT |
P305R |
XP_016873749.1 |
XM_017018261.1 |
1388 |
Missense Mutation |
CCT,CGT |
P294R |
XP_016873750.1 |
XM_017018262.1 |
1388 |
Missense Mutation |
CCT,CGT |
P282R |
XP_016873751.1 |
XM_017018263.1 |
1388 |
Missense Mutation |
CCT,CGT |
P271R |
XP_016873752.1 |
XM_017018264.1 |
1388 |
Missense Mutation |
CCT,CGT |
P150R |
XP_016873753.1 |
XM_017018265.1 |
1388 |
Missense Mutation |
CCT,CGT |
P191R |
XP_016873754.1 |
XM_017018266.1 |
1388 |
Missense Mutation |
CCT,CGT |
P191R |
XP_016873755.1 |
XM_017018267.1 |
1388 |
Missense Mutation |
CCT,CGT |
P214R |
XP_016873756.1 |
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