Product Details
- SNP ID
-
rs58594363
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:9653771 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGTCTTTTCCATAACAATTACCCTC[A/C]AAAGTGTTCCCTCCATTCTGAGCTC
- Phenotype
-
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF562
PubMed Links
Gene Details
- Gene
- ZNF562
- Gene Name
- zinc finger protein 562
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001130031.1 |
811 |
Missense Mutation |
TTG,TTT |
L153F |
NP_001123503.1 |
NM_001130032.1 |
811 |
Missense Mutation |
TTG,TTT |
L153F |
NP_001123504.1 |
NM_001300885.1 |
811 |
Missense Mutation |
TTG,TTT |
L152F |
NP_001287814.1 |
NM_017656.3 |
811 |
Missense Mutation |
TTG,TTT |
L81F |
NP_060126.2 |
XM_005259941.3 |
811 |
Missense Mutation |
TTG,TTT |
L153F |
XP_005259998.1 |
XM_005259944.3 |
811 |
Missense Mutation |
TTG,TTT |
L116F |
XP_005260001.1 |
XM_005259951.3 |
811 |
Missense Mutation |
TTG,TTT |
L37F |
XP_005260008.1 |
XM_005259952.3 |
811 |
Missense Mutation |
TTG,TTT |
L10F |
XP_005260009.1 |
XM_011528100.2 |
811 |
Missense Mutation |
TTG,TTT |
L84F |
XP_011526402.1 |
XM_011528102.2 |
811 |
Missense Mutation |
TTG,TTT |
L38F |
XP_011526404.1 |
XM_017026898.1 |
811 |
Missense Mutation |
TTG,TTT |
L152F |
XP_016882387.1 |
XM_017026899.1 |
811 |
Missense Mutation |
TTG,TTT |
L10F |
XP_016882388.1 |
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