Product Details
- SNP ID
-
rs200516733
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:36449921 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAATCACGTCTTGTGAGTTTTTCCA[C/T]TATTTCCCACTGGGTTGATTCTATT
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF566
PubMed Links
Gene Details
- Gene
- ZNF566
- Gene Name
- zinc finger protein 566
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001145343.1 |
662 |
Missense Mutation |
ATG,GTG |
M106V |
NP_001138815.1 |
NM_001145344.1 |
662 |
Missense Mutation |
ATG,GTG |
M105V |
NP_001138816.1 |
NM_001145345.1 |
662 |
Missense Mutation |
ATG,GTG |
M105V |
NP_001138817.1 |
NM_001300970.1 |
662 |
Missense Mutation |
ATG,GTG |
M1V |
NP_001287899.1 |
NM_032838.4 |
662 |
Missense Mutation |
ATG,GTG |
M105V |
NP_116227.1 |
XM_005259354.2 |
662 |
Missense Mutation |
ATG,GTG |
M73V |
XP_005259411.1 |
XM_005259356.2 |
662 |
Missense Mutation |
ATG,GTG |
M1V |
XP_005259413.1 |
XM_006723447.2 |
662 |
Missense Mutation |
ATG,GTG |
M106V |
XP_006723510.1 |
XM_011527428.1 |
662 |
Missense Mutation |
ATG,GTG |
M1V |
XP_011525730.1 |
XM_017027399.1 |
662 |
Missense Mutation |
ATG,GTG |
M1V |
XP_016882888.1 |
XM_017027400.1 |
662 |
Missense Mutation |
ATG,GTG |
M1V |
XP_016882889.1 |
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