Product Details

SNP ID
rs74411528
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:17226991 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACGCCTGTGTGGCAAATCAAATCAG[A/G]ATATTCAGCTTCTGTTTCTCACAAA
Phenotype
MIM: 604913
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CNOT7 PubMed Links

Gene Details

Gene
CNOT7
Gene Name
CCR4-NOT transcription complex subunit 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001322087.1 5023 Intron NP_001309016.1
NM_001322088.1 5023 Intron NP_001309017.1
NM_001322089.1 5023 Intron NP_001309018.1
NM_001322090.1 5023 Intron NP_001309019.1
NM_001322091.1 5023 Intron NP_001309020.1
NM_001322092.1 5023 Intron NP_001309021.1
NM_001322093.1 5023 Intron NP_001309022.1
NM_001322094.1 5023 Intron NP_001309023.1
NM_001322095.1 5023 Intron NP_001309024.1
NM_001322096.1 5023 Intron NP_001309025.1
NM_001322097.1 5023 Intron NP_001309026.1
NM_001322098.1 5023 Intron NP_001309027.1
NM_001322099.1 5023 Intron NP_001309028.1
NM_001322100.1 5023 Intron NP_001309029.1
NM_013354.6 5023 Intron NP_037486.2
NM_054026.3 5023 Intron NP_473367.2
XM_005273481.2 5023 UTR 3 XP_005273538.1
Gene
ZDHHC2
Gene Name
zinc finger DHHC-type containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_016353.4 5023 Intron NP_057437.1

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