Product Details

SNP ID
rs180754888
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:46500505 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCTTCTCATCAGAGGCTTTCCCAT[G/T]TTCACTGCACTGAGGTTTCTCACTT
Phenotype
MIM: 300573
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
ZNF674 PubMed Links

Gene Details

Gene
ZNF674
Gene Name
zinc finger protein 674
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039891.2 1482 Missense Mutation AAT,CAT N362H NP_001034980.1
NM_001146291.1 1482 Missense Mutation AAT,CAT N356H NP_001139763.1
NM_001190417.1 1482 Missense Mutation AAT,CAT N357H NP_001177346.1
XM_011543941.2 1482 Intron XP_011542243.1
XM_011543943.2 1482 Intron XP_011542245.1
XM_011543944.2 1482 Intron XP_011542246.1
XM_011543945.2 1482 Intron XP_011542247.1
XM_017029728.1 1482 Intron XP_016885217.1
XM_017029729.1 1482 Intron XP_016885218.1
XM_017029730.1 1482 Missense Mutation AAT,CAT N295H XP_016885219.1
XM_017029731.1 1482 Intron XP_016885220.1
XM_017029732.1 1482 Intron XP_016885221.1
XM_017029733.1 1482 Intron XP_016885222.1

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