Product Details

SNP ID
rs79595086
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:1886071 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGTTGAAGCATATTTTCTGCTTAT[A/C]TTTTCCTTTACGAAACTAAAGCGCG
Phenotype
MIM: 602952
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
WHSC1 PubMed Links

Gene Details

Gene
WHSC1
Gene Name
Wolf-Hirschhorn syndrome candidate 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001042424.2 Intron NP_001035889.1
NM_007331.1 Intron NP_015627.1
NM_133330.2 Intron NP_579877.1
NM_133331.2 Intron NP_579878.1
NM_133334.2 Intron NP_579889.1
NM_133335.3 Intron NP_579890.1
XM_005248001.3 Intron XP_005248058.1
XM_005248002.2 Intron XP_005248059.1
XM_005248005.2 Intron XP_005248062.1
XM_006713914.3 Intron XP_006713977.1
XM_011513557.2 Intron XP_011511859.1
XM_011513560.2 Intron XP_011511862.1
XM_017008587.1 Intron XP_016864076.1
XM_017008588.1 Intron XP_016864077.1

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