Product Details

SNP ID
rs362298
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:3244212 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGCTTCTGCAAGGGCCTTCCCAAA[C/G]CACAGTACAGGTGGTCTTCCTGCCC
Phenotype
MIM: 613004
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
HTT PubMed Links

Gene Details

Gene
HTT
Gene Name
huntingtin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002111.8 485 Intron NP_002102.4
Gene
MSANTD1
Gene Name
Myb/SANT DNA binding domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001042690.1 485 Intron NP_001036155.1
XM_011513465.2 485 UTR 5 XP_011511767.1
XM_011513466.2 485 UTR 5 XP_011511768.1
XM_011513467.2 485 UTR 5 XP_011511769.1
XM_017008169.1 485 UTR 5 XP_016863658.1

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