Product Details

SNP ID: rs3842753
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.11:2159830 on Build GRCh38
Set Membership: Validated
Context Sequence [VIC/FAM]: CTCTCGGTGCAGGAGGCGGCGGGTG[G/T]GGGGCTGCCTGCGGGCTGCGTCTAG
Phenotype: MIM: 176730 MIM: 191290
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: INS PubMed Links

Gene Details

Gene: INS
Gene Name: insulin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000207.2	440	UTR 3			NP_000198.1
NM_001185097.1	440	UTR 3			NP_001172026.1
NM_001185098.1	440	UTR 3			NP_001172027.1
NM_001291897.1	440	UTR 3			NP_001278826.1

Gene: INS-IGF2
Gene Name: INS-IGF2 readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001042376.2	440	Intron			NP_001035835.1

Gene: TH
Gene Name: tyrosine hydroxylase

There are no transcripts associated with this gene.

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