Product Details

SNP ID

rs1052371

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:7112582 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAGCTGTTCCTGAATATGTGCATGG[A/G]TGCACACTTATTTTGAGGCTCTTCC

Phenotype

MIM: 147670

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

INSR PubMed Links

Gene Details

Gene

INSR

Gene Name

insulin receptor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000208.3	9097	UTR 3			NP_000199.2
NM_001079817.2	9097	UTR 3			NP_001073285.1
XM_011527988.2	9097	UTR 3			XP_011526290.2
XM_011527989.2	9097	UTR 3			XP_011526291.2

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