Product Details

SNP ID

rs140992561

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:66798209 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCTGGATTTTCCTCAGAAAACTCA[C/T]GTTTATGTGGGAGCTGGAAGGAGTT

Phenotype

MIM: 606413

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

INSL5 PubMed Links

Gene Details

Gene

INSL5

Gene Name

insulin like 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005478.4	250	Missense Mutation	CAT,CGT	H71R	NP_005469.2

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