Product Details

SNP ID

rs145868278

Assay Type

Functionally tested

NCBI dbSNP Submissions

14

Location

Chr.1:15440369 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGAGTGGTGGGAGGAGAGGATGCCC[A/G]GCCCCACAGCTGGCCCTGGCAGGTA

Phenotype

MIM: 601405

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CTRC PubMed Links

Gene Details

Gene

CTRC

Gene Name

chymotrypsin C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007272.2	133	Missense Mutation	CAG,CGG	Q37R	NP_009203.2
XM_011540550.1	133	Missense Mutation	CAG,CGG	Q37R	XP_011538852.1

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