Product Details

SNP ID

rs184977421

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:15440362 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCCGCCCGAGTGGTGGGAGGAGAG[A/G]ATGCCCGGCCCCACAGCTGGCCCTG

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	126	Missense Mutation	AAT,GAT	N35D	NP_009203.2
XM_011540550.1	126	Missense Mutation	AAT,GAT	N35D	XP_011538852.1

View Full Product Details