Product Details

SNP ID

rs201746638

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:54906539 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCTTCCAGAGACTCTCCCAAAACC[A/G]TTCATCTGGGCCGAGCCCCATTTCA

Phenotype

MIM: 604530

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

NCR1 PubMed Links

Gene Details

Gene

NCR1

Gene Name

natural cytotoxicity triggering receptor 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145457.2	221	Silent Mutation	CCA,CCG	P29P	NP_001138929.2
NM_001145458.2	221	Silent Mutation	CCA,CCG	P29P	NP_001138930.2
NM_001242356.2	221	Intron			NP_001229285.1
NM_001242357.2	221	Intron			NP_001229286.1
NM_004829.6	221	Silent Mutation	CCA,CCG	P29P	NP_004820.2
XM_011527528.2	221	Silent Mutation	CCA,CCG	P29P	XP_011525830.1
XM_011527529.2	221	Silent Mutation	CCA,CCG	P29P	XP_011525831.1
XM_011527530.2	221	Silent Mutation	CCA,CCG	P29P	XP_011525832.1

View Full Product Details