Product Details

SNP ID

rs138339976

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:54906676 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTGCCGTGGACAGACCAAAACCCC[C/G]TGAGCGGATTAACAAAGTCCAATTC

Phenotype

MIM: 604530

Polymorphism

C/G, Transversion 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	358	Missense Mutation	CCT,CGT	P75R	NP_001138929.2
NM_001145458.2	358	Missense Mutation	CCT,CGT	P75R	NP_001138930.2
NM_001242356.2	358	Intron			NP_001229285.1
NM_001242357.2	358	Intron			NP_001229286.1
NM_004829.6	358	Missense Mutation	CCT,CGT	P75R	NP_004820.2
XM_011527528.2	358	Missense Mutation	CCT,CGT	P75R	XP_011525830.1
XM_011527529.2	358	Missense Mutation	CCT,CGT	P75R	XP_011525831.1
XM_011527530.2	358	Missense Mutation	CCT,CGT	P75R	XP_011525832.1

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