Product Details

SNP ID

rs202103984

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:43362250 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAGGTGGGGCTGAGGGCCTGGAGT[C/G]TCTCACTTGGGGGGTGGGGCTGGCA

Phenotype

MIM: 162860

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CD177 PubMed Links

Gene Details

Gene

CD177

Gene Name

CD177 molecule

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020406.3	1300	Missense Mutation	TCT,TGT	S415C	NP_065139.2
XM_017027021.1	1300	Intron			XP_016882510.1
XM_017027022.1	1300	Intron			XP_016882511.1

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