Product Details

SNP ID

rs9683541

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:48990239 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTCACTTTCTTCCTCCATGAAAAC[A/C]CATCCCCTTGAGCAGAAGTAGATTT

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

CWH43 PubMed Links

Gene Details

Gene

CWH43

Gene Name

cell wall biogenesis 43 C-terminal homolog

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286791.1		Intron			NP_001273720.1
NM_025087.2		Intron			NP_079363.2
XM_011513755.1		Intron			XP_011512057.1
XM_011513756.2		Intron			XP_011512058.1
XM_011513757.2		Intron			XP_011512059.1
XM_011513758.1		Intron			XP_011512060.1
XM_011513759.1		Intron			XP_011512061.1

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