Product Details

SNP ID

rs11099642

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.4:75558301 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GAGTCTACAAAATAAATTGAGTTTT[G/T]CAGTTATTGTGAGTAAATCAATCAT

Phenotype

MIM: 614829

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

C4orf26 PubMed Links

Gene Details

Gene

C4orf26

Gene Name

chromosome 4 open reading frame 26

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001206981.1		Intron			NP_001193910.1
NM_001257072.1		Intron			NP_001244001.1
NM_178497.3		Intron			NP_848592.2
XM_011531668.2		Intron			XP_011529970.1

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