Product Details

SNP ID

rs11727634

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:37462152 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAAACATTTAAATTCCAAATCTGTA[C/T]GTCCATGTAAATAGTGGGGAAATTT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

C4orf19 PubMed Links

Gene Details

Gene

C4orf19

Gene Name

chromosome 4 open reading frame 19

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001104629.1		Intron			NP_001098099.1
NM_018302.2		Intron			NP_060772.2
XM_011513712.2		Intron			XP_011512014.1
XM_011513713.2		Intron			XP_011512015.1
XM_017008361.1		Intron			XP_016863850.1

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