Product Details

SNP ID

rs200888528

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:99513208 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCCAGAAGAGTCTGCCACATCAAA[A/G]GTAAGGTGACTTAAGGTCCTAGTAT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C4orf17 PubMed Links

Gene Details

Gene

C4orf17

Gene Name

chromosome 4 open reading frame 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032149.2	489	Missense Mutation	AGC,GGC	S43G	NP_115525.2
XM_011532315.1	489	Missense Mutation	AGC,GGC	S43G	XP_011530617.1

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