Product Details

SNP ID

rs957998

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:170234990 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTTAAAATCAGATGGGTAAGAAGC[C/G]TGTTACTGATCATAAGCTAAATGTG

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

C5orf58 PubMed Links

Gene Details

Gene

C5orf58

Gene Name

chromosome 5 open reading frame 58

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001102609.2	189	Missense Mutation	CCT,CGT	P26R	NP_001096079.1
NM_001305393.1	189	Missense Mutation	CCT,CGT	P26R	NP_001292322.1
NM_001305394.1	189	Missense Mutation	CCT,CGT	P26R	NP_001292323.1
NM_001305395.1	189	Missense Mutation	CCT,CGT	P26R	NP_001292324.1
NM_001305396.1	189	Missense Mutation	CCT,CGT	P26R	NP_001292325.1
NM_001305397.1	189	Missense Mutation	CCT,CGT	P26R	NP_001292326.1
XM_011534432.2	189	Missense Mutation	CCT,CGT	P65R	XP_011532734.1
XM_017009029.1	189	Missense Mutation	CCT,CGT	P65R	XP_016864518.1
XM_017009030.1	189	Missense Mutation	CCT,CGT	P65R	XP_016864519.1
XM_017009031.1	189	Missense Mutation	CCT,CGT	P26R	XP_016864520.1
XM_017009032.1	189	Missense Mutation	CCT,CGT	P26R	XP_016864521.1
XM_017009033.1	189	Missense Mutation	CCT,CGT	P26R	XP_016864522.1

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