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SNP ID

rs192163418

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:47090313 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCGAGGGACTCTGGATTGAAAACAA[C/G]AAGTGACAGAGCTTGTTGGAGGCAT

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

C2orf61 PubMed Links

Gene Details

Gene

C2orf61

Gene Name

chromosome 2 open reading frame 61

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001163561.1	708	Missense Mutation	TCT,TGT	S194C	NP_001157033.1
NM_173649.2	708	Intron			NP_775920.1

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