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SNP ID

rs145685617

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:132445697 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACGATTGCGGCGTTTCTCTACAGC[G/T]TGTCCATGGGCCCAGTGCCTGGCGT

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

C10orf91 PubMed Links

Gene Details

Gene

C10orf91

Gene Name

chromosome 10 open reading frame 91

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173541.2	71	Missense Mutation	GTG,TTG	V11L	NP_775812.1

Gene

LOC105378568

Gene Name

uncharacterized LOC105378568

There are no transcripts associated with this gene.

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