Product Details

SNP ID

rs201073413

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:9027885 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAACAGACCTTTACGAATTGGTCAC[A/G]TAGCAGCTTCATCTCTTTCAGCCTC

Phenotype

MIM: 300478

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM9B PubMed Links

Gene Details

Gene

FAM9B

Gene Name

family with sequence similarity 9 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_205849.3	1413	Missense Mutation	CGT,TGT	R159C	NP_995321.1
XM_011545464.2	1413	Missense Mutation	CGT,TGT	R159C	XP_011543766.1
XM_011545465.2	1413	Intron			XP_011543767.1

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