Product Details

SNP ID

rs150312431

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:9029355 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTCTTCTTCTTCCTCTTTCTGCTC[A/G]TCTGTGATGTATTCTTCAAGGACAT

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	1283	Silent Mutation	GAC,GAT	D115D	NP_995321.1
XM_011545464.2	1283	Silent Mutation	GAC,GAT	D115D	XP_011543766.1
XM_011545465.2	1283	Intron			XP_011543767.1

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