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SNP ID

rs61732571

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:8791301 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTACAGTTCTGACACGATTCTTTTT[A/G]AAAACACGGCTAGTTATCAAGTTCA

Phenotype

MIM: 300477

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM9A PubMed Links

Gene Details

Gene

FAM9A

Gene Name

family with sequence similarity 9 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001171186.1		Intron			NP_001164657.1
NM_174951.3		Intron			NP_777611.1

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