Product Details

SNP ID

rs150562029

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:153594638 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATGCTGTCCCGGAGTTCCCAGAAG[C/T]GGGAGTCCAATTCCAGGGGCTCACC

Phenotype

MIM: 300708

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM58A PubMed Links

Gene Details

Gene

FAM58A

Gene Name

family with sequence similarity 58 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130997.2	966	Intron			NP_001124469.1
NM_152274.4	966	Intron			NP_689487.2
XM_005277920.4	966	Intron			XP_005277977.1
XM_005277921.4	966	Intron			XP_005277978.1
XM_011531214.2	966	Missense Mutation	CAC,CGC	H71R	XP_011529516.1
XM_011531215.2	966	Missense Mutation	CAC,CGC	H71R	XP_011529517.1

Gene

LOC105373383

Gene Name

uncharacterized LOC105373383

There are no transcripts associated with this gene.

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