Product Details

SNP ID

rs9294867

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:70415513 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CATCAAACCACACTTCTTTGAGAAG[A/G]ACTAGCAATTGTGTATGGTAAGAGG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM135A PubMed Links

Gene Details

Gene

FAM135A

Gene Name

family with sequence similarity 135 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001105531.2		Intron			NP_001099001.1
NM_001162529.1		Intron			NP_001156001.1
NM_020819.4		Intron			NP_065870.3
XM_005248743.1		Intron			XP_005248800.1
XM_005248744.4		Intron			XP_005248801.1
XM_005248745.2		Intron			XP_005248802.1
XM_005248748.2		Intron			XP_005248805.1
XM_005248749.1		Intron			XP_005248806.1
XM_005248751.2		Intron			XP_005248808.1
XM_011535993.2		Intron			XP_011534295.1
XM_011535994.2		Intron			XP_011534296.1
XM_011535995.2		Intron			XP_011534297.1
XM_011535996.2		Intron			XP_011534298.1
XM_011535997.2		Intron			XP_011534299.1
XM_017011124.1		Intron			XP_016866613.1
XM_017011125.1		Intron			XP_016866614.1
XM_017011126.1		Intron			XP_016866615.1
XM_017011127.1		Intron			XP_016866616.1
XM_017011128.1		Intron			XP_016866617.1
XM_017011129.1		Intron			XP_016866618.1
XM_017011130.1		Intron			XP_016866619.1
XM_017011131.1		Intron			XP_016866620.1
XM_017011132.1		Intron			XP_016866621.1
XM_017011133.1		Intron			XP_016866622.1
XM_017011134.1		Intron			XP_016866623.1
XM_017011135.1		Intron			XP_016866624.1
XM_017011136.1		Intron			XP_016866625.1

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