Product Details

SNP ID

rs180953673

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:126256817 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCGATCTTCCAGAATATTTCAAGC[A/G]ACTGACATGTGAGATCTCCACAAGG

Phenotype

MIM: 616587 MIM: 182180

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM118B PubMed Links

Gene Details

Gene

FAM118B

Gene Name

family with sequence similarity 118 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024556.3	2061	Missense Mutation	CAA,CGA	Q316R	NP_078832.1
XM_005271665.3	2061	Missense Mutation	CAA,CGA	Q316R	XP_005271722.1
XM_011542977.2	2061	Missense Mutation	CAA,CGA	Q316R	XP_011541279.1
XM_011542978.2	2061	Missense Mutation	CAA,CGA	Q161R	XP_011541280.1
XM_017018285.1	2061	Missense Mutation	CAA,CGA	Q316R	XP_016873774.1
XM_017018286.1	2061	Missense Mutation	CAA,CGA	Q161R	XP_016873775.1

Gene

SRPRA

Gene Name

SRP receptor alpha subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001177842.1	2061	Intron			NP_001171313.1
NM_003139.3	2061	Intron			NP_003130.2
XM_017018179.1	2061	UTR 3			XP_016873668.1

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