Product Details

SNP ID

rs200174554

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:6211667 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCACAGTAGACAGCATTCTTGACTC[A/G]AAGAGCCTCACCTTGGCGTTCAGGG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C11orf42 PubMed Links

Gene Details

Gene

C11orf42

Gene Name

chromosome 11 open reading frame 42

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173525.2	3095	Intron			NP_775796.2
XM_011519926.2	3095	Intron			XP_011518228.1
XM_011519927.2	3095	Intron			XP_011518229.1

Gene

FAM160A2

Gene Name

family with sequence similarity 160 member A2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001098794.1	3095	Nonsense Mutation	CGA,TGA	R920*	NP_001092264.1
NM_032127.3	3095	Nonsense Mutation	CGA,TGA	R934*	NP_115503.2
XM_006718343.2	3095	Nonsense Mutation	CGA,TGA	R934*	XP_006718406.1
XM_011520397.2	3095	Nonsense Mutation	CGA,TGA	R934*	XP_011518699.1
XM_011520398.2	3095	Intron			XP_011518700.1
XM_011520399.2	3095	Intron			XP_011518701.1

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