Product Details

SNP ID

rs146871349

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:6211702 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCTTGGCGTTCAGGGGCCCCGCCC[C/T]GGGTGAGTAGAACTGGAGTTGAAGC

Phenotype

Polymorphism

C/T, 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	3060	Intron			NP_775796.2
XM_011519926.2	3060	Intron			XP_011518228.1
XM_011519927.2	3060	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	3060	Missense Mutation	CAG,CGG	Q908R	NP_001092264.1
NM_032127.3	3060	Missense Mutation	CAG,CGG	Q922R	NP_115503.2
XM_006718343.2	3060	Missense Mutation	CAG,CGG	Q922R	XP_006718406.1
XM_011520397.2	3060	Missense Mutation	CAG,CGG	Q922R	XP_011518699.1
XM_011520398.2	3060	Intron			XP_011518700.1
XM_011520399.2	3060	Intron			XP_011518701.1

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