Product Details

SNP ID

rs139429864

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:6211703 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTTGGCGTTCAGGGGCCCCGCCCC[A/G]GGTGAGTAGAACTGGAGTTGAAGCC

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	3059	Intron			NP_775796.2
XM_011519926.2	3059	Intron			XP_011518228.1
XM_011519927.2	3059	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	3059	Silent Mutation			NP_001092264.1
NM_032127.3	3059	Silent Mutation			NP_115503.2
XM_006718343.2	3059	Missense Mutation			XP_006718406.1
XM_011520397.2	3059	Missense Mutation			XP_011518699.1
XM_011520398.2	3059	Intron			XP_011518700.1
XM_011520399.2	3059	Intron			XP_011518701.1

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