Product Details

SNP ID
rs151183349
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:156643021 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTCATAAAATACACCATGTCCAA[A/G]ATCTAAAAGGGCCAATTCCAAATTA
Phenotype
MIM: 610242 MIM: 610241
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C7orf13 PubMed Links

Gene Details

Gene
C7orf13
Gene Name
chromosome 7 open reading frame 13
There are no transcripts associated with this gene.

Gene
RNF32
Gene Name
ring finger protein 32
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001184996.1 109 Intron NP_001171925.1
NM_001184997.1 109 UTR 5 NP_001171926.1
NM_001308273.1 109 Intron NP_001295202.1
NM_001308274.1 109 Intron NP_001295203.1
NM_030936.3 109 Intron NP_112198.1
XM_005249522.4 109 Intron XP_005249579.1
XM_011515804.2 109 UTR 5 XP_011514106.1
XM_011515805.2 109 UTR 5 XP_011514107.1
XM_011515806.2 109 Intron XP_011514108.1
XM_011515807.2 109 Intron XP_011514109.1
XM_011515808.2 109 Intron XP_011514110.1
XM_011515809.2 109 Intron XP_011514111.1
XM_011515810.2 109 Intron XP_011514112.1
XM_011515811.2 109 Intron XP_011514113.1
XM_011515812.2 109 Intron XP_011514114.1
XM_011515813.2 109 Intron XP_011514115.1
XM_017011753.1 109 Intron XP_016867242.1
XM_017011754.1 109 Intron XP_016867243.1
XM_017011755.1 109 Intron XP_016867244.1

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