Product Details

SNP ID
rs34702192
Assay Type
Functionally tested
NCBI dbSNP Submissions
15
Location
Chr.1:37475795 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCGAGCGGGAGCGCCAGACCTCAC[C/T]GGACCCCTGCCCTCAGCTCCCTCTA
Phenotype
MIM: 610562
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LINC01137 PubMed Links

Gene Details

Gene
LINC01137
Gene Name
long intergenic non-protein coding RNA 1137
There are no transcripts associated with this gene.

Gene
MIR6732
Gene Name
microRNA 6732
There are no transcripts associated with this gene.

Gene
ZC3H12A
Gene Name
zinc finger CCCH-type containing 12A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001323550.1 449 Missense Mutation CCG,CTG P100L NP_001310479.1
NM_001323551.1 449 UTR 5 NP_001310480.1
NM_025079.2 449 Missense Mutation CCG,CTG P100L NP_079355.2
XM_011542198.2 449 Missense Mutation CCG,CTG P100L XP_011540500.1

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