Product Details

SNP ID
rs6668194
Assay Type
Functionally tested
NCBI dbSNP Submissions
13
Location
Chr.1:173933384 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACCTATTAGGAATAGATTTATTATT[A/T]AAAGGTGTTACTTATTCCTGGTGGT
Phenotype
MIM: 609424
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
RC3H1 PubMed Links

Gene Details

Gene
RC3H1
Gene Name
ring finger and CCCH-type domains 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001300850.1 8829 UTR 3 NP_001287779.1
NM_001300851.1 8829 UTR 3 NP_001287780.1
NM_001300852.1 8829 UTR 3 NP_001287781.1
NM_172071.3 8829 UTR 3 NP_742068.1
XM_005244921.3 8829 UTR 3 XP_005244978.1
XM_011509231.2 8829 UTR 3 XP_011507533.1

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