Product Details

SNP ID
rs12192111
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:127269684 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAGCAGGAGATGATGAGGGCTAAAA[A/G]TTGAGACATTAGGGCATTTAGTTAC
Phenotype
MIM: 612137
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RNF146 PubMed Links

Gene Details

Gene
RNF146
Gene Name
ring finger protein 146
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001242844.1 Intron NP_001229773.1
NM_001242845.1 Intron NP_001229774.1
NM_001242846.1 Intron NP_001229775.1
NM_001242847.1 Intron NP_001229776.1
NM_001242848.1 Intron NP_001229777.1
NM_001242849.1 Intron NP_001229778.1
NM_001242850.1 Intron NP_001229779.1
NM_001242851.1 Intron NP_001229780.1
NM_001242852.1 Intron NP_001229781.1
NM_030963.3 Intron NP_112225.2
XM_006715571.3 Intron XP_006715634.1
XM_011536161.2 Intron XP_011534463.1
XM_011536162.2 Intron XP_011534464.1
XM_011536163.2 Intron XP_011534465.1
XM_011536164.2 Intron XP_011534466.1
XM_017011336.1 Intron XP_016866825.1
XM_017011337.1 Intron XP_016866826.1
XM_017011338.1 Intron XP_016866827.1
XM_017011339.1 Intron XP_016866828.1
XM_017011340.1 Intron XP_016866829.1
XM_017011341.1 Intron XP_016866830.1
XM_017011342.1 Intron XP_016866831.1
XM_017011343.1 Intron XP_016866832.1

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