Product Details

SNP ID
rs141990944
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:141955007 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAGAATCCACAGTGAGCTCCTCCA[C/T]GGGGTTCCGCTCGGCGAAGGCAGCC
Phenotype
MIM: 605622 MIM: 605675
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PCDH12 PubMed Links

Gene Details

Gene
PCDH12
Gene Name
protocadherin 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_016580.3 4056 Missense Mutation NP_057664.1
Gene
RNF14
Gene Name
ring finger protein 14
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001201365.1 4056 Intron NP_001188294.1
NM_004290.4 4056 Intron NP_004281.1
NM_183398.2 4056 Intron NP_899645.1
NM_183399.2 4056 Intron NP_899646.1
NM_183400.2 4056 Intron NP_899647.1
NM_183401.2 4056 Intron NP_899648.1
XM_005268536.2 4056 Intron XP_005268593.1
XM_005268537.2 4056 Intron XP_005268594.1
XM_005268539.2 4056 Intron XP_005268596.1
XM_005268540.3 4056 Intron XP_005268597.1
XM_005268541.3 4056 Intron XP_005268598.1
XM_005268542.2 4056 Intron XP_005268599.1
XM_005268543.4 4056 Intron XP_005268600.1
XM_011537714.2 4056 Intron XP_011536016.1
XM_017010070.1 4056 Intron XP_016865559.1
XM_017010071.1 4056 Intron XP_016865560.1
XM_017010072.1 4056 Intron XP_016865561.1
XM_017010073.1 4056 Intron XP_016865562.1
XM_017010074.1 4056 Intron XP_016865563.1
XM_017010075.1 4056 Intron XP_016865564.1
XM_017010076.1 4056 Intron XP_016865565.1
XM_017010077.1 4056 Intron XP_016865566.1

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