Product Details

SNP ID
rs200408330
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.13:66304725 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTATAAGACTTCAGATTTGCCAGA[C/G]GAATGTCTGTCATGTGGCTGCCATT
Phenotype
MIM: 603581
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
PCDH9 PubMed Links

Gene Details

Gene
PCDH9
Gene Name
protocadherin 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318372.1 4336 Missense Mutation CCT,CGT P1173R NP_001305301.1
NM_001318373.1 4336 Missense Mutation CCT,CGT P1139R NP_001305302.1
NM_001318374.1 4336 Intron NP_001305303.1
NM_020403.4 4336 Missense Mutation CCT,CGT P1181R NP_065136.1
NM_203487.2 4336 Missense Mutation CCT,CGT P1215R NP_982354.1
XM_005266408.3 4336 Intron XP_005266465.1
XM_011535099.2 4336 Intron XP_011533401.1
XM_017020619.1 4336 Missense Mutation CCT,CGT P1215R XP_016876108.1
XM_017020620.1 4336 Intron XP_016876109.1
XM_017020621.1 4336 Intron XP_016876110.1

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