Product Details

SNP ID
rs34863121
Assay Type
Functionally tested
NCBI dbSNP Submissions
28
Location
Chr.1:109280836 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTGCTTGGTCTTGGAAGCCCTTTT[C/T]GAGTTGACAGAGAATCCGGAGGTAG
Phenotype
MIM: 604265 MIM: 613126
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CELSR2 PubMed Links

Gene Details

Gene
CELSR2
Gene Name
cadherin EGF LAG seven-pass G-type receptor 2
There are no transcripts associated with this gene.

Gene
PSRC1
Gene Name
proline and serine rich coiled-coil 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001005290.3 1074 Silent Mutation NP_001005290.1
NM_001032291.2 1074 Missense Mutation NP_001027462.1
NM_032636.7 1074 Missense Mutation NP_116025.1
XM_005271283.2 1074 Missense Mutation XP_005271340.1
XM_011542306.2 1074 Missense Mutation XP_011540608.1
XM_017002560.1 1074 Missense Mutation XP_016858049.1
XM_017002561.1 1074 Missense Mutation XP_016858050.1
XM_017002562.1 1074 Missense Mutation XP_016858051.1
XM_017002563.1 1074 Missense Mutation XP_016858052.1
XM_017002564.1 1074 Missense Mutation XP_016858053.1
XM_017002565.1 1074 Missense Mutation XP_016858054.1
XM_017002566.1 1074 Missense Mutation XP_016858055.1
XM_017002567.1 1074 Missense Mutation XP_016858056.1
XM_017002568.1 1074 Missense Mutation XP_016858057.1
XM_017002569.1 1074 Missense Mutation XP_016858058.1
XM_017002570.1 1074 Missense Mutation XP_016858059.1
XM_017002571.1 1074 Missense Mutation XP_016858060.1
XM_017002572.1 1074 Missense Mutation XP_016858061.1
XM_017002573.1 1074 Missense Mutation XP_016858062.1
XM_017002574.1 1074 Missense Mutation XP_016858063.1
XM_017002575.1 1074 Missense Mutation XP_016858064.1
XM_017002576.1 1074 Silent Mutation XP_016858065.1
XM_017002577.1 1074 Silent Mutation XP_016858066.1

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