Product Details

SNP ID
rs10251388
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:51017193 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGTATGTGGTAAAAGTCTCAAAGGT[C/G]CAAAATCAGTCTAAGGCATGATTCT
Phenotype
MIM: 610317
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
COBL PubMed Links

Gene Details

Gene
COBL
Gene Name
cordon-bleu WH2 repeat protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001287436.1 4365 UTR 3 NP_001274365.1
NM_001287438.1 4365 Intron NP_001274367.1
NM_015198.3 4365 UTR 3 NP_056013.2
XM_005271750.1 4365 UTR 3 XP_005271807.1
XM_005271751.1 4365 UTR 3 XP_005271808.1
XM_005271756.1 4365 UTR 3 XP_005271813.1
XM_011515234.1 4365 UTR 3 XP_011513536.1
XM_011515235.1 4365 UTR 3 XP_011513537.1
XM_011515236.1 4365 UTR 3 XP_011513538.1
XM_011515237.1 4365 UTR 3 XP_011513539.1
XM_011515238.1 4365 UTR 3 XP_011513540.1
XM_011515239.1 4365 UTR 3 XP_011513541.1
XM_011515240.1 4365 UTR 3 XP_011513542.1
XM_011515241.1 4365 UTR 3 XP_011513543.1
XM_017011898.1 4365 UTR 3 XP_016867387.1
XM_017011899.1 4365 UTR 3 XP_016867388.1
XM_017011900.1 4365 UTR 3 XP_016867389.1
XM_017011901.1 4365 Intron XP_016867390.1

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