Product Details

SNP ID
rs17749087
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:93241563 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTGACTGCATCCACACTGTGGAAAT[C/G]TAACAGCTTTAGCCTGGGCACAGAA
Phenotype
MIM: 610386
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
BTBD7 PubMed Links

Gene Details

Gene
BTBD7
Gene Name
BTB domain containing 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001002860.3 3220 UTR 3 NP_001002860.2
NM_001289133.1 3220 UTR 3 NP_001276062.1
NM_018167.4 3220 Intron NP_060637.1
XM_011536939.2 3220 Intron XP_011535241.1
XM_017021438.1 3220 Intron XP_016876927.1

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