Product Details

SNP ID
rs7597440
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:200977287 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCACTGCCTCCCCAAACCCATGGGA[A/G]ACTGGGTTTGATTCTGGCTCTGCTT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FAM126B PubMed Links

Gene Details

Gene
FAM126B
Gene Name
family with sequence similarity 126 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321618.1 5822 UTR 3 NP_001308547.1
NM_001321619.1 5822 UTR 3 NP_001308548.1
NM_001321621.1 5822 UTR 3 NP_001308550.1
NM_001321622.1 5822 UTR 3 NP_001308551.1
NM_001321623.1 5822 UTR 3 NP_001308552.1
NM_001321624.1 5822 UTR 3 NP_001308553.1
NM_001321625.1 5822 UTR 3 NP_001308554.1
NM_001321626.1 5822 UTR 3 NP_001308555.1
NM_001321627.1 5822 UTR 3 NP_001308556.1
NM_001321628.1 5822 UTR 3 NP_001308557.1
NM_001321629.1 5822 UTR 3 NP_001308558.1
NM_173822.4 5822 UTR 3 NP_776183.1
XM_006712443.3 5822 Intron XP_006712506.1
XM_011511002.2 5822 Intron XP_011509304.1
XM_017003879.1 5822 Intron XP_016859368.1
XM_017003880.1 5822 Intron XP_016859369.1
XM_017003881.1 5822 Intron XP_016859370.1
XM_017003882.1 5822 Intron XP_016859371.1
XM_017003883.1 5822 Intron XP_016859372.1

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