Product Details

SNP ID
rs7028698
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:126339239 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TAGAAGGCTGCAGTCATTTTTAATG[A/G]CCTCTGCCTTTTCTGATTCTAGGCT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MVB12B PubMed Links

Gene Details

Gene
MVB12B
Gene Name
multivesicular body subunit 12B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001011703.2 Intron NP_001011703.1
NM_033446.2 Intron NP_258257.1
XM_005252297.1 Intron XP_005252354.1
XM_017015275.1 Intron XP_016870764.1
XM_017015276.1 Intron XP_016870765.1
XM_017015277.1 Intron XP_016870766.1
XM_017015278.1 Intron XP_016870767.1
XM_017015279.1 Intron XP_016870768.1

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