Product Details

SNP ID
rs73568438
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:111779264 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AACCAAAAACGCACGCCCTTCTCAT[G/T]TGGCAACTTGCAATTCCCGAGTTAA
Phenotype
MIM: 606941
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
ALG9 PubMed Links

Gene Details

Gene
ALG9
Gene Name
ALG9, alpha-1,2-mannosyltransferase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001077690.1 Intron NP_001071158.1
NM_001077691.1 Intron NP_001071159.1
NM_001077692.1 Intron NP_001071160.1
NM_024740.2 Intron NP_079016.2
XM_005277723.4 Intron XP_005277780.1
XM_005277724.4 Intron XP_005277781.1
XM_006718913.2 Intron XP_006718976.1
XM_011542992.1 Intron XP_011541294.1
XM_017018313.1 Intron XP_016873802.1
XM_017018314.1 Intron XP_016873803.1
XM_017018315.1 Intron XP_016873804.1
XM_017018316.1 Intron XP_016873805.1
XM_017018317.1 Intron XP_016873806.1
XM_017018318.1 Intron XP_016873807.1
XM_017018319.1 Intron XP_016873808.1
XM_017018320.1 Intron XP_016873809.1
XM_017018321.1 Intron XP_016873810.1
XM_017018322.1 Intron XP_016873811.1
XM_017018323.1 Intron XP_016873812.1
XM_017018324.1 Intron XP_016873813.1
XM_017018325.1 Intron XP_016873814.1
XM_017018326.1 Intron XP_016873815.1

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