Product Details

SNP ID
rs7497201
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:74898349 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCTATTTCATACAGCTTCTCGGGGG[A/G]GTGAGCAGGCTACACTCCAGAACAC
Phenotype
MIM: 154550
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
FAM219B PubMed Links

Gene Details

Gene
FAM219B
Gene Name
family with sequence similarity 219 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321920.1 1826 Intron NP_001308849.1
NM_001321921.1 1826 Intron NP_001308850.1
NM_001321922.1 1826 Intron NP_001308851.1
NM_001321923.1 1826 Intron NP_001308852.1
NM_020447.4 1826 Intron NP_065180.1
XM_017022433.1 1826 Intron XP_016877922.1
Gene
MPI
Gene Name
mannose phosphate isomerase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001289155.1 1826 UTR 3 NP_001276084.1
NM_001289156.1 1826 UTR 3 NP_001276085.1
NM_001289157.1 1826 UTR 3 NP_001276086.1
NM_002435.2 1826 UTR 3 NP_002426.1
XM_011521592.1 1826 Intron XP_011519894.1
XM_011521593.2 1826 UTR 3 XP_011519895.1
XM_017022207.1 1826 Intron XP_016877696.1
XM_017022208.1 1826 Intron XP_016877697.1
XM_017022209.1 1826 Intron XP_016877698.1

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