Product Details

SNP ID
rs144662522
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:74900240 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCCTAAACAACTGACCATTTCTAC[C/T]CTGCCTCACTGCACTGTCCCACCAG
Phenotype
MIM: 154550
Polymorphism
C/T, 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 3067 UTR 3 NP_001308849.1
NM_001321921.1 3067 Intron NP_001308850.1
NM_001321922.1 3067 UTR 3 NP_001308851.1
NM_001321923.1 3067 UTR 3 NP_001308852.1
NM_020447.4 3067 UTR 3 NP_065180.1
XM_017022433.1 3067 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 3067 Intron NP_001276084.1
NM_001289156.1 3067 Intron NP_001276085.1
NM_001289157.1 3067 Intron NP_001276086.1
NM_002435.2 3067 Intron NP_002426.1
XM_011521592.1 3067 Intron XP_011519894.1
XM_011521593.2 3067 Intron XP_011519895.1
XM_017022207.1 3067 Intron XP_016877696.1
XM_017022208.1 3067 Intron XP_016877697.1
XM_017022209.1 3067 Intron XP_016877698.1

View Full Product Details