Product Details

SNP ID
rs17137353
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:22843607 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGAAATGTCAAAAGTGCTGTGAAAA[G/A]TTTAAGGCTGTCTATGCACTTCATT
Phenotype
MIM: 608146
Polymorphism
G/A, Transition Substitution
Allele Nomenclature
Literature Links
NIPA2 PubMed Links

Gene Details

Gene
NIPA2
Gene Name
non imprinted in Prader-Willi/Angelman syndrome 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001008860.2 Intron NP_001008860.1
NM_001008892.2 Intron NP_001008892.1
NM_001008894.2 Intron NP_001008894.1
NM_001184888.1 Intron NP_001171817.1
NM_001184889.1 Intron NP_001171818.1
NM_030922.6 Intron NP_112184.4
XM_005272546.3 Intron XP_005272603.1
XM_005272547.4 Intron XP_005272604.1
XM_005272548.3 Intron XP_005272605.1
XM_005272550.3 Intron XP_005272607.1
XM_005272552.3 Intron XP_005272609.1
XM_005272553.4 Intron XP_005272610.1
XM_006720364.2 Intron XP_006720427.1
XM_006720365.2 Intron XP_006720428.1
XM_006720366.3 Intron XP_006720429.1
XM_006720367.1 Intron XP_006720430.1
XM_011543877.2 Intron XP_011542179.1
XM_011543878.2 Intron XP_011542180.1
XM_011543879.2 Intron XP_011542181.1
XM_011543880.2 Intron XP_011542182.1
XM_017022645.1 Intron XP_016878134.1
XM_017022646.1 Intron XP_016878135.1
XM_017022647.1 Intron XP_016878136.1
XM_017022648.1 Intron XP_016878137.1
XM_017022649.1 Intron XP_016878138.1
XM_017022650.1 Intron XP_016878139.1
XM_017022651.1 Intron XP_016878140.1
XM_017022652.1 Intron XP_016878141.1
XM_017022653.1 Intron XP_016878142.1
XM_017022654.1 Intron XP_016878143.1
XM_017022655.1 Intron XP_016878144.1
XM_017022656.1 Intron XP_016878145.1
XM_017022657.1 Intron XP_016878146.1
XM_017022658.1 Intron XP_016878147.1
XM_017022659.1 Intron XP_016878148.1
XM_017022660.1 Intron XP_016878149.1
XM_017022661.1 Intron XP_016878150.1
XM_017022662.1 Intron XP_016878151.1
XM_017022663.1 Intron XP_016878152.1

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