Product Details

SNP ID
rs10901132
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:132164706 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCCAGGCAGGCTCTGTAACAGGT[C/T]CCCCTTTAAACAGCCAGAGGTGAGA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
NTNG2 PubMed Links

Gene Details

Gene
NTNG2
Gene Name
netrin G2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032536.2 Intron NP_115925.2
XM_006717304.3 Intron XP_006717367.1
XM_011519094.2 Intron XP_011517396.1
XM_011519096.2 Intron XP_011517398.1
XM_011519097.2 Intron XP_011517399.1
XM_011519098.2 Intron XP_011517400.1
XM_011519099.2 Intron XP_011517401.1
XM_011519100.2 Intron XP_011517402.1
XM_011519102.2 Intron XP_011517404.1
XM_011519103.2 Intron XP_011517405.1
XM_011519104.2 Intron XP_011517406.1
XM_011519105.2 Intron XP_011517407.1
XM_011519106.2 Intron XP_011517408.1
XM_011519107.2 Intron XP_011517409.1
XM_011519108.2 Intron XP_011517410.1
XM_011519109.2 Intron XP_011517411.1
XM_011519110.2 Intron XP_011517412.1
XM_011519112.2 Intron XP_011517414.1
XM_011519113.2 Intron XP_011517415.1
XM_017015212.1 Intron XP_016870701.1
XM_017015213.1 Intron XP_016870702.1
XM_017015214.1 Intron XP_016870703.1
XM_017015215.1 Intron XP_016870704.1
XM_017015216.1 Intron XP_016870705.1

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