Product Details

SNP ID

rs137862169

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:132167039 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGAGACCCCCCTGAGAGGTTCTGC[G/T]CCCATGTAAGTCCACTTACTGCTCT

Phenotype

Polymorphism

G/T, Transversion 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	1005	Missense Mutation	GCC,TCC	A70S	NP_115925.2
XM_006717304.3	1005	Missense Mutation	GCC,TCC	A70S	XP_006717367.1
XM_011519094.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517396.1
XM_011519096.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517398.1
XM_011519097.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517399.1
XM_011519098.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517400.1
XM_011519099.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517401.1
XM_011519100.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517402.1
XM_011519102.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517404.1
XM_011519103.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517405.1
XM_011519104.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517406.1
XM_011519105.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517407.1
XM_011519106.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517408.1
XM_011519107.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517409.1
XM_011519108.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517410.1
XM_011519109.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517411.1
XM_011519110.2	1005	Missense Mutation	GCC,TCC	A70S	XP_011517412.1
XM_011519112.2	1005	Intron			XP_011517414.1
XM_011519113.2	1005	Intron			XP_011517415.1
XM_017015212.1	1005	Missense Mutation	GCC,TCC	A70S	XP_016870701.1
XM_017015213.1	1005	Missense Mutation	GCC,TCC	A70S	XP_016870702.1
XM_017015214.1	1005	Missense Mutation	GCC,TCC	A70S	XP_016870703.1
XM_017015215.1	1005	Intron			XP_016870704.1
XM_017015216.1	1005	Missense Mutation	GCC,TCC	A70S	XP_016870705.1

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