Product Details

SNP ID

rs148958066

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:132166858 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTGCATCTGCTGGCGCTCTTCCT[A/G]CACTGCCTCCCTCTGGCCTCTGGGG

Phenotype

Polymorphism

A/G, 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	824	Silent Mutation	CTA,CTG	L9L	NP_115925.2
XM_006717304.3	824	Silent Mutation	CTA,CTG	L9L	XP_006717367.1
XM_011519094.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517396.1
XM_011519096.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517398.1
XM_011519097.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517399.1
XM_011519098.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517400.1
XM_011519099.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517401.1
XM_011519100.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517402.1
XM_011519102.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517404.1
XM_011519103.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517405.1
XM_011519104.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517406.1
XM_011519105.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517407.1
XM_011519106.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517408.1
XM_011519107.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517409.1
XM_011519108.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517410.1
XM_011519109.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517411.1
XM_011519110.2	824	Silent Mutation	CTA,CTG	L9L	XP_011517412.1
XM_011519112.2	824	Intron			XP_011517414.1
XM_011519113.2	824	Intron			XP_011517415.1
XM_017015212.1	824	Silent Mutation	CTA,CTG	L9L	XP_016870701.1
XM_017015213.1	824	Silent Mutation	CTA,CTG	L9L	XP_016870702.1
XM_017015214.1	824	Silent Mutation	CTA,CTG	L9L	XP_016870703.1
XM_017015215.1	824	Intron			XP_016870704.1
XM_017015216.1	824	Silent Mutation	CTA,CTG	L9L	XP_016870705.1

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