Product Details

SNP ID

rs142686945

Assay Type

Functionally tested

NCBI dbSNP Submissions

14

Location

Chr.1:107148796 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATCTGAAAGTGAAACTCGATCCTC[C/T]GGATATTACCTGTGGAGACCCTCCT

Phenotype

MIM: 608818

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NTNG1 PubMed Links

Gene Details

Gene

NTNG1

Gene Name

netrin G1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001113226.2	1963	Missense Mutation	CCG,CTG	P68L	NP_001106697.1
NM_001113228.2	1963	Missense Mutation	CCG,CTG	P68L	NP_001106699.1
NM_001312688.1	1963	Missense Mutation	CCG,CTG	P68L	NP_001299617.1
NM_014917.3	1963	Missense Mutation	CCG,CTG	P68L	NP_055732.2
XM_006710455.2	1963	Missense Mutation	CCG,CTG	P68L	XP_006710518.1
XM_006710456.3	1963	Missense Mutation	CCG,CTG	P68L	XP_006710519.1
XM_011541021.1	1963	Missense Mutation	CCG,CTG	P68L	XP_011539323.1
XM_011541024.2	1963	Missense Mutation	CCG,CTG	P68L	XP_011539326.1
XM_011541025.1	1963	Missense Mutation	CCG,CTG	P68L	XP_011539327.1
XM_017000680.1	1963	Missense Mutation	CCG,CTG	P68L	XP_016856169.1
XM_017000681.1	1963	Missense Mutation	CCG,CTG	P68L	XP_016856170.1
XM_017000682.1	1963	Missense Mutation	CCG,CTG	P68L	XP_016856171.1
XM_017000683.1	1963	Missense Mutation	CCG,CTG	P68L	XP_016856172.1
XM_017000684.1	1963	Missense Mutation	CCG,CTG	P68L	XP_016856173.1
XM_017000685.1	1963	Missense Mutation	CCG,CTG	P68L	XP_016856174.1
XM_017000686.1	1963	Missense Mutation	CCG,CTG	P68L	XP_016856175.1

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