Product Details

SNP ID

rs116637423

Assay Type

Functionally Tested

NCBI dbSNP Submissions

7

Location

Chr.1:107144946 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTGAAGAGGTAGAACTGGAGCTGC[C/T]CAGAGCTCTTATGAATCTGTTCTTA

Phenotype

MIM: 608818

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NTNG1 PubMed Links

Additional Information

For this assay, SNP(s) [rs76335573] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

NTNG1

Gene Name

netrin G1

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

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