Product Details

SNP ID

rs2797199

Assay Type

Functionally tested

NCBI dbSNP Submissions

44

Location

Chr.1:115830286 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCTCACTCCAAAGTTCCCTCCTGA[C/G]TTTAGTGCCTGGCCAATGGCTGAAA

Phenotype

MIM: 162361

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

NHLH2 PubMed Links

Gene Details

Gene

NHLH2

Gene Name

nescient helix-loop-helix 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001111061.1		Intron			NP_001104531.1
NM_005599.3		Intron			NP_005590.1
XM_017001370.1		Intron			XP_016856859.1

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