Product Details

SNP ID

rs6517376

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.21:36703581 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCTTTCTGGGTGACCACCTTTTCT[C/T]CCCTTTGACAGTGAACTAATACATT

Phenotype

MIM: 600892

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SIM2 PubMed Links

Gene Details

Gene

SIM2

Gene Name

single-minded family bHLH transcription factor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005069.4		Intron			NP_005060.1
NM_009586.3		Intron			NP_033664.2
XM_011529694.1		Intron			XP_011527996.1
XM_017028442.1		Intron			XP_016883931.1

View Full Product Details