Product Details

SNP ID

rs7879230

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:107829243 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGTTAGTGGATTGACTGGGTGTAAG[C/T]AGGAATCTTAGCTTACTGAAAACCT

Phenotype

MIM: 300204

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MID2 PubMed Links

Gene Details

Gene

MID2

Gene Name

midline 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012216.3		Intron			NP_036348.2
NM_052817.2		Intron			NP_438112.2
XM_005262062.4		Intron			XP_005262119.1
XM_017029239.1		Intron			XP_016884728.1

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