Product Details

SNP ID

hCV27835943

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:107836935 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATAAGTTAAGGTAGGTTATTTTAGA[G/T]TACTAATGATTGGGTTTTTTTCTTT

Phenotype

MIM: 300204

Polymorphism

G/T, Transversion 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

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