Product Details

SNP ID

rs12859195

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:23344059 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCTAAAATACAGACTGATTCAAAG[A/G]GTCTGGGGTGGGAACTGCAAGTCTG

Phenotype

MIM: 300828

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

PTCHD1 PubMed Links

Gene Details

Gene

PTCHD1

Gene Name

patched domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173495.2		Intron			NP_775766.2
XM_011545449.2		Intron			XP_011543751.1

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