Product Details

SNP ID
hCV15900022
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:91803991 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTCCCACATTTTTTCAATCACATA[G/T]GGATAGAGATAATCCCCACTGTTGG
Phenotype
MIM: 300246
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
PCDH11X PubMed Links

Gene Details

Gene
PCDH11X
Gene Name
protocadherin 11 X-linked
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001168360.1 Intron NP_001161832.1
NM_001168361.1 Intron NP_001161833.1
NM_001168362.1 Intron NP_001161834.1
NM_001168363.1 Intron NP_001161835.1
NM_032968.4 Intron NP_116750.1
NM_032969.4 Intron NP_116751.1

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