Variant #0000012692 (NC_000009.11:-, PTCH1(NM_000264.3):c.?)

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID PTCH1_00003 See all 5 reported entries
Frequency -
Variant remarks 1439-39G>C
ClassClinical -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTCH1 NM_000264.3 ./. 11 c.? - -