Genomic variant #0000043662

Individual ID 00022096
Chromosome 9
Allele Parent #2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.98244242T>C
Reference -
DB-ID PTCH1_000133 See all 7 reported entries
dbSNP ID rs1805154
Variant remarks -
Genetic origin -
Segregation -
Also Known As -
Is Greek Founder -
Geographic Origin (for founder variants) -
Average frequency (large NGS studies) Retrieve
Average frequency in greek population 0.00119
Allele Count 7
Allele Number 5900
Owner Stevi Xera
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTCH1 NM_000264.3 ./. - c.735A>G r.(=) p.(=)
PTCH1 NM_001083602.1 ./. - c.537A>G r.(=) p.(=)
PTCH1 NM_001083603.1 ./. - c.732A>G r.(=) p.(=)
PTCH1 NM_001083604.1 ./. - c.282A>G r.(=) p.(=)
PTCH1 NM_001083605.1 ./. - c.282A>G r.(=) p.(=)
PTCH1 NM_001083606.1 ./. - c.282A>G r.(=) p.(=)
PTCH1 NM_001083607.1 ./. - c.282A>G r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000007594 DNA SEQ-NG-I 1 - 37 Stevi Xera