Variant #0001011570 (NC_000009.11:g.98270588C>T, NM_000264.3:c.56G>A (PTCH1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.98270588C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID PTCH1_000772
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs587780708
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-10-11 12:42:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTCH1 NM_000264.3 ?/. - c.56G>A r.(?) p.(Gly19Asp)


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