Variant #0000538757 (NC_000009.11:g.98231110G>A, NM_000264.3:c.2173C>T (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.98231110G>A
DNA change (hg38) g.95468828G>A
Published as LOC100507346(NR_038982.1):n.766G>A (-), PTCH1(NM_000264.5):c.2173C>T (p.P725S), PTCH1(NM_001083602.1):c.1975C>T (p.P659S)
ISCN -
DB-ID PTCH1_000473 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0009 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTCH1 NM_000264.3 ?/. - c.2173C>T r.(?) p.(Pro725Ser)


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