Variant #0000675871 (NC_000001.10:g.45293709G>T, NM_003738.4:c.1864C>A (PTCH2))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45293709G>T
DNA change (hg38) -
Published as PTCH2(NM_001166292.1):c.1864C>A (p.(His622Asn)), PTCH2(NM_003738.5):c.1864C>A (p.H622N)
ISCN -
DB-ID PTCH2_000014 See all 3 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) 0.00225 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTCH2 NM_003738.4 -/. - c.1864C>A r.(?) p.(His622Asn)


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