Variant #0000857510 (NC_000001.10:g.45295676A>G, NM_003738.4:c.840T>C (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.45295676A>G
DNA change (hg38) -
Published as PTCH2(NM_001166292.1):c.840T>C (p.S280=, p.(Ser280=)), PTCH2(NM_001166292.2):c.840T>C (p.S280=), PTCH2(NM_003738.5):c.840T>C (p.S280=)
ISCN -
DB-ID PTCH2_000023 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) 0.0054 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 2022-05-09 15:51:19 +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.840T>C r.(?) p.(Ser280=)


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