Variant #0000999312 (NC_000011.9:g.65978677C>T, NM_018026.3:c.607C>T (PACS1))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.65978677C>T
DNA change (hg38) -
Published as PACS1(NM_018026.3):c.607C>T (p.R203W, p.(Arg203Trp)), PACS1(NM_018026.4):c.607C>T (p.R203W)
ISCN -
DB-ID PACS1_000001 See all 19 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
PACS1 NM_018026.3 +/. - c.607C>T r.(?) p.(Arg203Trp)


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