Variant #0000815928 (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 -
ISCN -
DB-ID PACS1_000001 See all 19 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs398123009
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 2021-10-26 08:02:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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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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