Variant #0000885568 (NC_000003.11:g.136002681G>A, NM_000532.4:c.546G>A (PCCB))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.136002681G>A
DNA change (hg38) -
Published as PCCB(NM_000532.5):c.546G>A (p.R182=), PCCB(NM_001178014.2):c.606G>A (p.R202=)
ISCN -
DB-ID STAG1_000013 See all 2 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) 0.00122 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCCB NM_000532.4 -?/. - c.546G>A r.(?) p.(Arg182=)
STAG1 NM_005862.2 -?/. - c.*54415C>T r.(=) p.(=)


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