Variant #0000858812 (NC_000003.11:g.135969299C>G, NM_000532.4:c.82C>G (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.135969299C>G
DNA change (hg38) -
Published as PCCB(NM_000532.5):c.82C>G (p.L28V), PCCB(NM_001178014.1):c.82C>G (p.L28V)
ISCN -
DB-ID STAG1_000040 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) 0.00023 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +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     
PCCB NM_000532.4 -?/. - c.82C>G r.(?) p.(Leu28Val)
STAG1 NM_005862.2 -?/. - c.*87797G>C r.(=) p.(=)


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