Variant #0000518056 (NC_000003.11:g.136047691C>T, NM_000532.4:c.1490C>T (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.136047691C>T
DNA change (hg38) g.136328849C>T
Published as PCCB(NM_000532.5):c.1490C>T (p.A497V), PCCB(NM_001178014.1):c.1550C>T (p.A517V), PCCB(NM_001178014.2):c.1550C>T (p.A517V)
ISCN -
DB-ID PCCB_000020 See all 11 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) 0.00204 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 2019-07-18 18:22:55 +02:00 (CEST)
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.1490C>T r.(?) p.(Ala497Val)
STAG1 NM_005862.2 -?/. - c.*9405G>A r.(=) p.(=)


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