Variant #0000608339 (NC_000003.11:g.135969363G>C, NM_000532.4:c.146G>C (PCCB))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.135969363G>C
DNA change (hg38) g.136250521G>C
Published as PCCB(NM_000532.4):c.146G>C (p.(Gly49Ala))
ISCN -
DB-ID STAG1_000022
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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.146G>C r.(?) p.(Gly49Ala)
STAG1 NM_005862.2 ?/. - c.*87733C>G r.(=) p.(=)


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