Variant #0000803263 (NC_000007.13:g.82585303G>T, NM_033026.5:c.4966C>A (PCLO))

Chromosome 7
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.82585303G>T
DNA change (hg38) -
Published as PCLO(NM_033026.5):c.4966C>A (p.L1656I), PCLO(NM_033026.6):c.4966C>A (p.L1656I)
ISCN -
DB-ID PCLO_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) 8.0E-5 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 2021-09-17 14:40:49 +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     
PCLO NM_033026.5 -?/. - c.4966C>A r.(?) p.(Leu1656Ile)


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