Variant #0000912922 (NC_000008.10:g.17815082T>G, NM_006197.3:c.1838T>G (PCM1))

Chromosome 8
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.17815082T>G
DNA change (hg38) -
Published as PCM1(NM_006197.3):c.1838T>G (p.I613S), PCM1(NM_006197.4):c.1838T>G (p.I613S)
ISCN -
DB-ID PCM1_000007 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) 0.0038 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCM1 NM_006197.3 -?/. - c.1838T>G r.(?) p.(Ile613Ser)


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