Variant #0000248857 (NC_000008.10:g.17796382A>G, NM_006197.3:c.476= (PCM1))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.17796382A>G
DNA change (hg38) g.17938873A>G
Published as PCM1(NM_006197.4):c.476A>G (p.N159S), PCM1(NM_006197.4):c.476_478delACCinsGCC (p.N159S)
ISCN -
DB-ID PCM1_000003 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) 0.72191 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCM1 NM_006197.3 -/. - c.476= r.(=) p.(Ser159=)


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