Variant #0000990553 (NC_000001.10:g.172411298del, NM_153747.1:c.465del (PIGC))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.172411298del
DNA change (hg38) -
Published as PIGC(NM_153747.1):c.465delC (p.(Phe155fs))
ISCN -
DB-ID C1orf105_000005
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 2024-08-28 13:07:21 +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     
C1orf105 NM_139240.3 +?/. - c.22-2915del r.(=) p.(=)
PIGC NM_153747.1 +?/. - c.465del r.(?) p.(Phe155Leufs*4)


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