Variant #0001014362 (NC_000007.13:g.47870813_47870814del, NC_000007.13(NM_138295.3):c.6473+2_6473+3del (PKD1L1))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47870813_47870814del
DNA change (hg38) -
Published as PKD1L1(NM_138295.5):c.6473+2_6473+3del, PKD1L1(NM_138295.5):c.6473+2_6473+3delTG
ISCN -
DB-ID C7orf69_000138 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C7orf69 NM_025031.2 +/. - c.*11618_*11619del r.(=) p.(=)
PKD1L1 NM_138295.3 +/. - c.6473+2_6473+3del r.spl? p.?


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