Variant #0000721477 (NC_000007.13:g.47920346_47920347insC, NM_138295.3:c.3499_3500insG (PKD1L1))

Chromosome 7
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.47920346_47920347insC
DNA change (hg38) -
Published as PKD1L1(NM_138295.4):c.3499_3500insG (p.Y1167*)
ISCN -
DB-ID C7orf69_000100
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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     
C7orf69 NM_025031.2 +?/. - c.*61151_*61152insC r.(=) p.(=)
PKD1L1 NM_138295.3 +?/. - c.3499_3500insG r.(?) p.(Tyr1167*)


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