Variant #0000690013 (NC_000007.13:g.47851578G>A, NM_138295.3:c.7418C>T (PKD1L1))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.47851578G>A
DNA change (hg38) -
Published as PKD1L1(NM_138295.4):c.7418C>T (p.S2473F)
ISCN -
DB-ID C7orf69_000089
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) 0.00103 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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     
C7orf69 NM_025031.2 ?/. - c.109-6046G>A r.(=) p.(=)
PKD1L1 NM_138295.3 ?/. - c.7418C>T r.(?) p.(Ser2473Phe)


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