Variant #0000611098 (NC_000007.13:g.47847951G>T, NM_138295.3:c.7721C>A (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.47847951G>T
DNA change (hg38) g.47808353G>T
Published as PKD1L1(NM_138295.5):c.7721C>A (p.A2574E)
ISCN -
DB-ID C7orf69_000052
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.109-9673G>T r.(=) p.(=)
PKD1L1 NM_138295.3 ?/. - c.7721C>A r.(?) p.(Ala2574Glu)


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