Variant #0000678112 (NC_000007.13:g.47879085G>A, NM_138295.3:c.5728C>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.47879085G>A
DNA change (hg38) -
Published as PKD1L1(NM_138295.4):c.5728C>T (p.R1910W), PKD1L1(NM_138295.5):c.5728C>T (p.R1910W)
ISCN -
DB-ID C7orf69_000020 See all 3 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) 5.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
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.*19890G>A r.(=) p.(=)
PKD1L1 NM_138295.3 ?/. - c.5728C>T r.(?) p.(Arg1910Trp)


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