Variant #0000803169 (NC_000007.13:g.47968953C>T, NM_138295.3:c.908G>A (PKD1L1))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47968953C>T
DNA change (hg38) -
Published as PKD1L1(NM_138295.4):c.908G>A (p.R303Q), PKD1L1(NM_138295.5):c.908G>A (p.(Arg303Gln), p.R303Q)
ISCN -
DB-ID C7orf69_000093 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) 0.00387 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.*109758C>T r.(=) p.(=)
PKD1L1 NM_138295.3 -/. - c.908G>A r.(?) p.(Arg303Gln)


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