Variant #0000611107 (NC_000007.13:g.47886522C>T, NM_138295.3:c.5108G>A (PKD1L1))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47886522C>T
DNA change (hg38) g.47846924C>T
Published as PKD1L1(NM_138295.3):c.5108G>A (p.(Arg1703His)), PKD1L1(NM_138295.4):c.5108G>A (p.R1703H), PKD1L1(NM_138295.5):c.5108G>A (p.R1703H)
ISCN -
DB-ID C7orf69_000060 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) 0.00069 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +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.*27327C>T r.(=) p.(=)
PKD1L1 NM_138295.3 -?/. - c.5108G>A r.(?) p.(Arg1703His)


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