Variant #0000996546 (NC_000007.13:g.47852885T>C, NM_138295.3:c.7180A>G (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.47852885T>C
DNA change (hg38) -
Published as PKD1L1(NM_138295.3):c.7180A>G (p.(Arg2394Gly))
ISCN -
DB-ID C7orf69_000132
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) 0.00201 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.109-4739T>C r.(=) p.(=)
PKD1L1 NM_138295.3 -?/. - c.7180A>G r.(?) p.(Arg2394Gly)


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