Variant #0000532113 (NC_000007.13:g.47840310C>G, NM_138295.3:c.8130G>C (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.47840310C>G
DNA change (hg38) g.47800712C>G
Published as PKD1L1(NM_138295.5):c.8130G>C (p.(Gln2710His))
ISCN -
DB-ID C7orf69_000004
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) 0.02991 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 2019-07-18 18:22:55 +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.108+5269C>G r.(=) p.(=)
PKD1L1 NM_138295.3 -?/. - c.8130G>C r.(?) p.(Gln2710His)


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