Variant #0001036408 (NC_000007.13:g.47921579C>G, NM_138295.3:c.3370G>C (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.47921579C>G
DNA change (hg38) -
Published as PKD1L1(NM_138295.5):c.3370G>C (p.(Glu1124Gln))
ISCN -
DB-ID C7orf69_000151
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.*62384C>G r.(=) p.(=)
PKD1L1 NM_138295.3 ?/. - c.3370G>C r.(?) p.(Glu1124Gln)


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