Variant #0000532139 (NC_000007.13:g.47892745A>G, NM_138295.3:c.4940T>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.47892745A>G
DNA change (hg38) g.47853147A>G
Published as PKD1L1(NM_138295.3):c.4940T>C (p.(Ile1647Thr)), PKD1L1(NM_138295.4):c.4940T>C (p.I1647T)
ISCN -
DB-ID C7orf69_000028 See all 2 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) 0.0024 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 2019-07-18 18:22:55 +02:00 (CEST)
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.*33550A>G r.(=) p.(=)
PKD1L1 NM_138295.3 ?/. - c.4940T>C r.(?) p.(Ile1647Thr)


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