Variant #0000532154 (NC_000007.13:g.47933652T>A, NM_138295.3:c.2276A>T (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.47933652T>A
DNA change (hg38) g.47894055T>A
Published as PKD1L1(NM_138295.3):c.2276A>T (p.(Gln759Leu))
ISCN -
DB-ID C7orf69_000042
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) 0.00058 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C7orf69 NM_025031.2 ?/. - c.*74457T>A r.(=) p.(=)
PKD1L1 NM_138295.3 ?/. - c.2276A>T r.(?) p.(Gln759Leu)


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