Variant #0000803162 (NC_000007.13:g.47854969G>A, NM_138295.3:c.7052C>T (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.47854969G>A
DNA change (hg38) -
Published as PKD1L1(NM_138295.4):c.7052C>T (p.P2351L)
ISCN -
DB-ID C7orf69_000103
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) 0.00015 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 2021-09-17 14:40:49 +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.109-2655G>A r.(=) p.(=)
PKD1L1 NM_138295.3 -?/. - c.7052C>T r.(?) p.(Pro2351Leu)


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