Variant #0000559247 (NC_000016.9:g.81129851G>A, NM_052892.3:c.*4877C>T (PKD1L2))

Chromosome 16
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.81129851G>A
DNA change (hg38) g.81096246G>A
Published as GCSH(NM_004483.4):c.33C>T (p.A11=)
ISCN -
DB-ID GCSH_000016
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_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 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCSH NM_004483.4 -?/. - c.33C>T r.(?) p.(Ala11=)
PKD1L2 NM_052892.3 -?/. - c.*4877C>T r.(=) p.(=)


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