Variant #0000284621 (NC_000016.9:g.81129822G>A, NM_052892.3:c.*4906C>T (PKD1L2))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.81129822G>A
DNA change (hg38) g.81096217G>A
Published as GCSH(NM_004483.4):c.62C>T (p.S21L)
ISCN -
DB-ID GCSH_000002 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) 0.54127 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
GCSH NM_004483.4 -/. - c.62C>T r.(?) p.(Ser21Leu)
PKD1L2 NM_052892.3 -/. - c.*4906C>T r.(=) p.(=)


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