Variant #0000982780 (NC_000017.10:g.7287546C>T, NM_020360.3:c.*6158G>A (PLSCR3))

Chromosome 17
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.7287546C>T
DNA change (hg38) -
Published as TNK1(NM_003985.6):c.840C>T (p.(Gly280=))
ISCN -
DB-ID PLSCR3_000003
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) 5.0E-5 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 2024-04-19 20:27:30 +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     
TNK1 NM_003985.4 ?/. - c.840C>T r.(?) p.(=)
PLSCR3 NM_020360.3 ?/. - c.*6158G>A r.(=) p.(=)


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