Variant #0000983198 (NC_000019.9:g.1241846_1241863dup, NM_000455.4:c.*14271_*14288dup (STK11))

Chromosome 19
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.1241846_1241863dup
DNA change (hg38) -
Published as ATP5F1D(NM_001687.5):c.-4_14dup (p.(Ala5_Leu6insAlaMetLeuProAlaAla))
ISCN -
DB-ID ATP5D_000005
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_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     
STK11 NM_000455.4 ?/. - c.*14271_*14288dup r.(=) p.(=)
ATP5D NM_001687.4 ?/. - c.-4_14dup r.? p.?
C19orf26 NM_152769.2 ?/. - c.-4121_-4104dup r.(?) p.(=)


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