Variant #0000926918 (NC_000019.9:g.47983179_47983196dup, NM_007059.2:c.714_731dup (KPTN))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47983179_47983196dup
DNA change (hg38) -
Published as KPTN(NM_007059.2):c.714_731dupTCTGCAGATGTGGTCGGT (p.(Leu239_Val244dup)), KPTN(NM_007059.3):c.714_731dupTCTGCAGATGTGGTCGGT (p.M241_Q246dup), KPTN(N...)
ISCN -
DB-ID KPTN_000003 See all 3 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAPA NM_003827.3 +/. - c.*8352_*8369dup r.(=) p.(=)
KPTN NM_007059.2 +/. - c.714_731dup r.(?) p.(Met241_Gln246dup)


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