Variant #0001005244 (NC_000019.9:g.9074124_9074135dup, NM_024690.2:c.13312_13323dup (MUC16))

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.9074124_9074135dup
DNA change (hg38) -
Published as MUC16(NM_024690.2):c.13312_13323dupGATGTGTCCTGG (p.(Trp4441_Thr4442insAspValSerTrp))
ISCN -
DB-ID MUC16_000149
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 2024-08-28 13:16:32 +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     
MUC16 NM_024690.2 ?/. - c.13312_13323dup r.(?) p.(Asp4438_Trp4441dup)


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