Variant #0000982666 (NC_000017.10:g.59466001dup, NC_000017.10(NM_017679.3):c.2594-3337dup (BCAS3))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.59466001dup
DNA change (hg38) -
Published as BCAS3(NM_001320470.3):c.2682dup (p.(Gln895ThrfsTer9))
ISCN -
DB-ID BCAS3_000011
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     
BCAS3 NM_017679.3 -?/. - c.2594-3337dup r.(=) p.(=)


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