Variant #0000726371 (NC_000017.10:g.40717504_40717505dup, NM_025233.6:c.1403_1404dup (COASY))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.40717504_40717505dup
DNA change (hg38) -
Published as COASY(NM_025233.7):c.1403_1404dupTG (p.I469*)
ISCN -
DB-ID COASY_000023
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMC3IP NM_013290.6 +?/. - c.*7490_*7491dup r.(=) p.(=)
COASY NM_025233.6 +?/. - c.1403_1404dup r.(?) p.(Ile469Ter)
MLX NM_170607.2 +?/. - c.-1639_-1638dup r.(?) p.(=)


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