Variant #0000726372 (NC_000017.10:g.40717674C>G, NC_000017.10(NM_025233.6):c.1486-3C>G (COASY))

Chromosome 17
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.40717674C>G
DNA change (hg38) -
Published as COASY(NM_025233.7):c.1486-3C>G
ISCN -
DB-ID COASY_000008
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) 9.0E-5 View details
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.*7312G>C r.(=) p.(=)
COASY NM_025233.6 ?/. - c.1486-3C>G r.spl? p.?
MLX NM_170607.2 ?/. - c.-1469C>G r.(?) p.(=)


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