Variant #0000273743 (NC_000017.10:g.40717672C>G, NC_000017.10(NM_025233.6):c.1486-5C>G (COASY))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.40717672C>G
DNA change (hg38) g.42565654C>G
Published as COASY(NM_025233.6):c.1486-5C>G, COASY(NM_025233.7):c.1486-5C>G
ISCN -
DB-ID COASY_000007 See all 2 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) 0.04801 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMC3IP NM_013290.6 -/. - c.*7314G>C r.(=) p.(=)
COASY NM_025233.6 -/. - c.1486-5C>G r.spl? p.?
MLX NM_170607.2 -/. - c.-1471C>G r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.