Variant #0001041856 (NC_000017.10:g.40717732G>A, NM_025233.6:c.1541G>A (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.40717732G>A
DNA change (hg38) -
Published as COASY(NM_025233.7):c.1541G>A (p.(Arg514Gln))
ISCN -
DB-ID COASY_000037
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
PSMC3IP NM_013290.6 ?/. - c.*7254C>T r.(=) p.(=)
COASY NM_025233.6 ?/. - c.1541G>A r.(?) p.(Arg514Gln)
MLX NM_170607.2 ?/. - c.-1411G>A r.(?) p.(=)


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