Variant #0001056010 (NC_000017.10:g.40714887G>T, NM_025233.6:c.247G>T (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.40714887G>T
DNA change (hg38) -
Published as COASY(NM_025233.7):c.247G>T (p.(Val83Phe))
ISCN -
DB-ID COASY_000038
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
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.*10099C>A r.(=) p.(=)
COASY NM_025233.6 ?/. - c.247G>T r.(?) p.(Val83Phe)
MLX NM_170607.2 ?/. - c.-4256G>T r.(?) p.(=)


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