Variant #0000726370 (NC_000017.10:g.40716485T>A, NM_025233.6:c.937T>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.40716485T>A
DNA change (hg38) -
Published as COASY(NM_025233.7):c.937T>A (p.Y313N)
ISCN -
DB-ID COASY_000027
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 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.*8501A>T r.(=) p.(=)
COASY NM_025233.6 ?/. - c.937T>A r.(?) p.(Tyr313Asn)
MLX NM_170607.2 ?/. - c.-2658T>A r.(?) p.(=)


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