Variant #0000249911 (NC_000017.10:g.40716520A>G, NM_025233.6:c.972A>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.40716520A>G
DNA change (hg38) g.42564502A>G
Published as COASY(NM_025233.6):c.972A>G (p.T324=), COASY(NM_025233.7):c.972A>G (p.T324=)
ISCN -
DB-ID COASY_000006 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) 0.53198 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 2018-01-15 20:58:59 +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.*8466T>C r.(=) p.(=)
COASY NM_025233.6 -/. - c.972A>G r.(?) p.(Thr324=)
MLX NM_170607.2 -/. - c.-2623A>G r.(?) p.(=)


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