Variant #0000273744 (NC_000017.10:g.40714804C>A, NM_025233.6:c.164C>A (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.40714804C>A
DNA change (hg38) g.42562786C>A
Published as COASY(NM_025233.6):c.164C>A (p.S55Y), COASY(NM_025233.7):c.164C>A (p.S55Y)
ISCN -
DB-ID COASY_000004 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) 0.53278 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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMC3IP NM_013290.6 -/. - c.*10182G>T r.(=) p.(=)
COASY NM_025233.6 -/. - c.164C>A r.(?) p.(Ser55Tyr)
MLX NM_170607.2 -/. - c.-4339C>A r.(?) p.(=)


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