Variant #0000273745 (NC_000017.10:g.40715084C>G, NM_025233.6:c.444C>G (COASY))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.40715084C>G
DNA change (hg38) g.42563066C>G
Published as COASY(NM_025233.6):c.444C>G (p.A148=)
ISCN -
DB-ID COASY_000005
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) 0.00039 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 2020-07-13 13:59:05 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMC3IP NM_013290.6 -?/. - c.*9902G>C r.(=) p.(=)
COASY NM_025233.6 -?/. - c.444C>G r.(?) p.(Ala148=)
MLX NM_170607.2 -?/. - c.-4059C>G r.(?) p.(=)


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