Variant #0000561519 (NC_000017.10:g.40715042G>T, NM_025233.6:c.402G>T (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.40715042G>T
DNA change (hg38) g.42563024G>T
Published as COASY(NM_025233.6):c.402G>T (p.V134=)
ISCN -
DB-ID COASY_000015
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) 1.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-13 13:58:52 +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.*9944C>A r.(=) p.(=)
COASY NM_025233.6 -?/. - c.402G>T r.(?) p.(Val134=)
MLX NM_170607.2 -?/. - c.-4101G>T r.(?) p.(=)


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