Variant #0000561522 (NC_000017.10:g.40716080C>T, NM_025233.6:c.802C>T (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.40716080C>T
DNA change (hg38) g.42564062C>T
Published as COASY(NM_025233.6):c.802C>T (p.P268S)
ISCN -
DB-ID COASY_000018
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) 0.00027 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 2020-03-23 16:13:27 +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.*8906G>A r.(=) p.(=)
COASY NM_025233.6 ?/. - c.802C>T r.(?) p.(Pro268Ser)
MLX NM_170607.2 ?/. - c.-3063C>T r.(?) p.(=)


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