Variant #0000967307 (NC_000013.10:g.37573393C>T, NM_181503.2:c.-1550C>T (EXOSC8))

Chromosome 13
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.37573393C>T
DNA change (hg38) -
Published as ALG5(NM_013338.5):c.45G>A (p.L15=)
ISCN -
DB-ID ALG5_000011
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) 0.001 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG5 NM_013338.4 -?/. - c.45G>A r.(?) p.(=)
SUPT20H NM_017569.3 -?/. - c.*10453G>A r.(=) p.(=)
EXOSC8 NM_181503.2 -?/. - c.-1550C>T r.(?) p.(=)


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