Variant #0000914101 (NC_000013.10:g.37573407G>C, NM_181503.2:c.-1536G>C (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.37573407G>C
DNA change (hg38) -
Published as ALG5(NM_013338.5):c.31C>G (p.L11V)
ISCN -
DB-ID ALG5_000009
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) 0.00102 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 2023-01-11 15:44:22 +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.31C>G r.(?) p.(Leu11Val)
SUPT20H NM_017569.3 -?/. - c.*10439C>G r.(=) p.(=)
EXOSC8 NM_181503.2 -?/. - c.-1536G>C r.(?) p.(=)


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