Variant #0000679178 (NC_000011.9:g.34153739A>G, NM_024662.2:c.1588A>G (NAT10))

Chromosome 11
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.34153739A>G
DNA change (hg38) -
Published as NAT10(NM_024662.2):c.1588A>G (p.M530V)
ISCN -
DB-ID ABTB2_000004
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) 0.0008 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAT10 NM_024662.2 -?/. - c.1588A>G r.(?) p.(Met530Val)
ABTB2 NM_145804.2 -?/. - c.*20195T>C r.(=) p.(=)


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