Variant #0000691054 (NC_000011.9:g.34129773A>G, NM_024662.2:c.1A>G (NAT10))

Chromosome 11
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.34129773A>G
DNA change (hg38) -
Published as NAT10(NM_024662.2):c.1A>G (p.M1?)
ISCN -
DB-ID ABTB2_000006
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 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAT10 NM_024662.2 ?/. - c.1A>G r.(?) p.(Met1?)
ABTB2 NM_145804.2 ?/. - c.*44161T>C r.(=) p.(=)


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