Variant #0000677045 (NC_000003.11:g.49455325C>T, NM_000481.3:c.959G>A (AMT))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49455325C>T
DNA change (hg38) -
Published as AMT(NM_000481.3):c.959G>A (p.(Arg320His), p.R320H)
ISCN -
DB-ID AMT_000024 See all 40 reported entries
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) 8.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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     
AMT NM_000481.3 +/. - c.959G>A r.(?) p.(Arg320His)
TCTA NM_022171.2 +/. - c.*3030C>T r.(=) p.(=)
NICN1 NM_032316.3 +/. - c.*6941G>A r.(=) p.(=)


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