Variant #0000350296 (NC_000019.9:g.1912476G>A, NM_138422.2:c.430G>A (ADAT3))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1912476G>A
DNA change (hg38) g.1912477G>A
Published as ADAT3(NM_138422.4):c.430G>A (p.V144M)
ISCN -
DB-ID ADAT3_000001 See all 14 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCAMP4 NM_079834.2 +?/. - c.-41-2502G>A r.(=) p.(=)
ADAT3 NM_138422.2 +?/. - c.430G>A r.(?) p.(Val144Met)


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