Variant #0000566703 (NC_000019.9:g.1918134G>A, NM_138422.2:c.*4984G>A (ADAT3))

Chromosome 19
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.1918134G>A
DNA change (hg38) g.1918135G>A
Published as SCAMP4(NM_079834.2):c.145G>A (p.(Ala49Thr))
ISCN -
DB-ID ADAT3_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) 0.01128 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.145G>A r.(?) p.(Ala49Thr)
ADAT3 NM_138422.2 -?/. - c.*4984G>A r.(=) p.(=)


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