Variant #0000949736 (NC_000011.9:g.63396808C>T, NM_015459.3:c.1609G>A (ATL3))

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.63396808C>T
DNA change (hg38) -
Published as ATL3(NM_001290048.2):c.1555G>A (p.D519N), ATL3(NM_015459.5):c.1609G>A (p.D537N)
ISCN -
DB-ID ATL3_000023 See all 2 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) 0.00011 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATL3 NM_015459.3 -?/. - c.1609G>A r.(?) p.(Asp537Asn)


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