Variant #0000552615 (NC_000014.8:g.51096713G>A, NM_015915.4:c.1552G>A (ATL1))

Chromosome 14
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.51096713G>A
DNA change (hg38) g.50629995G>A
Published as ATL1(NM_015915.5):c.1552G>A (p.G518R)
ISCN -
DB-ID SAV1_000001 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
ATL1 NM_015915.4 ?/. - c.1552G>A r.(?) p.(Gly518Arg)
SAV1 NM_021818.3 ?/. - c.*5188C>T r.(=) p.(=)


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