Variant #0000983412 (NC_000019.9:g.38621330G>A, NM_015073.1:c.3061G>A (SIPA1L3))

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.38621330G>A
DNA change (hg38) -
Published as SIPA1L3(NM_015073.3):c.3061G>A (p.(Asp1021Asn))
ISCN -
DB-ID SIPA1L3_000059
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) 0.00013 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SIPA1L3 NM_015073.1 -?/. - c.3061G>A r.(?) p.(Asp1021Asn)


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