Variant #0000975359 (NC_000002.11:g.54028956G>A, NM_016115.4:c.-15012C>T (ASB3))

Chromosome 2
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.54028956G>A
DNA change (hg38) -
Published as ERLEC1(NM_015701.5):c.856G>A (p.(Val286Met))
ISCN -
DB-ID ASB3_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) 0.00106 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     
CHAC2 NM_001008708.2 -?/. - c.*27294G>A r.(=) p.(=)
GPR75-ASB3 NM_001164165.1 -?/. - c.102-36234C>T r.(=) p.(=)
GPR75 NM_006794.3 -?/. - c.*51315C>T r.(=) p.(=)
ERLEC1 NM_015701.4 -?/. - c.856G>A r.(?) p.(Val286Met)
ASB3 NM_016115.4 -?/. - c.-15012C>T r.(?) p.(=)


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