Variant #0000924869 (NC_000008.10:g.38027334G>A, NM_004874.3:c.-7054G>A (BAG4))

Chromosome 8
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.38027334G>A
DNA change (hg38) -
Published as LSM1(NM_014462.3):c.217C>T (p.L73=)
ISCN -
DB-ID BAG4_000002
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) 4.0E-5 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 2023-04-16 21:50:28 +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     
BAG4 NM_004874.3 -?/. - c.-7054G>A r.(?) p.(=)
LSM1 NM_014462.2 -?/. - c.217C>T r.(?) p.(Leu73=)


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