Variant #0000997492 (NC_000009.11:g.130269185del, NM_138361.5:c.*4007del (LRSAM1))

Chromosome 9
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.130269185del
DNA change (hg38) -
Published as FAM129B(NM_022833.2):c.2180delG (p.(Ser727fs))
ISCN -
DB-ID FAM129B_000011
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
FAM129B NM_022833.2 ?/. - c.2180del r.(?) p.(Ser727Thrfs*26)
LRSAM1 NM_138361.5 ?/. - c.*4007del r.(?) p.(=)


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