Variant #0000805105 (NC_000011.9:g.36594994del, NM_000448.2:c.140del (RAG1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.36594994del
DNA change (hg38) -
Published as RAG1(NM_000448.2):c.140delA (p.K47Rfs*35), RAG1(NM_000448.3):c.140delA (p.K47Rfs*35)
ISCN -
DB-ID RAG1_000064 See all 3 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-09-17 14:40:49 +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     
RAG1 NM_000448.2 +?/. - c.140del r.(?) p.(Lys47Argfs*35)


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