Variant #0000332214 (NC_000008.10:g.98788171_98788186dup, NM_018407.4:c.207_222dup (LAPTM4B))

Chromosome 8
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.98788171_98788186dup
DNA change (hg38) g.97775943_97775958dup
Published as LAPTM4B(NM_018407.4):c.201_202insGGCGGGCTCCAGGCGA (p.(Ser75AlafsTer71))
ISCN -
DB-ID LAPTM4B_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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAPTM4B NM_018407.4 ?/. - c.207_222dup r.(?) p.(Ser75AlafsTer71)


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