Variant #0001037359 (NC_000009.11:g.139734940dup, NM_024718.4:c.2156dup (RABL6))

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.139734940dup
DNA change (hg38) -
Published as RABL6(NM_024718.5):c.2156dup (p.(His720Profs*160))
ISCN -
DB-ID C9orf172_000028
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C9orf172 NM_001080482.2 ?/. - c.-3927dup r.(?) p.(=)
RABL6 NM_024718.4 ?/. - c.2156dup r.(?) p.(His720Profs*160)


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