Variant #0000537492 (NC_000009.11:g.139734799_139734801del, NM_024718.4:c.2015_2017del (RABL6))

Chromosome 9
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.139734799_139734801del
DNA change (hg38) g.136840347_136840349del
Published as RABL6(NM_001173988.1):c.2018_2020delAGA (p.(Lys672del))
ISCN -
DB-ID C9orf172_000007
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C9orf172 NM_001080482.2 -?/. - c.-4068_-4066del r.(?) p.(=)
RABL6 NM_024718.4 -?/. - c.2015_2017del r.(?) p.(Lys672del)


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