Variant #0000272377 (NC_000009.11:g.139739247G>A, NM_024718.4:c.*4273G>A (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.139739247G>A
DNA change (hg38) g.136844795G>A
Published as AJM1(NM_001080482.3):c.381G>A (p.E127=)
ISCN -
DB-ID C9orf172_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-26 12:51:21 +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.381G>A r.(?) p.(Glu127=)
PHPT1 NM_014172.4 -?/. - c.-4636G>A r.(?) p.(=)
RABL6 NM_024718.4 -?/. - c.*4273G>A r.(=) p.(=)


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