Variant #0000537486 (NC_000009.11:g.139701301G>T, NM_024718.4:c.-1348G>T (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.139701301G>T
DNA change (hg38) g.136806849G>T
Published as CCDC183(NM_001039374.4):c.1371G>T (p.(Met457Ile))
ISCN -
DB-ID KIAA1984_000003
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) 0.00204 View details
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 2020-06-26 12:49:36 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA1984 NM_001039374.4 -?/. - c.1371G>T r.(?) p.(Met457Ile)
RABL6 NM_024718.4 -?/. - c.-1348G>T r.(?) p.(=)
KIAA1984-AS1 NR_024580.1 -?/. - n.476C>A r.(?) -


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