Variant #0000983713 (NC_000019.9:g.8455347C>T, NC_000019.9(NM_004218.3):c.40+7C>T (RAB11B))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.8455347C>T
DNA change (hg38) -
Published as RAB11B(NM_004218.4):c.40+7C>T
ISCN -
DB-ID RAB11B_000012
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) 0.0009 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB11B NM_004218.3 -/. - c.40+7C>T r.(=) p.(=)
RAB11B-AS1 NR_038237.1 -/. - n.229G>A r.(?) -


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