Variant #0000967720 (NC_000015.9:g.34163245_34163246del, NM_001036.3:c.*5818_*5819del (RYR3))

Chromosome 15
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.34163245_34163246del
DNA change (hg38) -
Published as AVEN(NM_020371.3):c.517-3_517-2delTA
ISCN -
DB-ID RYR3_000076
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RYR3 NM_001036.3 -/. - c.*5818_*5819del r.(=) p.(=)
CHRM5 NM_012125.3 -/. - c.-98514_-98513del r.(?) p.(=)
AVEN NM_020371.2 -/. - c.517-3_517-2del r.spl? p.?


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