Variant #0000553995 (NC_000015.9:g.34160031T>G, NM_001036.3:c.*2604T>G (RYR3))

Chromosome 15
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.34160031T>G
DNA change (hg38) g.33867830T>G
Published as AVEN(NM_020371.2):c.638A>C (p.(Gln213Pro))
ISCN -
DB-ID RYR3_000036
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) 0.00073 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RYR3 NM_001036.3 -?/. - c.*2604T>G r.(=) p.(=)
CHRM5 NM_012125.3 -?/. - c.-101728T>G r.(?) p.(=)
AVEN NM_020371.2 -?/. - c.638A>C r.(?) p.(Gln213Pro)


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