Variant #0000301541 (NC_000019.9:g.39075614G>A, NM_000540.2:c.14678G>A (RYR1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.39075614G>A
DNA change (hg38) g.38584974G>A
Published as RYR1(NM_000540.2):c.14678G>A (p.R4893Q)
ISCN -
DB-ID RYR1_000072 See all 4 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
RYR1 NM_000540.2 +?/. - c.14678G>A r.(?) p.(Arg4893Gln)
MAP4K1 NM_001042600.1 +?/. - c.*2774C>T r.(=) p.(=)


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