Variant #0000272556 (NC_000019.9:g.16606596C>T, NM_145046.4:c.159G>A (CALR3))

Chromosome 19
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.16606596C>T
DNA change (hg38) g.16495785C>T
Published as CALR3(NM_145046.4):c.159G>A (p.S53=), CALR3(NM_145046.5):c.159G>A (p.S53=)
ISCN -
DB-ID CALR3_000037 See all 2 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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHERP NM_006387.5 -?/. - c.*23374G>A r.(=) p.(=)
C19orf44 NM_032207.2 -?/. - c.-682C>T r.(?) p.(=)
CALR3 NM_145046.4 -?/. - c.159G>A r.(?) p.(Ser53=)


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