Variant #0001042745 (NC_000019.9:g.16606920C>G, NM_145046.4:c.21G>C (CALR3))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.16606920C>G
DNA change (hg38) -
Published as CALR3(NM_145046.5):c.21G>C (p.Q7H)
ISCN -
DB-ID CALR3_000059 See all 5 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) 3.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2025-05-05 21:14:00 +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     
CHERP NM_006387.5 ?/. - c.*23050G>C r.(=) p.(=)
C19orf44 NM_032207.2 ?/. - c.-358C>G r.(?) p.(=)
CALR3 NM_145046.4 ?/. - c.21G>C r.(?) p.(Gln7His)


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