Variant #0000566490 (NC_000019.9:g.16606630T>C, NM_145046.4:c.125A>G (CALR3))

Chromosome 19
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.16606630T>C
DNA change (hg38) g.16495819T>C
Published as CALR3(NM_145046.4):c.125A>G (p.N42S), CALR3(NM_145046.5):c.125A>G (p.N42S)
ISCN -
DB-ID C19orf44_000002 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) 0.00033 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 2019-07-18 18:22:55 +02:00 (CEST)
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.*23340A>G r.(=) p.(=)
C19orf44 NM_032207.2 -/. - c.-648T>C r.(?) p.(=)
CALR3 NM_145046.4 -/. - c.125A>G r.(?) p.(Asn42Ser)


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