Variant #0000951241 (NC_000019.9:g.16606833G>T, NC_000019.9(NM_145046.4):c.91+17C>A (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.16606833G>T
DNA change (hg38) -
Published as CALR3(NM_145046.5):c.91+17C>A
ISCN -
DB-ID C19orf44_000008
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-11-27 17:35:39 +01:00 (CET)
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.*23137C>A r.(=) p.(=)
C19orf44 NM_032207.2 -/. - c.-445G>T r.(?) p.(=)
CALR3 NM_145046.4 -/. - c.91+17C>A r.(=) p.(=)


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