Variant #0001042634 (NC_000019.9:g.13054627_13054628insTTGTC, NM_004343.3:c.1154_1155insTTGTC (CALR))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13054627_13054628insTTGTC
DNA change (hg38) -
Published as CALR(NM_004343.3):c.1154_1155insTTGTC (p.(Lys385AsnfsTer47))
ISCN -
DB-ID CALR_000003
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
CALR NM_004343.3 +/. - c.1154_1155insTTGTC r.(?) p.(Lys385Asnfs*47)
RAD23A NM_005053.3 +/. - c.-2136_-2135insTTGTC r.(?) p.(=)


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