Variant #0000326165 (NC_000019.9:g.10445344del, NM_133452.2:c.-1109del (RAVER1))

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.10445344del
DNA change (hg38) g.10334668del
Published as ICAM3(NM_002162.3):c.1053delC (p.(Ala352fs))
ISCN -
DB-ID ICAM3_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ICAM3 NM_002162.3 ?/. - c.1053del r.(?) p.(Ala352ArgfsTer11)
RAVER1 NM_133452.2 ?/. - c.-1109del r.(?) p.(=)


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