Variant #0001004284 (NC_000019.9:g.10445278A>C, NM_133452.2:c.-1044T>G (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.10445278A>C
DNA change (hg38) -
Published as ICAM3(NM_002162.3):c.1118T>G (p.(Phe373Cys))
ISCN -
DB-ID ICAM3_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) 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ICAM3 NM_002162.3 ?/. - c.1118T>G r.(?) p.(Phe373Cys)
RAVER1 NM_133452.2 ?/. - c.-1044T>G r.(?) p.(=)


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