Variant #0000851188 (NC_000006.11:g.32190472C>A, NM_004557.3:c.267G>T (NOTCH4))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32190472C>A
DNA change (hg38) -
Published as NOTCH4(NM_004557.3):c.267G>T (p.G89=)
ISCN -
DB-ID GPSM3_000015
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOTCH4 NM_004557.3 -?/. - c.267G>T r.(?) p.(Gly89=)
GPSM3 NM_022107.1 -?/. - c.-27545G>T r.(?) p.(=)


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