Variant #0000529940 (NC_000006.11:g.84566957T>G, NC_000006.11(NM_001009994.1):c.240-4T>G (RIPPLY2))

Chromosome 6
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.84566957T>G
DNA change (hg38) g.83857238T>G
Published as -
ISCN -
DB-ID CYB5R4_000001 See all 2 reported entries
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) 0.00064 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RIPPLY2 NM_001009994.1 +/. - c.240-4T>G r.spl? p.?
CYB5R4 NM_016230.3 +/. - c.-2545T>G r.(?) p.(=)


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