Variant #0000525938 (NC_000005.9:g.68715244del, NM_001038603.2:c.32del (MARVELD2))

Chromosome 5
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.68715244del
DNA change (hg38) g.69419417del
Published as -
ISCN -
DB-ID MARVELD2_000014
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_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 2022-11-01 13:01:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MARVELD2 NM_001038603.2 +/. - c.32del r.(?) p.(Asp11AlafsTer18)
TAF9 NM_016283.4 +/. - c.-49927del r.(?) p.(=)
RAD17 NM_133344.1 +/. - c.*5125del r.(?) p.(=)


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