Variant #0000330414 (NC_000005.9:g.68715456G>C, NM_001038603.2:c.244G>C (MARVELD2))

Chromosome 5
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.68715456G>C
DNA change (hg38) g.69419629G>C
Published as MARVELD2(NM_001038603.2):c.244G>C (p.(Val82Leu))
ISCN -
DB-ID MARVELD2_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 2018-01-15 20:58:59 +01:00 (CET)
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.244G>C r.(?) p.(Val82Leu)
TAF9 NM_016283.4 ?/. - c.-50139C>G r.(?) p.(=)
RAD17 NM_133344.1 ?/. - c.*5337G>C r.(=) p.(=)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.