Variant #0000525937 (NC_000005.9:g.68715242G>A, NM_001038603.2:c.30G>A (MARVELD2))

Chromosome 5
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.68715242G>A
DNA change (hg38) g.69419415G>A
Published as MARVELD2(NM_001038603.2):c.30G>A (p.R10=)
ISCN -
DB-ID MARVELD2_000013
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) 0.00021 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MARVELD2 NM_001038603.2 -?/. - c.30G>A r.(?) p.(Arg10=)
TAF9 NM_016283.4 -?/. - c.-49925C>T r.(?) p.(=)
RAD17 NM_133344.1 -?/. - c.*5123G>A r.(=) p.(=)


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