Variant #0000525941 (NC_000005.9:g.68715423A>G, NM_001038603.2:c.211A>G (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.68715423A>G
DNA change (hg38) g.69419596A>G
Published as MARVELD2(NM_001038603.2):c.211A>G (p.I71V)
ISCN -
DB-ID MARVELD2_000017
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) 8.0E-5 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.211A>G r.(?) p.(Ile71Val)
TAF9 NM_016283.4 -?/. - c.-50106T>C r.(?) p.(=)
RAD17 NM_133344.1 -?/. - c.*5304A>G r.(=) p.(=)


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