Variant #0000525940 (NC_000005.9:g.68715388C>T, NM_001038603.2:c.176C>T (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.68715388C>T
DNA change (hg38) g.69419561C>T
Published as MARVELD2(NM_001038603.2):c.176C>T (p.P59L)
ISCN -
DB-ID MARVELD2_000016
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) 0.0005 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.176C>T r.(?) p.(Pro59Leu)
TAF9 NM_016283.4 ?/. - c.-50071G>A r.(?) p.(=)
RAD17 NM_133344.1 ?/. - c.*5269C>T r.(=) p.(=)


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