Variant #0000330157 (NC_000004.11:g.159590838del, NM_004453.2:c.-2771del (ETFDH))

Chromosome 4
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.159590838del
DNA change (hg38) g.158669686del
Published as C4orf46(NM_001008393.3):c.272del (p.?)
ISCN -
DB-ID C4orf46_000002
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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C4orf46 NM_001008393.2 ?/. - c.272del r.(?) p.(Asn91MetfsTer12)
ETFDH NM_004453.2 ?/. - c.-2771del r.(?) p.(=)


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