Variant #0000326754 (NC_000019.9:g.51871284G>A, NM_001985.2:c.-1704C>T (ETFB))

Chromosome 19
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.51871284G>A
DNA change (hg38) g.51368030G>A
Published as CLDND2(NM_152353.2):c.170-4C>T (p.?)
ISCN -
DB-ID CLDND2_000001
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) 0.00046 View details
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 2020-07-16 11:19:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ETFB NM_001014763.1 ?/. - c.-13392C>T r.(?) p.(=)
ETFB NM_001985.2 ?/. - c.-1704C>T r.(?) p.(=)
NKG7 NM_005601.3 ?/. - c.*3747C>T r.(=) p.(=)
CLDND2 NM_152353.2 ?/. - c.170-4C>T r.spl? p.?


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