Variant #0000677134 (NC_000004.11:g.103790293C>T, NM_001008388.4:c.52C>T (CISD2))

Chromosome 4
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.103790293C>T
DNA change (hg38) -
Published as CISD2(NM_001008388.4):c.52C>T (p.(Leu18=)), CISD2(NM_001008388.5):c.52C>T (p.L18=)
ISCN -
DB-ID CISD2_000002 See all 3 reported entries
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) 0.00119 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CISD2 NM_001008388.4 -?/. - c.52C>T r.(?) p.(Leu18=)
UBE2D3 NM_181893.1 -?/. - c.-392G>A r.(?) p.(=)


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