Variant #0000655054 (NC_000004.11:g.103790253G>A, NM_001008388.4:c.12G>A (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.103790253G>A
DNA change (hg38) g.102869096G>A
Published as CISD2(NM_001008388.5):c.12G>A (p.E4=)
ISCN -
DB-ID CISD2_000018
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) 0.00018 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 2020-03-23 16:13:27 +01:00 (CET)
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     
CISD2 NM_001008388.4 -?/. - c.12G>A r.(?) p.(Glu4=)
UBE2D3 NM_181893.1 -?/. - c.-352C>T r.(?) p.(=)


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