Variant #0000521083 (NC_000004.11:g.103826685T>A, NM_001008388.4:c.*18098T>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.103826685T>A
DNA change (hg38) g.102905528T>A
Published as SLC9B1(NM_001100874.2):c.1318A>T (p.(Lys440Ter))
ISCN -
DB-ID CISD2_000010
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 14:07:48 +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.*18098T>A r.(=) p.(=)
SLC9B1 NM_139173.3 -?/. - c.1318A>T r.(?) p.(Lys440Ter)
SLC9B2 NM_178833.4 -?/. - c.*120842A>T r.(=) p.(=)


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