Variant #0000563862 (NC_000017.10:g.902099C>T, NM_021962.3:c.*7221G>A (ABR))

Chromosome 17
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.902099C>T
DNA change (hg38) g.998859C>T
Published as TIMM22(NM_013337.2):c.319C>T (p.(Arg107Cys))
ISCN -
DB-ID TIMM22_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) 0.00032 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TIMM22 NM_013337.2 ?/. - c.319C>T r.(?) p.(Arg107Cys)
ABR NM_021962.3 ?/. - c.*7221G>A r.(=) p.(=)


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