Variant #0000338482 (NC_000011.9:g.61197664G>A, NC_000011.9(NM_017841.2):c.36+10G>A (SDHAF2))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61197664G>A
DNA change (hg38) g.61430192G>A
Published as SDHAF2(NM_017841.2):c.36+10G>A
ISCN -
DB-ID SDHAF2_000013 See all 2 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) 0.00341 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     

Predict/SIFT     

Predicted     
SDHAF2 NM_017841.2 -/. - c.36+10G>A r.(=) p.(=) - -
CPSF7 NM_024811.3 -/. - c.-362C>T r.(?) p.(=) - -


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