Variant #0000803437 (NC_000008.10:g.125555509G>A, NM_014751.4:c.*9724C>T (MTSS1))

Chromosome 8
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.125555509G>A
DNA change (hg38) -
Published as NDUFB9(NM_005005.2):c.283G>A (p.D95N)
ISCN -
DB-ID MTSS1_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) 8.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFB9 NM_005005.2 -?/. - c.283G>A r.(?) p.(Asp95Asn)
RNF139 NM_007218.3 -?/. - c.*55624G>A r.(=) p.(=)
MTSS1 NM_014751.4 -?/. - c.*9724C>T r.(=) p.(=)
TATDN1 NM_032026.3 -?/. - c.-4222C>T r.(?) p.(=)


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