Variant #0000857107 (NC_000001.10:g.161172234C>T, NM_004550.4:c.59C>T (NDUFS2))

Chromosome 1
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.161172234C>T
DNA change (hg38) -
Published as NDUFS2(NM_001166159.1):c.59C>T (p.P20L)
ISCN -
DB-ID ADAMTS4_000011
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) 5.0E-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 2022-05-09 15:51:19 +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     
NDUFS2 NM_004550.4 -?/. - c.59C>T r.(?) p.(Pro20Leu)
ADAMTS4 NM_005099.4 -?/. - c.-3817G>A r.(?) p.(=)


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