Variant #0000798877 (NC_000001.10:g.161176364A>C, NM_004550.4:c.370A>C (NDUFS2))

Chromosome 1
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.161176364A>C
DNA change (hg38) -
Published as NDUFS2(NM_001166159.1):c.370A>C (p.I124L)
ISCN -
DB-ID ADAMTS4_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_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFS2 NM_004550.4 ?/. - c.370A>C r.(?) p.(Ile124Leu)
ADAMTS4 NM_005099.4 ?/. - c.-7947T>G r.(?) p.(=)


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