Variant #0000513995 (NC_000002.11:g.207014677_207014682del, NC_000002.11(NM_005006.6):c.154-14_154-9del (NDUFS1))

Chromosome 2
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.207014677_207014682del
DNA change (hg38) g.206149953_206149958del
Published as NDUFS1(NM_005006.7):c.154-14_154-9delTTTTTT
ISCN -
DB-ID NDUFS1_000028
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFS1 NM_005006.6 -/. - c.154-14_154-9del r.(=) p.(=)


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