Variant #0000687922 (NC_000001.10:g.161180187G>A, NM_004106.1:c.-4925G>A (FCER1G))

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.161180187G>A
DNA change (hg38) -
Published as NDUFS2(NM_001166159.1):c.866+8G>A
ISCN -
DB-ID NDUFS2_000005
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) 0.00189 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 2020-09-15 15:50:26 +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     
FCER1G NM_004106.1 -?/. - c.-4925G>A r.(?) p.(=)
NDUFS2 NM_004550.4 -?/. - c.866+8G>A r.(=) p.(=)
ADAMTS4 NM_005099.4 -?/. - c.-11770C>T r.(?) p.(=)


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