Variant #0000800955 (NC_000003.11:g.127785803C>A, NM_021937.3:c.-86548C>A (EEFSEC))

Chromosome 3
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.127785803C>A
DNA change (hg38) -
Published as SEC61A1(NM_013336.4):c.784C>A (p.R262=)
ISCN -
DB-ID RUVBL1_000008
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) 0.00067 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
RUVBL1 NM_003707.2 -?/. - c.*14290G>T r.(=) p.(=)
SEC61A1 NM_013336.3 -?/. - c.784C>A r.(?) p.(Arg262=)
EEFSEC NM_021937.3 -?/. - c.-86548C>A r.(?) p.(=)


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