Variant #0000517768 (NC_000003.11:g.127786910G>A, NM_021937.3:c.-85441G>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.127786910G>A
DNA change (hg38) g.128068067G>A
Published as SEC61A1(NM_013336.3):c.1244+8G>A (p.(=))
ISCN -
DB-ID RUVBL1_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) 0.00077 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RUVBL1 NM_003707.2 -?/. - c.*13183C>T r.(=) p.(=)
SEC61A1 NM_013336.3 -?/. - c.1244+8G>A r.(=) p.(=)
EEFSEC NM_021937.3 -?/. - c.-85441G>A r.(?) p.(=)


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