Variant #0000345850 (NC_000003.11:g.127783720G>A, NM_021937.3:c.-88631G>A (EEFSEC))

Chromosome 3
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.127783720G>A
DNA change (hg38) g.128064877G>A
Published as -
ISCN -
DB-ID SEC61A1_000001
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.*16373C>T r.(=) p.(=)
SEC61A1 NM_013336.3 ?/. - c.617G>A r.(?) p.(Gly206Glu)
EEFSEC NM_021937.3 ?/. - c.-88631G>A r.(?) p.(=)


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