Variant #0000993259 (NC_000003.11:g.127786833A>G, NM_021937.3:c.-85518A>G (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.127786833A>G
DNA change (hg38) -
Published as SEC61A1(NM_013336.3):c.1175A>G (p.(Lys392Arg))
ISCN -
DB-ID RUVBL1_000015
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.*13260T>C r.(=) p.(=)
SEC61A1 NM_013336.3 ?/. - c.1175A>G r.(?) p.(Lys392Arg)
EEFSEC NM_021937.3 ?/. - c.-85518A>G r.(?) p.(=)


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