Variant #0000923827 (NC_000003.11:g.127785979G>C, NM_021937.3:c.-86372G>C (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.127785979G>C
DNA change (hg38) -
Published as SEC61A1(NM_013336.4):c.960G>C (p.L320=)
ISCN -
DB-ID RUVBL1_000013
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) 1.0E-5 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 2023-04-16 21:50:28 +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.*14114C>G r.(=) p.(=)
SEC61A1 NM_013336.3 -?/. - c.960G>C r.(?) p.(Leu320=)
EEFSEC NM_021937.3 -?/. - c.-86372G>C r.(?) p.(=)


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