Variant #0000676529 (NC_000002.11:g.220348261C>G, NM_005876.4:c.6076C>G (SPEG))

Chromosome 2
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.220348261C>G
DNA change (hg38) -
Published as SPEG(NM_005876.4):c.6076C>G (p.R2026G), SPEG(NM_005876.5):c.6076C>G (p.R2026G)
ISCN -
DB-ID SPEG_000011 See all 2 reported entries
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) 0.00172 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPEG NM_005876.4 -?/. - c.6076C>G r.(?) p.(Arg2026Gly)


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