Variant #0000654725 (NC_000002.11:g.84670490C>T, NM_003849.3:c.236G>A (SUCLG1))

Chromosome 2
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.84670490C>T
DNA change (hg38) g.84443366C>T
Published as SUCLG1(NM_003849.3):c.236G>A (p.G79D), SUCLG1(NM_003849.4):c.236G>A (p.G79D)
ISCN -
DB-ID SUCLG1_000003 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) 0.00139 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
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     
SUCLG1 NM_003849.3 ?/. - c.236G>A r.(?) p.(Gly79Asp)


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