Variant #0000517003 (NC_000002.11:g.84670528A>G, NC_000002.11(NM_003849.3):c.202-4T>C (SUCLG1))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.84670528A>G
DNA change (hg38) g.84443404A>G
Published as SUCLG1(NM_003849.3):c.202-4T>C, SUCLG1(NM_003849.4):c.202-4T>C
ISCN -
DB-ID SUCLG1_000004 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) 0.00162 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +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     
SUCLG1 NM_003849.3 -/. - c.202-4T>C r.spl? p.?


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