Variant #0000520597 (NC_000003.11:g.66432749G>A, NM_001164796.1:c.*4518G>A (SLC25A26))

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.66432749G>A
DNA change (hg38) g.66382325G>A
Published as LRIG1(NM_015541.2):c.2565C>T (p.T855=)
ISCN -
DB-ID SLC25A26_000010
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) 0.00013 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 2020-06-15 11:18:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A26 NM_001164796.1 -?/. - c.*4518G>A r.(=) p.(=)
LRIG1 NM_015541.2 -?/. - c.2565C>T r.(?) p.(Thr855=)


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