Variant #0000571850 (NC_000022.10:g.34046370C>T, NM_004737.4:c.391G>A (LARGE))

Chromosome 22
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.34046370C>T
DNA change (hg38) g.33650384C>T
Published as LARGE(NM_004737.4):c.391G>A (p.(Val131Ile)), LARGE1(NM_004737.6):c.391G>A (p.V131I), LARGE1(NM_004737.7):c.391G>A (p.V131I)
ISCN -
DB-ID LARGE_000069 See all 3 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) 0.00056 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LARGE NM_004737.4 -?/. - c.391G>A r.(?) p.(Val131Ile)


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