Variant #0000975755 (NC_000003.11:g.33118643_33118644insACCTCTTTT, NC_000003.11(NM_000404.2):c.76-4438_76-4437insAAAGAGGTA (GLB1))

Chromosome 3
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.33118643_33118644insACCTCTTTT
DNA change (hg38) -
Published as GLB1(NM_001317040.2):c.162_163insAAAGAGGTA (p.(Ala54_Pro55insLysGluVal))
ISCN -
DB-ID GLB1_000123
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLB1 NM_000404.2 ?/. - c.76-4438_76-4437insAAAGAGGTA r.(=) p.(=)
TMPPE NM_001039770.2 ?/. - c.*15683_*15684insAAAGAGGTA r.(=) p.(=)


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