Variant #0000787782 (NC_000001.10:g.100346211C>T, NM_000642.2:c.1759C>T (AGL))

Chromosome 1
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.100346211C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID AGL_000070 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs139488862
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00054 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-05-28 11:05:02 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGL NM_000642.2 ?/. - c.1759C>T r.(?) p.(His587Tyr)


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