Variant #0001030154 (NC_000008.10:g.133882026G>A, NM_003235.4:c.229G>A (TG))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.133882026G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID TG_000006 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs142698837
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00075 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-04-01 12:31:02 +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     
TG NM_003235.4 +?/. - c.229G>A r.(?) p.(Gly77Ser)


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