Variant #0000851799 (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 TG(NM_003235.4):c.229G>A (p.G77S, p.(Gly77Ser)), TG(NM_003235.5):c.229G>A (p.G77S)
ISCN -
DB-ID TG_000006 See all 4 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) 0.00075 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLA NM_001045556.2 +?/. - c.*168743C>T r.(=) p.(=)
TG NM_003235.4 +?/. - c.229G>A r.(?) p.(Gly77Ser)


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