Variant #0000912880 (NC_000008.10:g.133883773G>A, NM_003235.4:c.455G>A (TG))

Chromosome 8
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.133883773G>A
DNA change (hg38) -
Published as TG(NM_003235.4):c.455G>A (p.R152H), TG(NM_003235.5):c.455G>A (p.R152H)
ISCN -
DB-ID TG_000010 See all 2 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) 0.00076 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLA NM_001045556.2 -?/. - c.*166996C>T r.(=) p.(=)
TG NM_003235.4 -?/. - c.455G>A r.(?) p.(Arg152His)


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