Variant #0000312006 (NC_000002.11:g.1481155G>T, NM_000547.5:c.1117G>T (TPO))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1481155G>T
DNA change (hg38) g.1477383G>T
Published as TPO(NM_000547.5):c.1117G>T (p.A373S), TPO(NM_000547.6):c.1117G>T (p.A373S)
ISCN -
DB-ID TPO_000010 See all 3 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) 0.4697 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPO NM_000547.5 -/. - c.1117G>T r.(?) p.(Ala373Ser)


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