Variant #0000608813 (NC_000003.11:g.52842605G>T, NM_002217.3:c.2581G>T (ITIH3))

Chromosome 3
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.52842605G>T
DNA change (hg38) g.52808589G>T
Published as ITIH3(NM_002217.3):c.2581G>T (p.G861C)
ISCN -
DB-ID ITIH3_000002
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITIH3 NM_002217.3 ?/. - c.2581G>T r.(?) p.(Gly861Cys)
ITIH4 NM_002218.4 ?/. - c.*4832C>A r.(=) p.(=)


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