Variant #0001024669 (NC_000002.11:g.70439942T>C, NM_022173.2:c.1070A>G (TIA1))

Chromosome 2
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.70439942T>C
DNA change (hg38) -
Published as TIA1(NM_022037.2):c.1037A>G (p.(Asn346Ser)), TIA1(NM_022173.4):c.1070A>G (p.N357S)
ISCN -
DB-ID TIA1_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) 0.00671 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 2025-02-07 18:57:27 +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     
TIA1 NM_022173.2 ?/. - c.1070A>G r.(?) p.(Asn357Ser)


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