Variant #0000950939 (NC_000017.10:g.48155470G>A, NM_005501.2:c.2200G>A (ITGA3))

Chromosome 17
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.48155470G>A
DNA change (hg38) -
Published as ITGA3(NM_002204.4):c.2200G>A (p.V734M), ITGA3(NM_005501.2):c.2200G>A (p.(Val734Met))
ISCN -
DB-ID ITGA3_000041 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) 0.00089 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 2023-11-27 17:35:39 +01:00 (CET)
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     
ITGA3 NM_005501.2 ?/. - c.2200G>A r.(?) p.(Val734Met)


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