Variant #0000562130 (NC_000017.10:g.48172809G>A, NM_005501.2:c.*6180G>A (ITGA3))

Chromosome 17
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.48172809G>A
DNA change (hg38) g.50095445G>A
Published as PDK2(NM_002611.4):c.10G>A (p.V4M)
ISCN -
DB-ID ITGA3_000029
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 2019-07-18 18:22:55 +02:00 (CEST)
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     
PDK2 NM_002611.4 -?/. - c.10G>A r.(?) p.(Val4Met)
ITGA3 NM_005501.2 -?/. - c.*6180G>A r.(=) p.(=)
SAMD14 NM_174920.3 -?/. - c.*17448C>T r.(=) p.(=)


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