Variant #0000689505 (NC_000005.9:g.2748986G>A, NM_001134222.1:c.836C>T (IRX2))

Chromosome 5
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.2748986G>A
DNA change (hg38) -
Published as IRX2(NM_033267.5):c.836C>T (p.P279L)
ISCN -
DB-ID C5orf38_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) 0.00019 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IRX2 NM_001134222.1 ?/. - c.836C>T r.(?) p.(Pro279Leu)
C5orf38 NM_178569.2 ?/. - c.-3393G>A r.(?) p.(=)


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