Variant #0000524654 (NC_000005.9:g.145246157_145246158del, NM_001080516.1:c.470_471del (GRXCR2))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.145246157_145246158del
DNA change (hg38) g.145866594_145866595del
Published as GRXCR2(NM_001080516.1):c.470_471delTG (p.L157Hfs*15)
ISCN -
DB-ID GRXCR2_000003
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 2020-06-17 18:09:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRXCR2 NM_001080516.1 +/. - c.470_471del r.(?) p.(Leu157HisfsTer15)


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