Variant #0000251378 (NC_000006.11:g.32130320A>G, NM_030652.3:c.-2143A>G (EGFL8))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32130320A>G
DNA change (hg38) g.32162543A>G
Published as PPT2(NM_138717.3):c.729-25A>G
ISCN -
DB-ID PPT2_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) 0.01003 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGPAT1 NM_006411.3 -/. - c.*6733T>C r.(=) p.(=)
EGFL8 NM_030652.3 -/. - c.-2143A>G r.(?) p.(=)
PPT2 NM_138717.2 -/. - c.729-25A>G r.(=) p.(=)
PPT2-EGFL8 NR_037861.1 -/. - n.1125-25A>G r.(?) -


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