Variant #0000260663 (NC_000006.11:g.32150702G>A, NM_030652.3:c.*14969G>A (EGFL8))

Chromosome 6
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.32150702G>A
DNA change (hg38) g.32182925G>A
Published as AGER(NM_001136.4):c.607C>T (p.R203C)
ISCN -
DB-ID AGER_000001
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 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 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGER NM_001136.4 -?/. - c.607C>T r.(?) p.(Arg203Cys)
PBX2 NM_002586.4 -?/. - c.*3457C>T r.(=) p.(=)
AGPAT1 NM_006411.3 -?/. - c.-7121C>T r.(?) p.(=)
RNF5 NM_006913.3 -?/. - c.*2599G>A r.(=) p.(=)
EGFL8 NM_030652.3 -?/. - c.*14969G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.