Variant #0000322184 (NC_000011.9:g.31804960A>T, NM_000280.3:c.*6522T>A (PAX6))

Chromosome 11
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.31804960A>T
DNA change (hg38) g.31783412A>T
Published as ELP4(NM_019040.3):c.1163A>T (p.(Asp388Val))
ISCN -
DB-ID ELP4_000007
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAX6 NM_000280.3 -?/. - c.*6522T>A r.(=) p.(=)
ELP4 NM_019040.3 -?/. - c.1163A>T r.(?) p.(Asp388Val)


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