Variant #0000543755 (NC_000011.9:g.31804978G>C, NM_000280.3:c.*6504C>G (PAX6))

Chromosome 11
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.31804978G>C
DNA change (hg38) g.31783430G>C
Published as ELP4(NM_001288725.1):c.1323G>C (p.E441D)
ISCN -
DB-ID ELP4_000014
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) 0.00574 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
PAX6 NM_000280.3 -/. - c.*6504C>G r.(=) p.(=)
ELP4 NM_019040.3 -/. - c.1181G>C r.(?) p.(Ser394Thr)


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