Variant #0000321884 (NC_000011.9:g.695835C>T, NM_021008.2:c.-788G>A (DEAF1))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.695835C>T
DNA change (hg38) g.695835C>T
Published as TMEM80(NM_001042463.1):c.83C>T (p.(Ala76Val))
ISCN -
DB-ID TMEM80_000002
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) 0.00394 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DEAF1 NM_021008.2 ?/. - c.-788G>A r.(?) p.(=)
EPS8L2 NM_022772.3 ?/. - c.-10532C>T r.(?) p.(=)
TMEM80 NM_174940.2 ?/. - c.70+13C>T r.(=) p.(=)


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