Variant #0000999430 (NC_000011.9:g.694797G>C, NM_021008.2:c.251C>G (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.694797G>C
DNA change (hg38) -
Published as DEAF1(NM_021008.2):c.251C>G (p.(Pro84Arg)), DEAF1(NM_021008.3):c.251C>G (p.P84R)
ISCN -
DB-ID DEAF1_000047 See all 2 reported entries
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) 2.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DEAF1 NM_021008.2 ?/. - c.251C>G r.(?) p.(Pro84Arg)
EPS8L2 NM_022772.3 ?/. - c.-11570G>C r.(?) p.(=)


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