Variant #0000613673 (NC_000011.9:g.695724G>C, NM_021008.2:c.-677C>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.695724G>C
DNA change (hg38) g.695724G>C
Published as DEAF1(NM_021008.4):c.-677C>G
ISCN -
DB-ID DEAF1_000063
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DEAF1 NM_021008.2 ?/. - c.-677C>G r.(?) p.(=)
EPS8L2 NM_022772.3 ?/. - c.-10643G>C r.(?) p.(=)
TMEM80 NM_174940.2 ?/. - c.-29G>C r.(?) p.(=)


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