Variant #0000888057 (NC_000007.13:g.96635562_96635564del, NM_005222.3:c.273_275del (DLX6))

Chromosome 7
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.96635562_96635564del
DNA change (hg38) -
Published as DLX6(NM_005222.3):c.256_258del (p.(His91del))
ISCN -
DB-ID DLX6_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DLX6 NM_005222.3 -?/. - c.273_275del r.(?) p.(His91del)
DLX6-AS1 NR_015448.1 -?/. - n.141+7690_141+7692del r.(?) -


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