Variant #0000611339 (NC_000007.13:g.96635526_96635531dup, NM_005222.3:c.237_242dup (DLX6))

Chromosome 7
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.96635526_96635531dup
DNA change (hg38) g.97006214_97006219dup
Published as DLX6(NM_005222.3):c.226_227insCGGCGG (p.(Ala82_Ala83dup))
ISCN -
DB-ID DLX6_000005
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 2019-12-04 15:24:38 +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     
DLX6 NM_005222.3 ?/. - c.237_242dup r.(?) p.(Ala82_Ala83dup)
DLX6-AS1 NR_015448.1 ?/. - n.141+7716_141+7721dup r.(?) -


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