Variant #0000611338 (NC_000007.13:g.96635447_96635449dup, NM_005222.3:c.158_160dup (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.96635447_96635449dup
DNA change (hg38) g.97006135_97006137dup
Published as DLX6(NM_005222.3):c.135_137dup (p.(Pro53dup))
ISCN -
DB-ID DLX6_000004
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 2024-04-19 20:27:30 +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.158_160dup r.(?) p.(Pro53dup)
DLX6-AS1 NR_015448.1 -?/. - n.141+7814_141+7816dup r.(?) -


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