Variant #0000994274 (NC_000004.11:g.36345224_36345232del, NM_001170700.2:c.2124_2132del (DTHD1))

Chromosome 4
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.36345224_36345232del
DNA change (hg38) -
Published as DTHD1(NM_001170700.2):c.2124_2132delTCAGCTCAT (p.(Gln709_Ile711del)), DTHD1(NM_001170700.3):c.2499_2507delTCAGCTCAT (p.Q834_I836del)
ISCN -
DB-ID DTHD1_000006 See all 3 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) 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 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     
DTHD1 NM_001170700.2 -?/. - c.2124_2132del r.(?) p.(Gln709_Ile711del)


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