Variant #0000613625 (NC_000011.9:g.6662769_6662771dup, NM_003737.2:c.97_99dup (DCHS1))

Chromosome 11
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.6662769_6662771dup
DNA change (hg38) g.6641538_6641540dup
Published as DCHS1(NM_003737.2):c.95_97dupCTG (p.L33dup), DCHS1(NM_003737.2):c.97_99dup (p.(Leu33dup)), DCHS1(NM_003737.2):c.97_99dupCTG (p.L33dup), DCHS1(NM_0...)
ISCN -
DB-ID DCHS1_000224 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DCHS1 NM_003737.2 -?/. - c.97_99dup r.(?) p.(Leu33dup)


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