Variant #0000545331 (NC_000011.9:g.6661352C>T, NM_003737.2:c.1493G>A (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.6661352C>T
DNA change (hg38) g.6640121C>T
Published as DCHS1(NM_003737.2):c.1493G>A (p.R498Q, p.(Arg498Gln)), DCHS1(NM_003737.4):c.1493G>A (p.R498Q)
ISCN -
DB-ID DCHS1_000206 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) 0.00125 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DCHS1 NM_003737.2 -?/. - c.1493G>A r.(?) p.(Arg498Gln)


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