Variant #0000321866 (NC_000011.9:g.640138C>G, NM_021008.2:c.*4412G>C (DEAF1))

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.640138C>G
DNA change (hg38) g.640138C>G
Published as DRD4(NM_000797.3):c.889C>G (p.P297A, p.(Pro297Ala))
ISCN -
DB-ID DRD4_000031 See all 2 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) 0.00078 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
DRD4 NM_000797.3 -?/. - c.889C>G r.(?) p.(Pro297Ala) -
DEAF1 NM_021008.2 -?/. - c.*4412G>C r.(=) p.(=) -


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