chr7:50561050:TCTC> Detail (hg38) (DDC)

Information

Genome

Assembly Position
hg19 chr7:50,628,747-50,628,750 
hg38 chr7:50,561,050-50,561,053

HGVS

Type Transcript Protein
RefSeq NM_000790.3:c.-65_-68delGAGA
NM_001242888.1:c.-65_-68delGAGA
NM_001082971.1:c.-29+4235_-29+4232delGAGA
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.503
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 107930 OMIM
HGNC 2719 HGNC
Ensembl ENSG00000132437 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv29252559 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.178 attention deficit hyperactivity disorder We have assessed variants in four genes, DDC (rs3837091 and rs3735273), DRD2 (rs... BeFree 24163823 Detail
Annotation

Annotations

DescrptionSourceLinks
We have assessed variants in four genes, DDC (rs3837091 and rs3735273), DRD2 (rs1800496, rs1801028, ... DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs3837091 dbSNP
Genome
hg38
Position
chr7:50,561,050-50,561,053
Variant Type
snv
Reference Allele
TCTC
Alternative Allele
-
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs3837091
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.5028
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
8426
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16758
Genome browser