chr15:43023473:T>C Detail (hg19) (CDAN1)

Information

Genome

Assembly Position
hg19 chr15:43,023,473-43,023,473
hg38 chr15:42,731,275-42,731,275 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_138477.2:c.1796A>G NP_612486.2:p.Asn599Ser
Ensemble ENST00000356231.4:c.1796A>G ENST00000356231.4:p.Asn599Ser
Summary

MGeND

Clinical significance Pathogenic
Variant entry 3
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:<0.001
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 607465 OMIM
HGNC 1713 HGNC
Ensembl ENSG00000140326 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv52721423 TogoVar
COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
Pathogenic anemia, congenital dyserythropoietic germline MGS000001
(TMGS000138) 		Kenjiro Kosaki Keio University
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2003-07-01 no assertion criteria provided Congenital dyserythropoietic anemia, type I germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.362 Congenital dyserythropoietic anemia, type I NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_138477.4(CDAN1):c.1796A>G (p.Asn599Ser) AND Congenital dyserythropoietic anemia, type I ClinVar Detail
NA 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
rs120074166 dbSNP
Genome
hg19
Position
chr15:43,023,473-43,023,473
Variant Type
snv
Reference Allele
T
Alternative Allele
C
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))
rs120074166
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.0001
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
1
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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