chr5:33955673:T>C Detail (hg19) (SLC45A2)

Information

Genome

Assembly Position
hg19 chr5:33,955,673-33,955,673
hg38 chr5:33,955,568-33,955,568 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_016180.4:c.889-1064A>G
NM_001012509.3:c.889-1064A>G
NM_001297417.2:c.563-1064A>G
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.382
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 606202 OMIM
HGNC 16472 HGNC
Ensembl ENSG00000164175 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv20741343 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
0.005 SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder) Three single nucleotide polymorphisms (rs28777, rs35391, and rs16891982) in the ... BeFree 19710684 Detail
<0.001 SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder) Three single nucleotide polymorphisms (rs28777, rs35391, and rs16891982) in the ... BeFree 19710684 Detail
Annotation

Annotations

DescrptionSourceLinks
Three single nucleotide polymorphisms (rs28777, rs35391, and rs16891982) in the MATP gene (SLC45A2) ... DisGeNET Detail
Three single nucleotide polymorphisms (rs28777, rs35391, and rs16891982) in the MATP gene (SLC45A2) ... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs35391 dbSNP
Genome
hg19
Position
chr5:33,955,673-33,955,673
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))
rs35391
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.3819
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
6400
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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