chr17:42360972:C>G Detail (hg38) (STAT3)

Information

Genome

Assembly Position
hg19 chr17:40,512,990-40,512,990 View the variant detail on this assembly version.
hg38 chr17:42,360,972-42,360,972

HGVS

Type Transcript Protein
RefSeq NM_003150.3:c.-23-12433G>C
NM_139276.2:c.-23-12433G>C
NM_213662.1:c.-4-12452G>C
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.026
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 102582 OMIM
HGNC 11364 HGNC
Ensembl ENSG00000168610 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv57810193 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
<0.001 thyroiditis We genotyped six single-nucleotide polymorphisms (SNPs) rs1053005, rs2293152, rs... BeFree 24081513 Detail
<0.001 Graves Disease We genotyped six single-nucleotide polymorphisms (SNPs) rs1053005, rs2293152, rs... BeFree 24081513 Detail
Annotation

Annotations

DescrptionSourceLinks
We genotyped six single-nucleotide polymorphisms (SNPs) rs1053005, rs2293152, rs744166, rs17593222, ... DisGeNET Detail
We genotyped six single-nucleotide polymorphisms (SNPs) rs1053005, rs2293152, rs744166, rs17593222, ... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs17593222 dbSNP
Genome
hg38
Position
chr17:42,360,972-42,360,972
Variant Type
snv
Reference Allele
C
Alternative Allele
G
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))
rs17593222
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.0261
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
438
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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