SULT1C2 sulfotransferase family 1C member 2
Information
- Symbol
- SULT1C2
- Type
- protein-coding
- Description
- sulfotransferase family 1C member 2
- Entrez Gene ID
- 6819
- Genome
- hg19
- Position
- chr2:108,905,095-108,926,371
- Genome
- hg38
- Position
- chr2:108,288,639-108,309,915
- MIM
- 602385 OMIM
- HGNC
- HGNC:11456 HGNC
- Ensembl
- ENSG00000198203 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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44 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | ST1C1 |
SYNONYM | ST1C2 |
SYNONYM | SULT1C1 |
SYNONYM | humSULTC2 |
MIM | 602385 OMIM |
HGNC | HGNC:11456 HGNC |
Ensembl | ENSG00000198203 Ensembl |
AllianceGenome | HGNC:11456 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409880.5 | hg38 | chr2 | 108,288,915 | 108,308,713 | 19,799 |
ENST00000251481.11 | hg38 | chr2 | 108,288,895 | 108,309,915 | 21,021 |
ENST00000326853.9 | hg38 | chr2 | 108,288,639 | 108,309,915 | 21,277 |
ENST00000437390.6 | hg38 | chr2 | 108,288,915 | 108,308,713 | 19,799 |
ENST00000326853.9 | hg19 | chr2 | 108,905,095 | 108,926,371 | 21,277 |
ENST00000251481.11 | hg19 | chr2 | 108,905,351 | 108,926,371 | 21,021 |
ENST00000409880.5 | hg19 | chr2 | 108,905,371 | 108,925,169 | 19,799 |
ENST00000437390.6 | hg19 | chr2 | 108,905,371 | 108,925,169 | 19,799 |
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