GATA1 c.871-305C>T Detail (hg19) (GATA1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chrX:48,652,236-48,652,236 |
hg38 | chrX:48,793,829-48,793,829 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_002049.3:c.907C>T | NP_002040.1:p.Gln303Ter |
Ensemble | ENST00000376665.4:c.871-305C>T | |
ENST00000376670.9:c.907C>T | ENST00000376670.9:p.Gln303Ter |
Summary
MGeND
Clinical significance |
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Variant entry | 1 |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
MGeND
Clinical significance | Last evaluated | Condition | Origin | Submission ID | Submitter | Institute | Citation | Comment | Image |
---|---|---|---|---|---|---|---|---|---|
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Adenocarcinoma of stomach (disorder) |
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MGS000021
(TMGS000080) |
Manabu Muto | Kyoto University |
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
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
- -
- Genome
- hg19
- Position
- chrX:48,652,236-48,652,236
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
Genome browser