chr17:7669691:C>G Detail (hg38) (TP53)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr17:7,573,009-7,573,009 View the variant detail on this assembly version. |
hg38 | chr17:7,669,691-7,669,691 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000546.5:c.1101-1G>C | |
NM_001126112.2:c.1101-1G>C | ||
NM_001276760.1:c.1101-1G>C |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2021-07-01 | no assertion criteria provided | Gastric cancer |
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Detail |
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
- hg38
- Position
- chr17:7,669,691-7,669,691
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- G
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