GRCh38/hg38 15q21.2(chr15:52005056-52098273)x1 Detail (hg38) (MAPK6, LOC108281154, MAPK6-DT, LOC125078080, LOC125078081, LOC129390704, LOC130057068, LOC130057069, LOC130057070, LOC130057071, LOC130057072, LOC130057073, LOC130057074, LOC130057075, LOC130057076)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr15:52,297,253-52,390,470 View the variant detail on this assembly version. |
hg38 | chr15:52,005,056-52,098,273 |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
ClinVar
Clinical Significance |
![]() |
Review star | ![]() |
Show details |
Links
Type | Database | ID | Link |
---|---|---|---|
Gene | MIM | ||
HGNC | |||
Ensembl | |||
NCBI | |||
Gene Cards | |||
OncoKB |
Type | Database | ID | Link |
---|---|---|---|
Variant | TogoVar | ||
COSMIC | |||
MONDO |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
![]() |
2011-08-12 | criteria provided, single submitter |
![]() |
Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
GRCh38/hg38 15q21.2(chr15:52005056-52098273)x1 AND See cases | ClinVar | Detail |
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
- chr15:52,005,056-52,098,273
- Variant Type
- cnv
Genome browser