GRCh38/hg38 16q12.1(chr16:47497444-48230506)x1 Detail (hg38) (PHKB, ABCC11, ABCC12, LINC02192, LINC02133, LINC02134, LOC112449713, LOC125146444, LOC126862336, LOC126862337, LOC126862338, LOC126862339, LOC130058949, LOC130058950, LOC130058951, LOC130058952)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr16:47,531,355-48,264,417 View the variant detail on this assembly version. |
hg38 | chr16:47,497,444-48,230,506 |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
ClinVar
Clinical Significance |
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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 |
---|---|---|---|---|---|
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2015-07-20 | no assertion criteria provided | Breast ductal adenocarcinoma |
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Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
GRCh38/hg38 16q12.1(chr16:47497444-48230506)x1 AND Breast ductal adenocarcinoma | ClinVar | Detail |
Overlapped Transcript Coordinates
Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
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Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- Genome
- hg38
- Position
- chr16:47,497,444-48,230,506
- Variant Type
- cnv
Genome browser