XRCC6 X-ray repair cross complementing 6
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
36 |
![]() |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | CTC75 |
SYNONYM | CTCBF |
SYNONYM | G22P1 |
SYNONYM | KU70 |
SYNONYM | ML8 |
SYNONYM | TLAA |
MIM | 152690 OMIM |
HGNC | HGNC:4055 HGNC |
Ensembl | ENSG00000196419 Ensembl |
AllianceGenome | HGNC:4055 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000360079.8 | hg38 | chr22 | 41,621,295 | 41,664,041 | 42,747 |
ENST00000402580.7 | hg38 | chr22 | 41,621,295 | 41,664,048 | 42,754 |
ENST00000359308.8 | hg38 | chr22 | 41,621,350 | 41,664,039 | 42,690 |
ENST00000428575.6 | hg38 | chr22 | 41,621,163 | 41,664,048 | 42,886 |
ENST00000405878.5 | hg38 | chr22 | 41,621,461 | 41,664,039 | 42,579 |
ENST00000405506.2 | hg38 | chr22 | 41,621,983 | 41,664,034 | 42,052 |
ENST00000428575.6 | hg19 | chr22 | 42,017,167 | 42,060,052 | 42,886 |
ENST00000360079.8 | hg19 | chr22 | 42,017,299 | 42,060,045 | 42,747 |
ENST00000402580.7 | hg19 | chr22 | 42,017,299 | 42,060,052 | 42,754 |
ENST00000359308.8 | hg19 | chr22 | 42,017,354 | 42,060,043 | 42,690 |
ENST00000405878.5 | hg19 | chr22 | 42,017,465 | 42,060,043 | 42,579 |
ENST00000405506.2 | hg19 | chr22 | 42,017,987 | 42,060,038 | 42,052 |
Genome browser