SERF2 small EDRK-rich factor 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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14 |
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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
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MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | 4F5REL |
SYNONYM | FAM2C |
SYNONYM | H4F5REL |
SYNONYM | HsT17089 |
MIM | 605054 OMIM |
HGNC | HGNC:10757 HGNC |
Ensembl | ENSG00000140264 Ensembl |
AllianceGenome | HGNC:10757 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409291.5 | hg38 | chr15 | 43,792,347 | 43,800,279 | 7,933 |
ENST00000403425.5 | hg38 | chr15 | 43,792,368 | 43,794,046 | 1,679 |
ENST00000409614.1 | hg38 | chr15 | 43,792,839 | 43,794,046 | 1,208 |
ENST00000249786.9 | hg38 | chr15 | 43,792,320 | 43,796,079 | 3,760 |
ENST00000402131.5 | hg38 | chr15 | 43,792,368 | 43,793,975 | 1,608 |
ENST00000409960.6 | hg38 | chr15 | 43,792,330 | 43,794,444 | 2,115 |
ENST00000630046.2 | hg38 | chr15 | 43,791,842 | 43,799,079 | 7,238 |
ENST00000339624.9 | hg38 | chr15 | 43,792,347 | 43,794,046 | 1,700 |
ENST00000409646.5 | hg38 | chr15 | 43,792,330 | 43,799,850 | 7,521 |
ENST00000381359.5 | hg38 | chr15 | 43,777,100 | 43,794,595 | 17,496 |
ENST00000381359.5 | hg19 | chr15 | 44,069,298 | 44,086,793 | 17,496 |
ENST00000249786.9 | hg19 | chr15 | 44,084,518 | 44,088,277 | 3,760 |
ENST00000339624.9 | hg19 | chr15 | 44,084,545 | 44,086,244 | 1,700 |
ENST00000630046.2 | hg19 | chr15 | 44,084,040 | 44,091,277 | 7,238 |
ENST00000409960.6 | hg19 | chr15 | 44,084,528 | 44,086,642 | 2,115 |
ENST00000409646.5 | hg19 | chr15 | 44,084,528 | 44,092,048 | 7,521 |
ENST00000409291.5 | hg19 | chr15 | 44,084,545 | 44,092,477 | 7,933 |
ENST00000402131.5 | hg19 | chr15 | 44,084,566 | 44,086,173 | 1,608 |
ENST00000403425.5 | hg19 | chr15 | 44,084,566 | 44,086,244 | 1,679 |
ENST00000409614.1 | hg19 | chr15 | 44,085,037 | 44,086,244 | 1,208 |
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