Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 143279 |
|---|---|
| ensemblid | ENSG00000165338.17 |
| hgncid | 26736 |
| symbol | HECTD2 |
| name | HECT domain E3 ubiquitin protein ligase 2 |
| refseq_nuc | NM_182765.6 |
| refseq_prot | NP_877497.4 |
| ensembl_nuc | ENST00000298068.10 |
| ensembl_prot | ENSP00000298068.5 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 91410344 |
| end | 91514820 |
| strand | + |
| ver | v1.2 |
| region | chr10:91410344-91514820 |
| region5000 | chr10:91405344-91519820 |
| regionname0 | HECTD2_chr10_91410344_91514820 |
| regionname5000 | HECTD2_chr10_91405344_91519820 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 776 | 14 | 10 | 4 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| a0002 | 1/0 | 776 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2331 | 9 | 8 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| c0002 | 0/0 | 2331 | 4 | 2 | 2 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| c0003 | 1/0 | 2331 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| c0004 | 0/0 | 2331 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2532 | 5 | 4 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| t0002 | 1/0 | 2532 | 5 | 2 | 2 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| t0003 | 0/0 | 2532 | 4 | 3 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| t0004 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2331 | 9 | 8 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| a0001c0002 | 0/0 | 2331 | 4 | 2 | 2 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| a0001c0004 | 0/0 | 2331 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| a0002c0003 | 1/0 | 2331 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4862 | 4 | 4 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| a0001c0001t0003 | 0/0 | 4862 | 4 | 3 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| a0001c0001t0004 | 0/0 | 4862 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| a0001c0002t0002 | 0/0 | 4862 | 4 | 2 | 2 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| a0001c0004t0001 | 0/0 | 4862 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| a0002c0003t0002 | 1/0 | 4862 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | copy fasta | chr10 | 91405344 | 91519820 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| a0001c0002t0002g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| a0001c0002t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| a0001c0002t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| a0001c0004t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| a0002c0003t0002g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| HG01081 | hp2 | a0001 | c0004 | t0001 | g0011 | AMR | PUR | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | LWK | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | USA | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | USA | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| homoSapiens_grch38 | hp1 | a0002 | c0003 | t0002 | g0014 | REF | REF | HECTD2_chr10_91405344_91519820 | HECTD2 | chr10 | 91405344 | 91519820 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:91410493
|
C | G | 1 | a0001 | 14 | HG01081.hp1 HG01081.hp2 HG01433.hp1 others(11): Show |
missense_variant | MODERATE | c.55C>G | p.Pro19Ala | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/21 | 150/4862 | 55/2331 | 19/776 | chr10 | 91410493 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:91425367
|
C | T | 1 | a0001c0004 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.225C>T | p.Asn75Asn | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/21 | 320/4862 | 225/2331 | 75/776 | chr10 | 91425367 | ||
| chr10:91461320
|
G | A | 2 | a0001c0001a0001c0004 | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
synonymous_variant | LOW | c.474G>A | p.Thr158Thr | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 4/21 | 569/4862 | 474/2331 | 158/776 | chr10 | 91461320 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:91512695
|
T | G | 3 | a0001c0001t0001a0001c0001t0003a0001c0004t0001 | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*311T>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 21/21 | 311 | chr10 | 91512695 | |||||
| chr10:91512742
|
G | A | 1 | a0001c0001t0003 | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*358G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 21/21 | 358 | chr10 | 91512742 | |||||
| chr10:91514035
|
T | G | 4 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1651T>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 21/21 | 1651 | chr10 | 91514035 | |||||
| chr10:91514614
|
A | G | 4 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2230A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 21/21 | 2230 | chr10 | 91514614 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:91410608
|
CG | C | 13 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(10): Show | 14 | HG01081.hp1 HG01081.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+34delG | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91410608 | |||||
| chr10:91411010
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+434C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91411010 | ||||||
| chr10:91412007
|
A | AGTG | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+1431_138+1432i others(5): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91412007 | ||||||
| chr10:91412455
|
G | GT | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+1891dupT | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91412455 | |||||
| chr10:91412631
|
A | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0003g0007others(5): Show | 8 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+2055A>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91412631 | ||||||
| chr10:91412668
|
A | ATGTG | 2 | a0001c0002t0002g0001a0001c0002t0002g0002 | 3 | HG01081.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.138+2116_138+2119d others(6): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91412668 | |||||
| chr10:91412668
|
A | ATGTGTG | 5 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(2): Show | 5 | HG01433.hp1 HG01433.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+2114_138+2119d others(8): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91412668 | |||||
| chr10:91412668
|
A | ATGTGTGT others(3): Show |
1 | a0001c0004t0001g0011 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.138+2110_138+2119d others(12): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91412668 | |||||
| chr10:91412668
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0001g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.138+2108_138+2119d others(14): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91412668 | |||||
| chr10:91412668
|
A | ATGTGTGT others(7): Show |
2 | a0001c0001t0001g0004a0001c0001t0004g0013 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.138+2106_138+2119d others(16): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91412668 | |||||
| chr10:91412668
|
A | ATGTGTGT others(9): Show |
1 | a0001c0001t0001g0005 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.138+2104_138+2119d others(18): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91412668 | |||||
| chr10:91412855
|
G | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG01081.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+2279G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91412855 | ||||||
| chr10:91414323
|
A | G | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+3747A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91414323 | ||||||
| chr10:91414920
|
C | G | 13 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(10): Show | 14 | HG01081.hp1 HG01081.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+4344C>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91414920 | ||||||
| chr10:91415193
|
A | AGTGT | 5 | a0001c0001t0001g0012a0001c0001t0003g0007a0001c0001t0003g0008others(2): Show | 5 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+4652_138+4655d others(6): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91415193 | |||||
| chr10:91415193
|
A | AGTGTGTG others(3): Show |
1 | a0001c0001t0001g0005 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.138+4646_138+4655d others(12): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91415193 | |||||
| chr10:91415193
|
A | AGTGTGTG others(5): Show |
2 | a0001c0001t0001g0006a0001c0001t0004g0013 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.138+4644_138+4655d others(14): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91415193 | |||||
| chr10:91415193
|
A | AGTGTGTG others(9): Show |
1 | a0001c0004t0001g0011 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.138+4640_138+4655d others(18): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91415193 | |||||
| chr10:91415632
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+5056C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91415632 | ||||||
| chr10:91415977
|
TGTAAAGT others(34): Show |
T | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.138+5430_138+5470d others(43): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91415977 | |||||
| chr10:91415996
|
CTTTTTTT others(35): Show |
C | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+5443_138+5484d others(44): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91415996 | |||||
| chr10:91416037
|
CT | C | 4 | a0001c0001t0004g0013a0001c0002t0002g0001a0001c0002t0002g0002others(1): Show | 5 | HG01081.hp1 HG01433.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+5471delT | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91416037 | |||||
| chr10:91416196
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+5620C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91416196 | ||||||
| chr10:91416581
|
ACT | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+6008_138+6009d others(4): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91416581 | |||||
| chr10:91416661
|
A | G | 2 | a0001c0002t0002g0001a0001c0002t0002g0003 | 3 | HG01081.hp1 HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.138+6085A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91416661 | ||||||
| chr10:91417470
|
T | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+6894T>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91417470 | ||||||
| chr10:91418112
|
GAA | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-7165_139-7164d others(4): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91418112 | |||||
| chr10:91418678
|
C | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-6603C>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91418678 | ||||||
| chr10:91418680
|
A | G | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.139-6601A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91418680 | ||||||
| chr10:91418712
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.139-6569G>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91418712 | ||||||
| chr10:91419322
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-5959A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91419322 | ||||||
| chr10:91419420
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-5861G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91419420 | ||||||
| chr10:91420280
|
CA | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01433.hp2 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-4986delA | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91420280 | |||||
| chr10:91420288
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.139-4993A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91420288 | ||||||
| chr10:91420429
|
C | CA | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-4839dupA | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91420429 | |||||
| chr10:91420448
|
G | C | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.139-4833G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91420448 | ||||||
| chr10:91420466
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-4815A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91420466 | ||||||
| chr10:91420496
|
G | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-4785G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91420496 | ||||||
| chr10:91420592
|
G | GA | 2 | a0001c0002t0002g0001a0001c0002t0002g0003 | 3 | HG01081.hp1 HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.139-4676dupA | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91420592 | |||||
| chr10:91421403
|
T | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-3878T>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91421403 | ||||||
| chr10:91421602
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.139-3679G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91421602 | ||||||
| chr10:91422074
|
T | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-3207T>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91422074 | ||||||
| chr10:91423701
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-1580C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | chr10 | 91423701 | ||||||
| chr10:91424452
|
TA | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-825delA | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr10 | 91424452 | |||||
| chr10:91425533
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.268+123C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91425533 | ||||||
| chr10:91426505
|
T | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+1095T>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91426505 | ||||||
| chr10:91426567
|
T | TAC | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(3): Show | 6 | HG01081.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+1173_268+1174d others(4): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 91426567 | |||||
| chr10:91426567
|
T | TACAC | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+1171_268+1174d others(6): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 91426567 | |||||
| chr10:91426637
|
T | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+1227T>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91426637 | ||||||
| chr10:91426974
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+1564G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91426974 | ||||||
| chr10:91427006
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+1596C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91427006 | ||||||
| chr10:91427717
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(1): Show | 4 | HG01081.hp2 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+2307T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91427717 | ||||||
| chr10:91428335
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268+2925G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91428335 | ||||||
| chr10:91428403
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+2993G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91428403 | ||||||
| chr10:91428835
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+3425C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91428835 | ||||||
| chr10:91428921
|
C | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268+3511C>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91428921 | ||||||
| chr10:91429132
|
A | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+3722A>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91429132 | ||||||
| chr10:91429428
|
C | G | 2 | a0001c0002t0002g0001a0001c0002t0002g0003 | 3 | HG01081.hp1 HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.268+4018C>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91429428 | ||||||
| chr10:91429585
|
A | C | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268+4175A>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91429585 | ||||||
| chr10:91429756
|
G | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+4346G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91429756 | ||||||
| chr10:91430193
|
G | A | 2 | a0001c0002t0002g0001a0001c0002t0002g0003 | 3 | HG01081.hp1 HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.268+4783G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91430193 | ||||||
| chr10:91430428
|
T | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+5018T>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91430428 | ||||||
| chr10:91430769
|
C | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+5359C>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91430769 | ||||||
| chr10:91430834
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+5424G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91430834 | ||||||
| chr10:91430850
|
G | C | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+5440G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91430850 | ||||||
| chr10:91431018
|
A | C | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+5608A>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91431018 | ||||||
| chr10:91431104
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.268+5694G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91431104 | ||||||
| chr10:91431208
|
A | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+5798A>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91431208 | ||||||
| chr10:91431613
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+6203A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91431613 | ||||||
| chr10:91431670
|
A | G | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268+6260A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91431670 | ||||||
| chr10:91431688
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+6278T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91431688 | ||||||
| chr10:91432299
|
G | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+6889G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91432299 | ||||||
| chr10:91432419
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+7009A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91432419 | ||||||
| chr10:91432453
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.268+7043G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91432453 | ||||||
| chr10:91432668
|
TA | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+7269delA | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 91432668 | |||||
| chr10:91432826
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+7416A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91432826 | ||||||
| chr10:91433203
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+7793G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91433203 | ||||||
| chr10:91433492
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.268+8082A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91433492 | ||||||
| chr10:91433544
|
A | T | 1 | a0001c0001t0001g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.268+8134A>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91433544 | ||||||
| chr10:91433979
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268+8569G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91433979 | ||||||
| chr10:91434233
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.268+8823A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91434233 | ||||||
| chr10:91434628
|
C | CT | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+9225dupT | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 91434628 | |||||
| chr10:91434790
|
C | T | 2 | a0001c0001t0001g0012a0001c0004t0001g0011 | 2 | HG01081.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.268+9380C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91434790 | ||||||
| chr10:91434973
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+9563G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91434973 | ||||||
| chr10:91436326
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+10916G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91436326 | ||||||
| chr10:91437169
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+11759T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91437169 | ||||||
| chr10:91437527
|
T | G | 1 | a0001c0002t0002g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.268+12117T>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91437527 | ||||||
| chr10:91437619
|
CTT | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+12227_268+1222 others(6): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 91437619 | |||||
| chr10:91438090
|
C | CT | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+12691dupT | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 91438090 | |||||
| chr10:91438163
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+12753A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91438163 | ||||||
| chr10:91438314
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+12904C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91438314 | ||||||
| chr10:91438539
|
CAT | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+13130_268+1313 others(6): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91438539 | ||||||
| chr10:91438885
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+13475G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91438885 | ||||||
| chr10:91438942
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+13532A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91438942 | ||||||
| chr10:91439217
|
C | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+13807C>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91439217 | ||||||
| chr10:91439227
|
T | C | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268+13817T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91439227 | ||||||
| chr10:91440180
|
GC | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+14771delC | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91440180 | ||||||
| chr10:91440268
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.268+14858G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91440268 | ||||||
| chr10:91440321
|
G | C | 1 | a0001c0002t0002g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.268+14911G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91440321 | ||||||
| chr10:91440352
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+14942C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91440352 | ||||||
| chr10:91440431
|
T | G | 1 | a0001c0001t0003g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268+15021T>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91440431 | ||||||
| chr10:91440698
|
G | C | 1 | a0001c0002t0002g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.268+15288G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91440698 | ||||||
| chr10:91440782
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.268+15372G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91440782 | ||||||
| chr10:91441906
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0003g0007a0001c0001t0003g0008others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+16496T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91441906 | ||||||
| chr10:91441907
|
T | C | 3 | a0001c0001t0001g0006a0001c0002t0002g0001a0001c0002t0002g0003 | 4 | HG01081.hp1 HG01433.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+16497T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91441907 | ||||||
| chr10:91441907
|
TC | T | 2 | a0001c0001t0004g0013a0001c0002t0002g0002 | 2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.268+16498delC | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91441907 | ||||||
| chr10:91441908
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 10 | HG01081.hp1 HG01433.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.268+16498C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91441908 | ||||||
| chr10:91442287
|
ATC | A | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+16882_268+1688 others(6): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 91442287 | |||||
| chr10:91442534
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.268+17124T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91442534 | ||||||
| chr10:91442595
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.268+17185T>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91442595 | ||||||
| chr10:91442778
|
G | A | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+17368G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91442778 | ||||||
| chr10:91443496
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.269-16931C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91443496 | ||||||
| chr10:91444529
|
C | T | 1 | a0001c0004t0001g0011 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.269-15898C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91444529 | ||||||
| chr10:91444679
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-15748A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91444679 | ||||||
| chr10:91444688
|
A | G | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.269-15739A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91444688 | ||||||
| chr10:91444755
|
TATAA | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-15668_269-1566 others(8): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 91444755 | |||||
| chr10:91445618
|
C | T | 2 | a0001c0002t0002g0001a0001c0002t0002g0003 | 3 | HG01081.hp1 HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.269-14809C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91445618 | ||||||
| chr10:91445809
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.269-14618G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91445809 | ||||||
| chr10:91446121
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.269-14306A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91446121 | ||||||
| chr10:91446839
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0003g0007a0001c0001t0003g0008others(2): Show | 5 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.269-13588C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91446839 | ||||||
| chr10:91447022
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.269-13405A>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91447022 | ||||||
| chr10:91447323
|
TGA | T | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.269-13099_269-1309 others(6): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 91447323 | |||||
| chr10:91447703
|
A | AG | 2 | a0001c0001t0001g0012a0001c0004t0001g0011 | 2 | HG01081.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.269-12724_269-1272 others(5): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91447703 | ||||||
| chr10:91447709
|
A | G | 2 | a0001c0002t0002g0001a0001c0002t0002g0003 | 3 | HG01081.hp1 HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.269-12718A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91447709 | ||||||
| chr10:91447709
|
AG | A | 2 | a0001c0001t0001g0006a0001c0002t0002g0002 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.269-12717delG | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91447709 | ||||||
| chr10:91447710
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0003g0007others(5): Show | 9 | HG01081.hp1 HG01433.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.269-12717G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91447710 | ||||||
| chr10:91447711
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0003g0007others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.269-12716A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91447711 | ||||||
| chr10:91447712
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.269-12715A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91447712 | ||||||
| chr10:91447720
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(9): Show | 13 | HG01081.hp1 HG01081.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.269-12707G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91447720 | ||||||
| chr10:91449176
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-11251A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91449176 | ||||||
| chr10:91449761
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.269-10666G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91449761 | ||||||
| chr10:91449940
|
TG | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-10484delG | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 91449940 | |||||
| chr10:91450077
|
C | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-10350C>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91450077 | ||||||
| chr10:91450156
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-10271A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91450156 | ||||||
| chr10:91450404
|
C | T | 2 | a0001c0001t0001g0012a0001c0004t0001g0011 | 2 | HG01081.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.269-10023C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91450404 | ||||||
| chr10:91450646
|
C | T | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.269-9781C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91450646 | ||||||
| chr10:91450691
|
C | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.269-9736C>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91450691 | ||||||
| chr10:91450817
|
G | T | 1 | a0001c0001t0003g0010 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.269-9610G>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91450817 | ||||||
| chr10:91450968
|
C | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.269-9459C>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91450968 | ||||||
| chr10:91451008
|
T | TGGGG | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.269-9416_269-9415i others(6): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 91451008 | |||||
| chr10:91451130
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.269-9297G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91451130 | ||||||
| chr10:91451446
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.269-8981C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91451446 | ||||||
| chr10:91452489
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-7938C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91452489 | ||||||
| chr10:91453218
|
G | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-7209G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91453218 | ||||||
| chr10:91454064
|
CA | C | 2 | a0001c0002t0002g0001a0001c0002t0002g0003 | 3 | HG01081.hp1 HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.269-6356delA | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr10 | 91454064 | |||||
| chr10:91454525
|
A | G | 2 | a0001c0001t0001g0012a0001c0004t0001g0011 | 2 | HG01081.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.269-5902A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91454525 | ||||||
| chr10:91454711
|
G | T | 2 | a0001c0002t0002g0001a0001c0002t0002g0003 | 3 | HG01081.hp1 HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.269-5716G>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91454711 | ||||||
| chr10:91454790
|
A | C | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.269-5637A>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91454790 | ||||||
| chr10:91454913
|
G | A | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.269-5514G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91454913 | ||||||
| chr10:91455005
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-5422T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91455005 | ||||||
| chr10:91456158
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.269-4269A>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91456158 | ||||||
| chr10:91456354
|
A | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-4073A>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91456354 | ||||||
| chr10:91457095
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.269-3332C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91457095 | ||||||
| chr10:91457300
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-3127T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91457300 | ||||||
| chr10:91457844
|
A | G | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.269-2583A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91457844 | ||||||
| chr10:91457910
|
C | T | 1 | a0001c0002t0002g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.269-2517C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91457910 | ||||||
| chr10:91458015
|
G | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-2412G>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91458015 | ||||||
| chr10:91458037
|
A | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0003g0007others(4): Show | 7 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.269-2390A>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91458037 | ||||||
| chr10:91458780
|
T | C | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.269-1647T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91458780 | ||||||
| chr10:91458854
|
T | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.269-1573T>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91458854 | ||||||
| chr10:91458930
|
G | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.269-1497G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91458930 | ||||||
| chr10:91459489
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-938C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91459489 | ||||||
| chr10:91459764
|
A | C | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.269-663A>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91459764 | ||||||
| chr10:91460347
|
C | T | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.269-80C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 2/20 | chr10 | 91460347 | ||||||
| chr10:91460581
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.407+16T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 3/20 | chr10 | 91460581 | ||||||
| chr10:91461230
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.408-24A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 3/20 | chr10 | 91461230 | ||||||
| chr10:91461843
|
C | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.511-252C>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 4/20 | chr10 | 91461843 | ||||||
| chr10:91462266
|
A | G | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.600+82A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91462266 | ||||||
| chr10:91462807
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+623A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91462807 | ||||||
| chr10:91463068
|
C | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.600+884C>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91463068 | ||||||
| chr10:91463382
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.600+1198G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91463382 | ||||||
| chr10:91465874
|
G | C | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+3690G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91465874 | ||||||
| chr10:91465959
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+3775A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91465959 | ||||||
| chr10:91465964
|
A | G | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.600+3780A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91465964 | ||||||
| chr10:91466793
|
A | G | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.600+4609A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91466793 | ||||||
| chr10:91467981
|
C | T | 1 | a0001c0004t0001g0011 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.600+5797C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91467981 | ||||||
| chr10:91468865
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.600+6681A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91468865 | ||||||
| chr10:91468939
|
C | CA | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(9): Show | 13 | HG01081.hp1 HG01081.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.600+6773dupA | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr10 | 91468939 | |||||
| chr10:91469418
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.600+7234C>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91469418 | ||||||
| chr10:91469970
|
G | T | 1 | a0001c0004t0001g0011 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.600+7786G>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91469970 | ||||||
| chr10:91469991
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.600+7807T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91469991 | ||||||
| chr10:91470758
|
A | G | 1 | a0001c0002t0002g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.601-7443A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91470758 | ||||||
| chr10:91470986
|
A | G | 13 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(10): Show | 14 | HG01081.hp1 HG01081.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.601-7215A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91470986 | ||||||
| chr10:91471012
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.601-7189G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91471012 | ||||||
| chr10:91471540
|
T | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.601-6661T>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91471540 | ||||||
| chr10:91471622
|
A | T | 1 | a0001c0002t0002g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.601-6579A>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91471622 | ||||||
| chr10:91471636
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.601-6565T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91471636 | ||||||
| chr10:91472503
|
A | G | 1 | a0001c0002t0002g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.601-5698A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91472503 | ||||||
| chr10:91474011
|
A | C | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.601-4190A>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91474011 | ||||||
| chr10:91475124
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.601-3077C>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91475124 | ||||||
| chr10:91476105
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.601-2096G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91476105 | ||||||
| chr10:91476115
|
T | C | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.601-2086T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91476115 | ||||||
| chr10:91476242
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.601-1959A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91476242 | ||||||
| chr10:91476506
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.601-1695T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91476506 | ||||||
| chr10:91476582
|
C | T | 1 | a0001c0001t0003g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.601-1619C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91476582 | ||||||
| chr10:91477050
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.601-1151G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91477050 | ||||||
| chr10:91477250
|
T | G | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.601-951T>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 5/20 | chr10 | 91477250 | ||||||
| chr10:91479968
|
T | C | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-1126T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 6/20 | chr10 | 91479968 | ||||||
| chr10:91480409
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.666-685A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 6/20 | chr10 | 91480409 | ||||||
| chr10:91480736
|
T | A | 1 | a0001c0001t0001g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.666-358T>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 6/20 | chr10 | 91480736 | ||||||
| chr10:91480947
|
A | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.666-147A>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 6/20 | chr10 | 91480947 | ||||||
| chr10:91481688
|
C | T | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.711+549C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 7/20 | chr10 | 91481688 | ||||||
| chr10:91482066
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.712-901T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 7/20 | chr10 | 91482066 | ||||||
| chr10:91482429
|
T | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.712-538T>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 7/20 | chr10 | 91482429 | ||||||
| chr10:91482629
|
A | T | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.712-338A>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 7/20 | chr10 | 91482629 | ||||||
| chr10:91482754
|
C | T | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-213C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 7/20 | chr10 | 91482754 | ||||||
| chr10:91483512
|
C | T | 2 | a0001c0002t0002g0001a0001c0002t0002g0003 | 3 | HG01081.hp1 HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.821+436C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 8/20 | chr10 | 91483512 | ||||||
| chr10:91485851
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1094+548T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 10/20 | chr10 | 91485851 | ||||||
| chr10:91486315
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1094+1012T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 10/20 | chr10 | 91486315 | ||||||
| chr10:91486390
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1094+1087G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 10/20 | chr10 | 91486390 | ||||||
| chr10:91486727
|
C | A | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1095-955C>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 10/20 | chr10 | 91486727 | ||||||
| chr10:91486918
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1095-764A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 10/20 | chr10 | 91486918 | ||||||
| chr10:91487103
|
T | TGA | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1095-579_1095-578i others(4): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 10/20 | chr10 | 91487103 | ||||||
| chr10:91487365
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1095-317G>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 10/20 | chr10 | 91487365 | ||||||
| chr10:91488632
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1191+854A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 11/20 | chr10 | 91488632 | ||||||
| chr10:91490232
|
A | AG | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1192-967dupG | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr10 | 91490232 | |||||
| chr10:91490890
|
C | CA | 4 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0003g0007others(1): Show | 4 | HG02486.hp1 HG02486.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192-281dupA | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr10 | 91490890 | |||||
| chr10:91490933
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1192-267C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 11/20 | chr10 | 91490933 | ||||||
| chr10:91491711
|
G | A | 2 | a0001c0002t0002g0001a0001c0002t0002g0003 | 3 | HG01081.hp1 HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1299+404G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 12/20 | chr10 | 91491711 | ||||||
| chr10:91491972
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1300-380A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 12/20 | chr10 | 91491972 | ||||||
| chr10:91492277
|
T | C | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300-75T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 12/20 | chr10 | 91492277 | ||||||
| chr10:91492538
|
G | A | 1 | a0001c0004t0001g0011 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1432+54G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 13/20 | chr10 | 91492538 | ||||||
| chr10:91493796
|
A | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1521+288A>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 14/20 | chr10 | 91493796 | ||||||
| chr10:91493963
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1521+455T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 14/20 | chr10 | 91493963 | ||||||
| chr10:91494027
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1521+519A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 14/20 | chr10 | 91494027 | ||||||
| chr10:91494804
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1521+1296A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 14/20 | chr10 | 91494804 | ||||||
| chr10:91495399
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1522-815T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 14/20 | chr10 | 91495399 | ||||||
| chr10:91495616
|
C | T | 2 | a0001c0002t0002g0001a0001c0002t0002g0003 | 3 | HG01081.hp1 HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1522-598C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 14/20 | chr10 | 91495616 | ||||||
| chr10:91496472
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1680+100G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 15/20 | chr10 | 91496472 | ||||||
| chr10:91497106
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1680+734T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 15/20 | chr10 | 91497106 | ||||||
| chr10:91497126
|
AT | A | 6 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(3): Show | 6 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1680+783delT | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr10 | 91497126 | |||||
| chr10:91497126
|
ATT | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1680+782_1680+783d others(4): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr10 | 91497126 | |||||
| chr10:91497219
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1680+847G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 15/20 | chr10 | 91497219 | ||||||
| chr10:91497315
|
C | CAG | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1681-792_1681-791d others(4): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr10 | 91497315 | |||||
| chr10:91497398
|
C | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1681-710C>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 15/20 | chr10 | 91497398 | ||||||
| chr10:91497456
|
ATT | A | 2 | a0001c0002t0002g0001a0001c0002t0002g0002 | 3 | HG01081.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1681-627_1681-626d others(4): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr10 | 91497456 | |||||
| chr10:91497456
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0003g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1681-636_1681-626d others(13): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr10 | 91497456 | |||||
| chr10:91497456
|
ATTTTTTT others(5): Show |
A | 6 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0003g0008others(3): Show | 6 | HG01081.hp2 HG01433.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1681-637_1681-626d others(14): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr10 | 91497456 | |||||
| chr10:91497456
|
ATTTTTTT others(6): Show |
A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0004g0013 | 3 | HG02486.hp2 HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1681-638_1681-626d others(15): Show |
HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr10 | 91497456 | |||||
| chr10:91497484
|
G | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(10): Show | 14 | HG01081.hp1 HG01081.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1681-624G>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 15/20 | chr10 | 91497484 | ||||||
| chr10:91499508
|
G | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1950+358G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 18/20 | chr10 | 91499508 | ||||||
| chr10:91499710
|
C | G | 1 | a0001c0001t0001g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1950+560C>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 18/20 | chr10 | 91499710 | ||||||
| chr10:91499714
|
A | C | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1950+564A>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 18/20 | chr10 | 91499714 | ||||||
| chr10:91500319
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1951-183G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 18/20 | chr10 | 91500319 | ||||||
| chr10:91500725
|
A | G | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.2066+108A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 19/20 | chr10 | 91500725 | ||||||
| chr10:91501045
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2067-146A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 19/20 | chr10 | 91501045 | ||||||
| chr10:91503335
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2210+2001T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91503335 | ||||||
| chr10:91503628
|
C | T | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2210+2294C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91503628 | ||||||
| chr10:91503648
|
G | T | 2 | a0001c0001t0001g0006a0001c0001t0004g0013 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2210+2314G>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91503648 | ||||||
| chr10:91503768
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2210+2434A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91503768 | ||||||
| chr10:91503948
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2210+2614G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91503948 | ||||||
| chr10:91504596
|
G | A | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.2210+3262G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91504596 | ||||||
| chr10:91504670
|
C | T | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2210+3336C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91504670 | ||||||
| chr10:91504692
|
G | A | 1 | a0001c0002t0002g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2210+3358G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91504692 | ||||||
| chr10:91504707
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2210+3373G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91504707 | ||||||
| chr10:91504742
|
G | A | 1 | a0001c0002t0002g0003 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2210+3408G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91504742 | ||||||
| chr10:91504839
|
G | C | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2210+3505G>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91504839 | ||||||
| chr10:91505140
|
A | C | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.2210+3806A>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91505140 | ||||||
| chr10:91505142
|
C | A | 1 | a0001c0001t0001g0005 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2210+3808C>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91505142 | ||||||
| chr10:91505147
|
G | A | 1 | a0001c0002t0002g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2210+3813G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91505147 | ||||||
| chr10:91505775
|
A | T | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2210+4441A>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91505775 | ||||||
| chr10:91505981
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2210+4647A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91505981 | ||||||
| chr10:91506076
|
G | A | 4 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(1): Show | 4 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.2210+4742G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91506076 | ||||||
| chr10:91506253
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG01081.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2210+4919A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91506253 | ||||||
| chr10:91506651
|
G | A | 1 | a0001c0002t0002g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2210+5317G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91506651 | ||||||
| chr10:91506689
|
A | C | 2 | a0001c0001t0001g0012a0001c0004t0001g0011 | 2 | HG01081.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2210+5355A>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91506689 | ||||||
| chr10:91506698
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2210+5364A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91506698 | ||||||
| chr10:91506891
|
A | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211-5373A>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91506891 | ||||||
| chr10:91506892
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211-5372C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91506892 | ||||||
| chr10:91507486
|
C | A | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2211-4778C>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91507486 | ||||||
| chr10:91507963
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2211-4301T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91507963 | ||||||
| chr10:91508218
|
A | T | 1 | a0001c0001t0003g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2211-4046A>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91508218 | ||||||
| chr10:91508460
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2211-3804G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91508460 | ||||||
| chr10:91508569
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2211-3695A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91508569 | ||||||
| chr10:91508705
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2211-3559G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91508705 | ||||||
| chr10:91508912
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2211-3352G>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91508912 | ||||||
| chr10:91509048
|
C | G | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2211-3216C>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91509048 | ||||||
| chr10:91509122
|
T | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2211-3142T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91509122 | ||||||
| chr10:91509692
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211-2572A>G | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91509692 | ||||||
| chr10:91510215
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2211-2049T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91510215 | ||||||
| chr10:91511827
|
T | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2211-437T>C | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91511827 | ||||||
| chr10:91511950
|
C | T | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2211-314C>T | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91511950 | ||||||
| chr10:91512225
|
T | A | 1 | a0001c0001t0004g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2211-39T>A | HECTD2 | ENSG00000165338.17 | transcript | ENST00000298068.10 | protein_coding | 20/20 | chr10 | 91512225 |