Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79783 |
|---|---|
| ensemblid | ENSG00000175600.16 |
| hgncid | 16001 |
| symbol | SUGCT |
| name | succinyl-CoA:glutarate-CoA transferase |
| refseq_nuc | NM_001193313.2 |
| refseq_prot | NP_001180242.2 |
| ensembl_nuc | ENST00000335693.9 |
| ensembl_prot | ENSP00000338475.5 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 40135005 |
| end | 40860763 |
| strand | + |
| ver | v1.2 |
| region | chr7:40135005-40860763 |
| region5000 | chr7:40130005-40865763 |
| regionname0 | SUGCT_chr7_40135005_40860763 |
| regionname5000 | SUGCT_chr7_40130005_40865763 |
| 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 | 438 | 8 | 2 | 6 | 0 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | copy fasta | chr7 | 40130005 | 40865763 |
| 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 | 1317 | 6 | 1 | 5 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | copy fasta | chr7 | 40130005 | 40865763 |
| c0002 | 0/0 | 1317 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | copy fasta | chr7 | 40130005 | 40865763 |
| c0003 | 0/0 | 1317 | 1 | 1 | 0 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | copy fasta | chr7 | 40130005 | 40865763 |
| 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 | 301 | 8 | 2 | 6 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | copy fasta | chr7 | 40130005 | 40865763 |
| 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 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| 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 | 1317 | 6 | 1 | 5 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | copy fasta | chr7 | 40130005 | 40865763 |
| a0001c0002 | 0/0 | 1317 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | copy fasta | chr7 | 40130005 | 40865763 |
| a0001c0003 | 0/0 | 1317 | 1 | 1 | 0 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | copy fasta | chr7 | 40130005 | 40865763 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1617 | 6 | 1 | 5 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | copy fasta | chr7 | 40130005 | 40865763 |
| a0001c0002t0001 | 0/0 | 1617 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | copy fasta | chr7 | 40130005 | 40865763 |
| a0001c0003t0001 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | copy fasta | chr7 | 40130005 | 40865763 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| a0001c0002t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| a0001c0003t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | ESN | SUGCT_chr7_40130005_40865763 | SUGCT | chr7 | 40130005 | 40865763 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:40274566
|
G | A | 1 | a0001c0002 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.630G>A | p.Leu210Leu | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/14 | 646/1617 | 630/1317 | 210/438 | chr7 | 40274566 | ||
| chr7:40274644
|
A | G | 1 | a0001c0003 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.708A>G | p.Leu236Leu | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/14 | 724/1617 | 708/1317 | 236/438 | chr7 | 40274644 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:40135609
|
T | A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.100+489T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40135609 | ||||||
| chr7:40137153
|
G | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.100+2033G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40137153 | ||||||
| chr7:40137587
|
C | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.100+2467C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40137587 | ||||||
| chr7:40137674
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.100+2554A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40137674 | ||||||
| chr7:40138063
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.100+2943G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40138063 | ||||||
| chr7:40138665
|
AT | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+3553delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 40138665 | |||||
| chr7:40138769
|
T | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.100+3649T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40138769 | ||||||
| chr7:40139127
|
AAAAT | A | 2 | a0001c0001t0001g0003a0001c0002t0001g0001 | 2 | HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.100+4056_100+4059d others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 40139127 | |||||
| chr7:40139127
|
AAAATAAA others(1): Show |
A | 4 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp1 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+4052_100+4059d others(10): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 40139127 | |||||
| chr7:40139168
|
A | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100+4048A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40139168 | ||||||
| chr7:40139172
|
A | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100+4052A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40139172 | ||||||
| chr7:40139176
|
A | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100+4056A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40139176 | ||||||
| chr7:40140014
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.100+4894T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40140014 | ||||||
| chr7:40140534
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.100+5414A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40140534 | ||||||
| chr7:40140849
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.100+5729C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40140849 | ||||||
| chr7:40141436
|
C | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100+6316C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40141436 | ||||||
| chr7:40142377
|
T | A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.100+7257T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40142377 | ||||||
| chr7:40143079
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+7959C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40143079 | ||||||
| chr7:40143080
|
C | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.100+7960C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40143080 | ||||||
| chr7:40143237
|
G | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100+8117G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40143237 | ||||||
| chr7:40144454
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.100+9334G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40144454 | ||||||
| chr7:40144549
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.100+9429T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40144549 | ||||||
| chr7:40144570
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.100+9450C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40144570 | ||||||
| chr7:40144923
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100+9803G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40144923 | ||||||
| chr7:40147055
|
T | TTCTC | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+11939_100+1194 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 40147055 | |||||
| chr7:40148101
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+12981G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40148101 | ||||||
| chr7:40148779
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.100+13659C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40148779 | ||||||
| chr7:40148906
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100+13786C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40148906 | ||||||
| chr7:40148911
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100+13791G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40148911 | ||||||
| chr7:40149182
|
C | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+14062C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40149182 | ||||||
| chr7:40150024
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.100+14904C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40150024 | ||||||
| chr7:40150070
|
G | GC | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+14950_100+1495 others(5): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40150070 | ||||||
| chr7:40150126
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100+15006G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40150126 | ||||||
| chr7:40150803
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+15683T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40150803 | ||||||
| chr7:40150850
|
A | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(3): Show | 6 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+15730A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40150850 | ||||||
| chr7:40150951
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100+15831T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40150951 | ||||||
| chr7:40152846
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.100+17726G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40152846 | ||||||
| chr7:40153104
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100+17984G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40153104 | ||||||
| chr7:40153936
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.100+18816G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40153936 | ||||||
| chr7:40153989
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.100+18869C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40153989 | ||||||
| chr7:40154315
|
G | GAATGT | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.100+19210_100+1921 others(9): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 40154315 | |||||
| chr7:40154349
|
T | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.100+19229T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40154349 | ||||||
| chr7:40154661
|
T | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+19541T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40154661 | ||||||
| chr7:40155949
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.100+20829C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40155949 | ||||||
| chr7:40156845
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+21725G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40156845 | ||||||
| chr7:40157012
|
C | CAA | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.100+21907_100+2190 others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 40157012 | |||||
| chr7:40157346
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+22226C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40157346 | ||||||
| chr7:40157569
|
T | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+22449T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40157569 | ||||||
| chr7:40157900
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.100+22780C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40157900 | ||||||
| chr7:40158611
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.101-22336G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40158611 | ||||||
| chr7:40159473
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.101-21474C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40159473 | ||||||
| chr7:40161154
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.101-19793A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40161154 | ||||||
| chr7:40161368
|
C | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-19579C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40161368 | ||||||
| chr7:40163606
|
GA | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.101-17326delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 40163606 | |||||
| chr7:40163757
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-17190C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40163757 | ||||||
| chr7:40164123
|
G | GA | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.101-16823dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 40164123 | |||||
| chr7:40164125
|
C | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.101-16822C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40164125 | ||||||
| chr7:40164125
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.101-16822C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40164125 | ||||||
| chr7:40165007
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-15940T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40165007 | ||||||
| chr7:40165730
|
AT | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.101-15216delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40165730 | ||||||
| chr7:40166886
|
CA | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(3): Show | 6 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-14044delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 40166886 | |||||
| chr7:40167986
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-12961G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40167986 | ||||||
| chr7:40168227
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.101-12720C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40168227 | ||||||
| chr7:40168579
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.101-12368C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40168579 | ||||||
| chr7:40168846
|
ACT | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-12098_101-1209 others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 40168846 | |||||
| chr7:40169413
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-11534A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40169413 | ||||||
| chr7:40170091
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-10856T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40170091 | ||||||
| chr7:40170145
|
G | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-10802G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40170145 | ||||||
| chr7:40170241
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.101-10706C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40170241 | ||||||
| chr7:40170357
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.101-10590A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40170357 | ||||||
| chr7:40170831
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.101-10116C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40170831 | ||||||
| chr7:40171289
|
G | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-9658G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40171289 | ||||||
| chr7:40172153
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-8794C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40172153 | ||||||
| chr7:40172421
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.101-8526C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40172421 | ||||||
| chr7:40172635
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-8312C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40172635 | ||||||
| chr7:40173556
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.101-7391C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40173556 | ||||||
| chr7:40173714
|
T | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-7233T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40173714 | ||||||
| chr7:40173913
|
CTGTG | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-7002_101-6999d others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 40173913 | |||||
| chr7:40174222
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.101-6725C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40174222 | ||||||
| chr7:40174257
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.101-6690A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40174257 | ||||||
| chr7:40174303
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-6644G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40174303 | ||||||
| chr7:40174889
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-6058T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40174889 | ||||||
| chr7:40175967
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.101-4980C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40175967 | ||||||
| chr7:40175985
|
A | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-4962A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40175985 | ||||||
| chr7:40176084
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-4863C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40176084 | ||||||
| chr7:40176240
|
A | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.101-4707A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40176240 | ||||||
| chr7:40176426
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-4521G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40176426 | ||||||
| chr7:40176702
|
G | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.101-4245G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40176702 | ||||||
| chr7:40176955
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.101-3992C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40176955 | ||||||
| chr7:40176961
|
CAA | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.101-3968_101-3967d others(4): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 40176961 | |||||
| chr7:40177321
|
G | A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.101-3626G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40177321 | ||||||
| chr7:40177925
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-3022A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40177925 | ||||||
| chr7:40178283
|
C | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-2664C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40178283 | ||||||
| chr7:40180813
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-134T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40180813 | ||||||
| chr7:40180908
|
C | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-39C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 1/13 | chr7 | 40180908 | ||||||
| chr7:40181746
|
C | CA | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.153-195dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr7 | 40181746 | |||||
| chr7:40182364
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.226+336C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40182364 | ||||||
| chr7:40182425
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+397A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40182425 | ||||||
| chr7:40183192
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+1164A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40183192 | ||||||
| chr7:40183438
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+1410C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40183438 | ||||||
| chr7:40184132
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.226+2104G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40184132 | ||||||
| chr7:40185367
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.227-3128A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40185367 | ||||||
| chr7:40185530
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-2965C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40185530 | ||||||
| chr7:40185813
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.227-2682A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40185813 | ||||||
| chr7:40186284
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.227-2211G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40186284 | ||||||
| chr7:40187005
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-1490G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40187005 | ||||||
| chr7:40187322
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.227-1173T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40187322 | ||||||
| chr7:40187401
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.227-1094G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40187401 | ||||||
| chr7:40187441
|
A | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.227-1054A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40187441 | ||||||
| chr7:40187708
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.227-787A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40187708 | ||||||
| chr7:40188096
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-399G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40188096 | ||||||
| chr7:40188429
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.227-66A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40188429 | ||||||
| chr7:40188479
|
A | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.227-16A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 3/13 | chr7 | 40188479 | ||||||
| chr7:40188889
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.312+309C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 4/13 | chr7 | 40188889 | ||||||
| chr7:40189115
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-429G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 4/13 | chr7 | 40189115 | ||||||
| chr7:40189291
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-253A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 4/13 | chr7 | 40189291 | ||||||
| chr7:40189299
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-245A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 4/13 | chr7 | 40189299 | ||||||
| chr7:40189398
|
C | CTTTTTTT others(1): Show |
4 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01192.hp1 HG01192.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-139_313-132dup others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 40189398 | |||||
| chr7:40189473
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-71G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 4/13 | chr7 | 40189473 | ||||||
| chr7:40189528
|
A | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.313-16A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 4/13 | chr7 | 40189528 | ||||||
| chr7:40190658
|
A | AT | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1066dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr7 | 40190658 | |||||
| chr7:40190747
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1153T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 5/13 | chr7 | 40190747 | ||||||
| chr7:40192107
|
C | CA | 3 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp1 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.363+2535dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr7 | 40192107 | |||||
| chr7:40192631
|
T | TTTC | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.364-2307_364-2306i others(5): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr7 | 40192631 | |||||
| chr7:40192975
|
T | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.364-1965T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 5/13 | chr7 | 40192975 | ||||||
| chr7:40193012
|
G | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.364-1928G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 5/13 | chr7 | 40193012 | ||||||
| chr7:40193213
|
C | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.364-1727C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 5/13 | chr7 | 40193213 | ||||||
| chr7:40193281
|
T | G | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.364-1659T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 5/13 | chr7 | 40193281 | ||||||
| chr7:40193566
|
G | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.364-1374G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 5/13 | chr7 | 40193566 | ||||||
| chr7:40193576
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1364A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 5/13 | chr7 | 40193576 | ||||||
| chr7:40193603
|
T | A | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.364-1337T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 5/13 | chr7 | 40193603 | ||||||
| chr7:40193668
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1272G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 5/13 | chr7 | 40193668 | ||||||
| chr7:40195143
|
CT | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+96delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 40195143 | |||||
| chr7:40195222
|
CT | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+180delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 40195222 | |||||
| chr7:40195227
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.484+167T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40195227 | ||||||
| chr7:40195324
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.484+264C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40195324 | ||||||
| chr7:40195808
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+748G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40195808 | ||||||
| chr7:40196468
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.484+1408A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40196468 | ||||||
| chr7:40198026
|
A | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+2966A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40198026 | ||||||
| chr7:40198705
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+3645T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40198705 | ||||||
| chr7:40199033
|
C | CTG | 2 | a0001c0001t0001g0008a0001c0003t0001g0005 | 2 | HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.484+3985_484+3986d others(4): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 40199033 | |||||
| chr7:40199550
|
A | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.484+4490A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40199550 | ||||||
| chr7:40199651
|
G | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+4591G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40199651 | ||||||
| chr7:40199675
|
T | A | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.484+4615T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40199675 | ||||||
| chr7:40199792
|
CT | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.484+4746delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 40199792 | |||||
| chr7:40200408
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.484+5348T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40200408 | ||||||
| chr7:40200440
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.484+5380A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40200440 | ||||||
| chr7:40201852
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.484+6792A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40201852 | ||||||
| chr7:40202495
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.484+7435C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40202495 | ||||||
| chr7:40202740
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+7680C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40202740 | ||||||
| chr7:40202790
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.484+7730G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40202790 | ||||||
| chr7:40202938
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+7878A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40202938 | ||||||
| chr7:40205283
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+10223G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40205283 | ||||||
| chr7:40205640
|
CA | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.484+10602delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 40205640 | |||||
| chr7:40206283
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.484+11223C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40206283 | ||||||
| chr7:40206703
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.484+11643A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40206703 | ||||||
| chr7:40206834
|
A | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.484+11774A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40206834 | ||||||
| chr7:40207532
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 7 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.484+12472G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40207532 | ||||||
| chr7:40207603
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.484+12543T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40207603 | ||||||
| chr7:40208195
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.484+13135C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40208195 | ||||||
| chr7:40209084
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.484+14024A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40209084 | ||||||
| chr7:40209448
|
A | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.484+14388A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40209448 | ||||||
| chr7:40209664
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+14604C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40209664 | ||||||
| chr7:40209801
|
A | C | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.484+14741A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40209801 | ||||||
| chr7:40210265
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+15205C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40210265 | ||||||
| chr7:40211667
|
A | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 7 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.484+16607A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40211667 | ||||||
| chr7:40212057
|
C | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.484+16997C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40212057 | ||||||
| chr7:40212333
|
G | A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.484+17273G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40212333 | ||||||
| chr7:40212335
|
G | A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.484+17275G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40212335 | ||||||
| chr7:40212336
|
GATTGCTT others(75): Show |
G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.484+17277_484+1735 others(86): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40212336 | ||||||
| chr7:40212955
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.484+17895G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40212955 | ||||||
| chr7:40213430
|
A | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.484+18370A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40213430 | ||||||
| chr7:40214646
|
T | G | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.484+19586T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40214646 | ||||||
| chr7:40215523
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 7 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.484+20463G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40215523 | ||||||
| chr7:40216319
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.484+21259T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40216319 | ||||||
| chr7:40216455
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.485-21180G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40216455 | ||||||
| chr7:40216726
|
C | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.485-20909C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40216726 | ||||||
| chr7:40217210
|
C | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-20425C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40217210 | ||||||
| chr7:40219433
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.485-18202A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40219433 | ||||||
| chr7:40219890
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.485-17745T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40219890 | ||||||
| chr7:40219954
|
G | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-17681G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40219954 | ||||||
| chr7:40220413
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.485-17222G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40220413 | ||||||
| chr7:40221271
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.485-16364G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40221271 | ||||||
| chr7:40221492
|
G | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.485-16143G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40221492 | ||||||
| chr7:40221572
|
G | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.485-16063G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40221572 | ||||||
| chr7:40222993
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-14642C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40222993 | ||||||
| chr7:40223181
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.485-14454C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40223181 | ||||||
| chr7:40224399
|
CGTGT | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.485-13208_485-1320 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 40224399 | |||||
| chr7:40225290
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.485-12345A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40225290 | ||||||
| chr7:40225911
|
C | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.485-11724C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40225911 | ||||||
| chr7:40227043
|
C | CT | 3 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01192.hp1 HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.485-10571dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 40227043 | |||||
| chr7:40227418
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-10217G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40227418 | ||||||
| chr7:40228130
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.485-9505G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40228130 | ||||||
| chr7:40228512
|
T | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.485-9123T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40228512 | ||||||
| chr7:40228966
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.485-8669C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40228966 | ||||||
| chr7:40229514
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-8121G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40229514 | ||||||
| chr7:40229945
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.485-7690A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40229945 | ||||||
| chr7:40229984
|
G | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.485-7651G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40229984 | ||||||
| chr7:40231021
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-6614C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40231021 | ||||||
| chr7:40231345
|
G | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-6290G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40231345 | ||||||
| chr7:40231534
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.485-6101G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40231534 | ||||||
| chr7:40231625
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-6010A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40231625 | ||||||
| chr7:40231992
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.485-5643T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40231992 | ||||||
| chr7:40232482
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.485-5153A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40232482 | ||||||
| chr7:40232609
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.485-5026T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40232609 | ||||||
| chr7:40232751
|
G | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-4884G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40232751 | ||||||
| chr7:40233345
|
A | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.485-4290A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40233345 | ||||||
| chr7:40235325
|
T | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-2310T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40235325 | ||||||
| chr7:40235332
|
T | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-2303T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40235332 | ||||||
| chr7:40235506
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-2129C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40235506 | ||||||
| chr7:40235836
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-1799T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40235836 | ||||||
| chr7:40236442
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.485-1187_485-1176d others(14): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 40236442 | |||||
| chr7:40236442
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.485-1188_485-1176d others(15): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 40236442 | |||||
| chr7:40236442
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0007 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.485-1189_485-1176d others(16): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 40236442 | |||||
| chr7:40236442
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0008 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.485-1190_485-1176d others(17): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 40236442 | |||||
| chr7:40236460
|
T | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.485-1175T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40236460 | ||||||
| chr7:40237629
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
splice_region_variant&intron_variant | LOW | c.485-6T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 6/13 | chr7 | 40237629 | ||||||
| chr7:40238439
|
T | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+713T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40238439 | ||||||
| chr7:40238652
|
TATTA | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+939_576+942del others(4): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40238652 | |||||
| chr7:40238822
|
CT | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp1 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+1112delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40238822 | |||||
| chr7:40239311
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+1585A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40239311 | ||||||
| chr7:40239663
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+1937T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40239663 | ||||||
| chr7:40241919
|
C | CA | 5 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG00738.hp1 HG01069.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.576+4209dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40241919 | |||||
| chr7:40242931
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.576+5205A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40242931 | ||||||
| chr7:40242933
|
A | ATATATAT others(17): Show |
1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.576+5208_576+5209i others(26): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40242933 | |||||
| chr7:40242933
|
A | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0006 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.576+5207A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40242933 | ||||||
| chr7:40244220
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+6494A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40244220 | ||||||
| chr7:40244567
|
T | G | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+6841T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40244567 | ||||||
| chr7:40244870
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+7144T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40244870 | ||||||
| chr7:40245404
|
C | CATATATA others(9): Show |
1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.576+7683_576+7698d others(18): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40245404 | |||||
| chr7:40245421
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.576+7695A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245421 | ||||||
| chr7:40245423
|
A | ATATATAT others(32): Show |
1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.576+7698_576+7699i others(41): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40245423 | |||||
| chr7:40245423
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.576+7697A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245423 | ||||||
| chr7:40245425
|
T | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0007 | 2 | HG01069.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.576+7699T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245425 | ||||||
| chr7:40245426
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(1): Show | 4 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+7700T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245426 | ||||||
| chr7:40245427
|
T | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0007 | 2 | HG01069.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.576+7701T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245427 | ||||||
| chr7:40245429
|
T | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.576+7703T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245429 | ||||||
| chr7:40245431
|
T | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.576+7705T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245431 | ||||||
| chr7:40245433
|
T | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.576+7707T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245433 | ||||||
| chr7:40245434
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.576+7708T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245434 | ||||||
| chr7:40245442
|
T | A | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+7716T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245442 | ||||||
| chr7:40245450
|
T | A | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+7724T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245450 | ||||||
| chr7:40245532
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.576+7806C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245532 | ||||||
| chr7:40245660
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.576+7934G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245660 | ||||||
| chr7:40245681
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+7955A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40245681 | ||||||
| chr7:40246251
|
C | CT | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+8537dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40246251 | |||||
| chr7:40246285
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.576+8559T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40246285 | ||||||
| chr7:40246297
|
T | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.576+8571T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40246297 | ||||||
| chr7:40246599
|
CT | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+8888delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40246599 | |||||
| chr7:40247019
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.576+9293T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40247019 | ||||||
| chr7:40247152
|
G | A | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+9426G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40247152 | ||||||
| chr7:40247505
|
G | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+9779G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40247505 | ||||||
| chr7:40247598
|
C | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+9872C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40247598 | ||||||
| chr7:40247603
|
G | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+9877G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40247603 | ||||||
| chr7:40247876
|
TAA | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.576+10151_576+1015 others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40247876 | ||||||
| chr7:40247879
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.576+10153G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40247879 | ||||||
| chr7:40247906
|
T | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.576+10180T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40247906 | ||||||
| chr7:40248002
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+10276T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40248002 | ||||||
| chr7:40248005
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.576+10279G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40248005 | ||||||
| chr7:40248013
|
GT | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+10302delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40248013 | |||||
| chr7:40248262
|
G | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.576+10536G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40248262 | ||||||
| chr7:40248785
|
C | T | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+11059C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40248785 | ||||||
| chr7:40248884
|
G | A | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+11158G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40248884 | ||||||
| chr7:40248888
|
G | GCACACAC others(1): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.576+11176_576+1118 others(12): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40248888 | |||||
| chr7:40248890
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.576+11164A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40248890 | ||||||
| chr7:40248910
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.576+11184G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40248910 | ||||||
| chr7:40248926
|
T | A | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+11200T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40248926 | ||||||
| chr7:40248928
|
C | A | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+11202C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40248928 | ||||||
| chr7:40248932
|
T | C | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+11206T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40248932 | ||||||
| chr7:40249313
|
C | CTATATAT others(5): Show |
2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01069.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.576+11610_576+1162 others(16): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40249313 | |||||
| chr7:40249313
|
C | CTATATAT others(11): Show |
1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.576+11604_576+1162 others(22): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40249313 | |||||
| chr7:40249313
|
C | CTATATAT others(15): Show |
1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.576+11600_576+1162 others(26): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40249313 | |||||
| chr7:40249313
|
C | CTATCTAT others(19): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.576+11590_576+1159 others(30): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40249313 | |||||
| chr7:40249563
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+11837A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40249563 | ||||||
| chr7:40250265
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.576+12539A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40250265 | ||||||
| chr7:40250828
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.576+13116_576+1312 others(17): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40250828 | |||||
| chr7:40250833
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.576+13107T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40250833 | ||||||
| chr7:40250834
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.576+13108T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40250834 | ||||||
| chr7:40250915
|
C | T | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+13189C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40250915 | ||||||
| chr7:40251092
|
C | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+13366C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40251092 | ||||||
| chr7:40251380
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.576+13654T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40251380 | ||||||
| chr7:40251384
|
A | C | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.576+13658A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40251384 | ||||||
| chr7:40251471
|
C | T | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+13745C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40251471 | ||||||
| chr7:40251894
|
CTTCGG | C | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+14171_576+1417 others(9): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40251894 | |||||
| chr7:40252215
|
G | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp2 HG01192.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+14489G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40252215 | ||||||
| chr7:40252626
|
A | G | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.576+14900A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40252626 | ||||||
| chr7:40253026
|
A | G | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+15300A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40253026 | ||||||
| chr7:40253388
|
A | G | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+15662A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40253388 | ||||||
| chr7:40253492
|
C | T | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+15766C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40253492 | ||||||
| chr7:40253717
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.576+15991C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40253717 | ||||||
| chr7:40253897
|
G | A | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.576+16171G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40253897 | ||||||
| chr7:40254473
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.576+16747C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40254473 | ||||||
| chr7:40254551
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp2 HG01192.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+16825A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40254551 | ||||||
| chr7:40254836
|
A | T | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+17110A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40254836 | ||||||
| chr7:40255660
|
C | CA | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+17961dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40255660 | |||||
| chr7:40255736
|
T | A | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+18010T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40255736 | ||||||
| chr7:40255931
|
A | G | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+18205A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40255931 | ||||||
| chr7:40256838
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.577-17675G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40256838 | ||||||
| chr7:40257732
|
G | A | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.577-16781G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40257732 | ||||||
| chr7:40257761
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.577-16752C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40257761 | ||||||
| chr7:40257813
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.577-16700G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40257813 | ||||||
| chr7:40258612
|
C | T | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.577-15901C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40258612 | ||||||
| chr7:40259213
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-15300A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40259213 | ||||||
| chr7:40259279
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp2 HG01192.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-15234G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40259279 | ||||||
| chr7:40259772
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-14741T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40259772 | ||||||
| chr7:40260512
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.577-14001C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40260512 | ||||||
| chr7:40262481
|
C | T | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.577-12032C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40262481 | ||||||
| chr7:40262495
|
C | CA | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.577-11998dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40262495 | |||||
| chr7:40262495
|
CA | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.577-11998delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40262495 | |||||
| chr7:40262620
|
G | A | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.577-11893G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40262620 | ||||||
| chr7:40262644
|
G | A | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.577-11869G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40262644 | ||||||
| chr7:40262918
|
A | G | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.577-11595A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40262918 | ||||||
| chr7:40263024
|
A | G | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.577-11489A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40263024 | ||||||
| chr7:40263274
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.577-11239A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40263274 | ||||||
| chr7:40263685
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-10828G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40263685 | ||||||
| chr7:40263812
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-10701A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40263812 | ||||||
| chr7:40265463
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.577-9050C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40265463 | ||||||
| chr7:40265513
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-9000G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40265513 | ||||||
| chr7:40265907
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.577-8606C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40265907 | ||||||
| chr7:40265959
|
C | CCA | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.577-8537_577-8536d others(4): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40265959 | |||||
| chr7:40266185
|
C | CTT | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-8313_577-8312d others(4): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40266185 | |||||
| chr7:40266218
|
C | T | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.577-8295C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40266218 | ||||||
| chr7:40266570
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-7943A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40266570 | ||||||
| chr7:40266872
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-7641G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40266872 | ||||||
| chr7:40267025
|
A | AAAAC | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-7476_577-7473d others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40267025 | |||||
| chr7:40267424
|
T | C | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.577-7089T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40267424 | ||||||
| chr7:40267579
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.577-6934T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40267579 | ||||||
| chr7:40268653
|
A | AT | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-5848dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40268653 | |||||
| chr7:40268802
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.577-5711T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40268802 | ||||||
| chr7:40268883
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.577-5630C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40268883 | ||||||
| chr7:40269085
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.577-5428A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40269085 | ||||||
| chr7:40269732
|
G | A | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.577-4781G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40269732 | ||||||
| chr7:40269803
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.577-4710T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40269803 | ||||||
| chr7:40270097
|
T | C | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.577-4416T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40270097 | ||||||
| chr7:40270895
|
GT | G | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.577-3617delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40270895 | ||||||
| chr7:40271102
|
A | C | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.577-3411A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40271102 | ||||||
| chr7:40271361
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.577-3152G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40271361 | ||||||
| chr7:40271783
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-2730C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40271783 | ||||||
| chr7:40271816
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.577-2697C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40271816 | ||||||
| chr7:40271978
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-2535A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40271978 | ||||||
| chr7:40272068
|
GCTCTCTC others(3): Show |
G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.577-2426_577-2417d others(12): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40272068 | |||||
| chr7:40272097
|
A | C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.577-2416A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40272097 | ||||||
| chr7:40272113
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-2400G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40272113 | ||||||
| chr7:40272141
|
C | CATATAT | 2 | a0001c0001t0001g0007a0001c0003t0001g0005 | 2 | HG01069.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.577-2324_577-2319d others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40272141 | |||||
| chr7:40272141
|
CATATATA others(11): Show |
C | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.577-2336_577-2319d others(20): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40272141 | |||||
| chr7:40272141
|
CATATATA others(15): Show |
C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.577-2340_577-2319d others(24): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40272141 | |||||
| chr7:40272141
|
CATATATA others(31): Show |
C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.577-2356_577-2319d others(40): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40272141 | |||||
| chr7:40272191
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.577-2322T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40272191 | ||||||
| chr7:40272193
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.577-2320T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40272193 | ||||||
| chr7:40272606
|
A | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.577-1907A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40272606 | ||||||
| chr7:40272661
|
A | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.577-1852A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40272661 | ||||||
| chr7:40272664
|
A | T | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.577-1849A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40272664 | ||||||
| chr7:40272667
|
T | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-1846T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40272667 | ||||||
| chr7:40272895
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.577-1618G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40272895 | ||||||
| chr7:40272899
|
A | AT | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.577-1613dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40272899 | |||||
| chr7:40273249
|
C | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-1264C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40273249 | ||||||
| chr7:40273710
|
T | C | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.577-803T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40273710 | ||||||
| chr7:40274036
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-477T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40274036 | ||||||
| chr7:40274073
|
C | CTTTT | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.577-418_577-415dup others(4): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 40274073 | |||||
| chr7:40276817
|
GTGTC | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.720+2177_720+2180d others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40276817 | |||||
| chr7:40277013
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.720+2357G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40277013 | ||||||
| chr7:40277268
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+2612T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40277268 | ||||||
| chr7:40277316
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.720+2660G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40277316 | ||||||
| chr7:40277348
|
A | ATT | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+2703_720+2704d others(4): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40277348 | |||||
| chr7:40277386
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+2730T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40277386 | ||||||
| chr7:40277677
|
G | GTTATTA | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.720+3044_720+3049d others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40277677 | |||||
| chr7:40277677
|
G | GTTATTAT others(5): Show |
1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.720+3038_720+3049d others(14): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40277677 | |||||
| chr7:40277987
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+3331C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40277987 | ||||||
| chr7:40278005
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+3349G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40278005 | ||||||
| chr7:40278385
|
A | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.720+3729A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40278385 | ||||||
| chr7:40278503
|
A | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.720+3847A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40278503 | ||||||
| chr7:40278589
|
T | G | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.720+3933T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40278589 | ||||||
| chr7:40278841
|
T | TA | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+4188dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40278841 | |||||
| chr7:40279022
|
T | TG | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+4373dupG | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40279022 | |||||
| chr7:40279112
|
C | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.720+4456C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40279112 | ||||||
| chr7:40279368
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+4712C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40279368 | ||||||
| chr7:40279640
|
TAAC | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.720+4986_720+4988d others(5): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40279640 | |||||
| chr7:40279773
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+5117C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40279773 | ||||||
| chr7:40279927
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.720+5271G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40279927 | ||||||
| chr7:40280023
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+5367C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40280023 | ||||||
| chr7:40280296
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.720+5640A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40280296 | ||||||
| chr7:40280518
|
C | A | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.720+5862C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40280518 | ||||||
| chr7:40280894
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+6238C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40280894 | ||||||
| chr7:40281148
|
G | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+6492G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40281148 | ||||||
| chr7:40281236
|
GC | G | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.720+6583delC | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40281236 | |||||
| chr7:40281630
|
G | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+6974G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40281630 | ||||||
| chr7:40281758
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+7102G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40281758 | ||||||
| chr7:40281918
|
G | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+7262G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40281918 | ||||||
| chr7:40282492
|
AAAAC | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+7860_720+7863d others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40282492 | |||||
| chr7:40282684
|
C | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+8028C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40282684 | ||||||
| chr7:40283145
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+8489G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40283145 | ||||||
| chr7:40283414
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+8758C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40283414 | ||||||
| chr7:40283418
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.720+8762G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40283418 | ||||||
| chr7:40284289
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.720+9633T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40284289 | ||||||
| chr7:40284445
|
T | C | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.720+9789T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40284445 | ||||||
| chr7:40284746
|
A | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.720+10090A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40284746 | ||||||
| chr7:40285491
|
T | TG | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.720+10835_720+1083 others(5): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40285491 | ||||||
| chr7:40285491
|
TC | T | 2 | a0001c0001t0001g0006a0001c0002t0001g0001 | 2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.720+10836delC | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40285491 | ||||||
| chr7:40285492
|
C | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+10836C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40285492 | ||||||
| chr7:40285499
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.720+10843G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40285499 | ||||||
| chr7:40286069
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+11413G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40286069 | ||||||
| chr7:40286332
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+11676C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40286332 | ||||||
| chr7:40286424
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.720+11768G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40286424 | ||||||
| chr7:40286824
|
T | TTTTG | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+12181_720+1218 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40286824 | |||||
| chr7:40287489
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+12833C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40287489 | ||||||
| chr7:40287500
|
C | CT | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004 | 3 | HG00738.hp1 HG01069.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.720+12858dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40287500 | |||||
| chr7:40287837
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+13181T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40287837 | ||||||
| chr7:40288316
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+13660G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40288316 | ||||||
| chr7:40288520
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.720+13864C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40288520 | ||||||
| chr7:40288717
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.720+14061A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40288717 | ||||||
| chr7:40288990
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.720+14334C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40288990 | ||||||
| chr7:40290034
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+15378C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40290034 | ||||||
| chr7:40290572
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+15916T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40290572 | ||||||
| chr7:40290735
|
A | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.720+16079A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40290735 | ||||||
| chr7:40290824
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+16168T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40290824 | ||||||
| chr7:40290941
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+16285C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40290941 | ||||||
| chr7:40291008
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+16352A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40291008 | ||||||
| chr7:40291032
|
T | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004 | 3 | HG00738.hp1 HG01069.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.720+16376T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40291032 | ||||||
| chr7:40291097
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+16441T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40291097 | ||||||
| chr7:40291219
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.720+16563G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40291219 | ||||||
| chr7:40291353
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+16697C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40291353 | ||||||
| chr7:40291388
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.720+16732A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40291388 | ||||||
| chr7:40291390
|
C | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.720+16734C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40291390 | ||||||
| chr7:40291398
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+16742T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40291398 | ||||||
| chr7:40291672
|
A | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.720+17016A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40291672 | ||||||
| chr7:40291736
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.720+17080A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40291736 | ||||||
| chr7:40292919
|
A | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.720+18263A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40292919 | ||||||
| chr7:40293482
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+18826A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40293482 | ||||||
| chr7:40293986
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+19330T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40293986 | ||||||
| chr7:40294343
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.720+19687T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40294343 | ||||||
| chr7:40294495
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.720+19839A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40294495 | ||||||
| chr7:40295445
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.720+20789G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40295445 | ||||||
| chr7:40295594
|
C | CAAAT | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+20942_720+2094 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40295594 | |||||
| chr7:40295756
|
G | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.721-21004G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40295756 | ||||||
| chr7:40296143
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.721-20617A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40296143 | ||||||
| chr7:40296483
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-20277A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40296483 | ||||||
| chr7:40296612
|
CGTGTGTG others(3): Show |
C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.721-20115_721-2010 others(14): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40296612 | |||||
| chr7:40296612
|
CGTGTGTG others(13): Show |
C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-20125_721-2010 others(24): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40296612 | |||||
| chr7:40297339
|
T | A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.721-19421T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40297339 | ||||||
| chr7:40297510
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.721-19250G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40297510 | ||||||
| chr7:40297590
|
C | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.721-19170C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40297590 | ||||||
| chr7:40298547
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.721-18213T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40298547 | ||||||
| chr7:40298772
|
C | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.721-17988C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40298772 | ||||||
| chr7:40298954
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.721-17806C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40298954 | ||||||
| chr7:40299648
|
C | CA | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-17101dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40299648 | |||||
| chr7:40299792
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.721-16968C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40299792 | ||||||
| chr7:40300549
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.721-16211T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40300549 | ||||||
| chr7:40300587
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.721-16173A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40300587 | ||||||
| chr7:40300912
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-15848G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40300912 | ||||||
| chr7:40301030
|
A | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.721-15730A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40301030 | ||||||
| chr7:40301745
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.721-15015C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40301745 | ||||||
| chr7:40302289
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.721-14471C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40302289 | ||||||
| chr7:40302351
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.721-14409T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40302351 | ||||||
| chr7:40302419
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.721-14341A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40302419 | ||||||
| chr7:40302922
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.721-13838C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40302922 | ||||||
| chr7:40303263
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.721-13497A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40303263 | ||||||
| chr7:40303892
|
G | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.721-12868G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40303892 | ||||||
| chr7:40304759
|
AATC | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-11997_721-1199 others(7): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40304759 | |||||
| chr7:40305183
|
C | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.721-11577C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40305183 | ||||||
| chr7:40305974
|
AT | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.721-10782delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40305974 | |||||
| chr7:40305983
|
T | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-10777T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40305983 | ||||||
| chr7:40306055
|
C | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-10705C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40306055 | ||||||
| chr7:40306685
|
A | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.721-10075A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40306685 | ||||||
| chr7:40307001
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.721-9759T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40307001 | ||||||
| chr7:40307070
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-9690A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40307070 | ||||||
| chr7:40307423
|
G | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.721-9337G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40307423 | ||||||
| chr7:40307432
|
T | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.721-9328T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40307432 | ||||||
| chr7:40307815
|
A | AT | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-8945_721-8944i others(3): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40307815 | ||||||
| chr7:40308500
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-8260A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40308500 | ||||||
| chr7:40308638
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.721-8122G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40308638 | ||||||
| chr7:40309300
|
G | GT | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-7450dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40309300 | |||||
| chr7:40309789
|
C | CGATGTGT others(11): Show |
4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-6969_721-6968i others(20): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40309789 | |||||
| chr7:40309892
|
TAA | T | 3 | a0001c0001t0001g0006a0001c0002t0001g0001a0001c0003t0001g0005 | 3 | HG00738.hp2 HG01192.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.721-6854_721-6853d others(4): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40309892 | |||||
| chr7:40309892
|
TAAA | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.721-6855_721-6853d others(5): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40309892 | |||||
| chr7:40310106
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.721-6654T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40310106 | ||||||
| chr7:40310142
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.721-6618C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40310142 | ||||||
| chr7:40310190
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.721-6570A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40310190 | ||||||
| chr7:40310396
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.721-6364C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40310396 | ||||||
| chr7:40311288
|
A | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.721-5472A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40311288 | ||||||
| chr7:40311327
|
T | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.721-5433T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40311327 | ||||||
| chr7:40311476
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-5284A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40311476 | ||||||
| chr7:40311624
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.721-5136C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40311624 | ||||||
| chr7:40312050
|
G | GTT | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-4697_721-4696d others(4): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40312050 | |||||
| chr7:40312165
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-4595G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40312165 | ||||||
| chr7:40312268
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-4492C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40312268 | ||||||
| chr7:40312316
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-4444C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40312316 | ||||||
| chr7:40312460
|
TA | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-4299delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40312460 | ||||||
| chr7:40312473
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.721-4287G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40312473 | ||||||
| chr7:40312593
|
A | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.721-4167A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40312593 | ||||||
| chr7:40312644
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-4116A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40312644 | ||||||
| chr7:40312858
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-3902G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40312858 | ||||||
| chr7:40312952
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.721-3808C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40312952 | ||||||
| chr7:40313003
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.721-3757T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40313003 | ||||||
| chr7:40313632
|
TTTTTG | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-3123_721-3119d others(7): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40313632 | |||||
| chr7:40313659
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.721-3101A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40313659 | ||||||
| chr7:40313884
|
T | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.721-2876T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40313884 | ||||||
| chr7:40314114
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-2646T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40314114 | ||||||
| chr7:40314559
|
C | CTTTTT | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0003t0001g0005 | 3 | HG00738.hp2 HG01069.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.721-2183_721-2179d others(7): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40314559 | |||||
| chr7:40314607
|
G | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-2153G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40314607 | ||||||
| chr7:40314773
|
AGGCT | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-1984_721-1981d others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40314773 | |||||
| chr7:40315112
|
TA | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-1640delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 40315112 | |||||
| chr7:40315164
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-1596A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40315164 | ||||||
| chr7:40315433
|
C | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-1327C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40315433 | ||||||
| chr7:40315462
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.721-1298C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40315462 | ||||||
| chr7:40315546
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.721-1214T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40315546 | ||||||
| chr7:40315735
|
T | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-1025T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40315735 | ||||||
| chr7:40315760
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.721-1000G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40315760 | ||||||
| chr7:40315882
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-878T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40315882 | ||||||
| chr7:40315954
|
C | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.721-806C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40315954 | ||||||
| chr7:40316555
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.721-205T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40316555 | ||||||
| chr7:40316716
|
A | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-44A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40316716 | ||||||
| chr7:40317118
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+263G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40317118 | ||||||
| chr7:40317125
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+270G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40317125 | ||||||
| chr7:40317142
|
TTC | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+288_816+289del others(2): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40317142 | ||||||
| chr7:40317237
|
C | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.816+382C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40317237 | ||||||
| chr7:40318375
|
C | CAG | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+1522_816+1523d others(4): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40318375 | |||||
| chr7:40318541
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+1686G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40318541 | ||||||
| chr7:40318834
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+1979T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40318834 | ||||||
| chr7:40318886
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+2031A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40318886 | ||||||
| chr7:40319097
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+2242A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40319097 | ||||||
| chr7:40319191
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+2336A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40319191 | ||||||
| chr7:40319595
|
T | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+2740T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40319595 | ||||||
| chr7:40319900
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.816+3045G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40319900 | ||||||
| chr7:40319965
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+3110G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40319965 | ||||||
| chr7:40319969
|
C | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+3114C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40319969 | ||||||
| chr7:40320112
|
TTG | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+3259_816+3260d others(4): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40320112 | |||||
| chr7:40320140
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+3285T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40320140 | ||||||
| chr7:40320223
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+3368C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40320223 | ||||||
| chr7:40320255
|
A | AG | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+3400_816+3401i others(3): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40320255 | ||||||
| chr7:40320262
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+3407C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40320262 | ||||||
| chr7:40320271
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+3416G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40320271 | ||||||
| chr7:40320357
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+3502C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40320357 | ||||||
| chr7:40320385
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+3530C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40320385 | ||||||
| chr7:40320658
|
T | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+3803T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40320658 | ||||||
| chr7:40320767
|
GA | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+3919delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40320767 | |||||
| chr7:40320851
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0003t0001g0005 | 3 | HG00738.hp2 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.816+3996T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40320851 | ||||||
| chr7:40320903
|
G | A | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.816+4048G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40320903 | ||||||
| chr7:40321101
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.816+4246G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40321101 | ||||||
| chr7:40321132
|
A | AG | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(1): Show | 4 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+4277_816+4278i others(3): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40321132 | ||||||
| chr7:40321152
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.816+4297T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40321152 | ||||||
| chr7:40321222
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+4367A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40321222 | ||||||
| chr7:40321591
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.816+4736C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40321591 | ||||||
| chr7:40322235
|
G | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+5380G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40322235 | ||||||
| chr7:40322697
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+5842C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40322697 | ||||||
| chr7:40322973
|
T | TAAATAAA others(3): Show |
1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.816+6131_816+6140d others(12): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40322973 | |||||
| chr7:40322973
|
T | TAAATAAA others(13): Show |
1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.816+6121_816+6140d others(22): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40322973 | |||||
| chr7:40322973
|
T | TAAATAAA others(18): Show |
2 | a0001c0001t0001g0004a0001c0003t0001g0005 | 2 | HG00738.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.816+6140_816+6141i others(27): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40322973 | |||||
| chr7:40323135
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+6280C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40323135 | ||||||
| chr7:40323551
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+6696C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40323551 | ||||||
| chr7:40324096
|
A | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.816+7241A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324096 | ||||||
| chr7:40324136
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+7281C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324136 | ||||||
| chr7:40324232
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+7377T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324232 | ||||||
| chr7:40324240
|
A | AATATATA others(17): Show |
1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+7388_816+7389i others(26): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40324240 | |||||
| chr7:40324244
|
A | T | 3 | a0001c0001t0001g0003a0001c0002t0001g0001a0001c0003t0001g0005 | 3 | HG01069.hp1 HG01192.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.816+7389A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324244 | ||||||
| chr7:40324248
|
A | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+7393A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324248 | ||||||
| chr7:40324252
|
A | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+7397A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324252 | ||||||
| chr7:40324261
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.816+7409_816+7410i others(22): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40324261 | |||||
| chr7:40324261
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.816+7409_816+7410i others(24): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40324261 | |||||
| chr7:40324261
|
A | ATATATAT others(13): Show |
1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.816+7409_816+7410i others(22): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40324261 | |||||
| chr7:40324400
|
T | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+7545T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324400 | ||||||
| chr7:40324401
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+7546A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324401 | ||||||
| chr7:40324412
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+7557T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324412 | ||||||
| chr7:40324546
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+7691A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324546 | ||||||
| chr7:40324717
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+7862A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324717 | ||||||
| chr7:40324826
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+7971T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324826 | ||||||
| chr7:40324849
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+7994A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324849 | ||||||
| chr7:40324989
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+8134A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40324989 | ||||||
| chr7:40325010
|
G | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+8155G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40325010 | ||||||
| chr7:40325127
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+8272A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40325127 | ||||||
| chr7:40325232
|
A | AT | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+8386dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40325232 | |||||
| chr7:40325242
|
A | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+8387A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40325242 | ||||||
| chr7:40325898
|
C | CTTT | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+9051_816+9053d others(5): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40325898 | |||||
| chr7:40325909
|
G | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+9054G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40325909 | ||||||
| chr7:40325913
|
G | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+9058G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40325913 | ||||||
| chr7:40326920
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+10065A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40326920 | ||||||
| chr7:40327087
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+10232T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40327087 | ||||||
| chr7:40327276
|
TA | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+10424delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40327276 | |||||
| chr7:40327279
|
A | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+10424A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40327279 | ||||||
| chr7:40327291
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+10436T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40327291 | ||||||
| chr7:40327982
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+11127T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40327982 | ||||||
| chr7:40328298
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+11443T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40328298 | ||||||
| chr7:40328350
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+11495T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40328350 | ||||||
| chr7:40328697
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+11842A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40328697 | ||||||
| chr7:40329283
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+12428T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40329283 | ||||||
| chr7:40330482
|
A | AT | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+13638dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40330482 | |||||
| chr7:40330690
|
CATTT | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+13841_816+1384 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40330690 | |||||
| chr7:40330806
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+13951C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40330806 | ||||||
| chr7:40331603
|
C | CTGT | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+14749_816+1475 others(7): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40331603 | |||||
| chr7:40331605
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+14750A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40331605 | ||||||
| chr7:40332272
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+15417G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40332272 | ||||||
| chr7:40332443
|
AT | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+15599delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40332443 | |||||
| chr7:40332455
|
G | T | 1 | a0001c0001t0001g0007 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.816+15600G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40332455 | ||||||
| chr7:40332994
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+16139C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40332994 | ||||||
| chr7:40333359
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+16504G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40333359 | ||||||
| chr7:40333656
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.816+16803_816+1681 others(18): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40333656 | |||||
| chr7:40333657
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.816+16804_816+1682 others(21): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40333657 | |||||
| chr7:40333660
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.816+16807_816+1682 others(20): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40333660 | |||||
| chr7:40333661
|
AAAAAAAA others(14): Show |
A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+16808_816+1682 others(25): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40333661 | |||||
| chr7:40333668
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+16813A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40333668 | ||||||
| chr7:40333704
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+16849A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40333704 | ||||||
| chr7:40333760
|
C | CT | 3 | a0001c0001t0001g0004a0001c0002t0001g0001a0001c0003t0001g0005 | 3 | HG00738.hp1 HG01192.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.816+16914dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40333760 | |||||
| chr7:40333931
|
G | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+17076G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40333931 | ||||||
| chr7:40334856
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+18001G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40334856 | ||||||
| chr7:40334894
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+18039T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40334894 | ||||||
| chr7:40334979
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+18124G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40334979 | ||||||
| chr7:40335312
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+18457G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40335312 | ||||||
| chr7:40335355
|
C | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+18500C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40335355 | ||||||
| chr7:40335407
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+18552A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40335407 | ||||||
| chr7:40335503
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+18648T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40335503 | ||||||
| chr7:40335622
|
A | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.816+18767A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40335622 | ||||||
| chr7:40335646
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+18791G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40335646 | ||||||
| chr7:40336062
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+19207A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40336062 | ||||||
| chr7:40336166
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+19311A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40336166 | ||||||
| chr7:40336693
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+19838A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40336693 | ||||||
| chr7:40337865
|
A | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+21010A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40337865 | ||||||
| chr7:40338084
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+21229T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40338084 | ||||||
| chr7:40338746
|
C | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+21891C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40338746 | ||||||
| chr7:40338749
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.816+21894G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40338749 | ||||||
| chr7:40338973
|
T | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+22118T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40338973 | ||||||
| chr7:40339052
|
C | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.816+22197C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40339052 | ||||||
| chr7:40339368
|
C | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+22513C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40339368 | ||||||
| chr7:40339449
|
G | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+22594G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40339449 | ||||||
| chr7:40339474
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+22619A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40339474 | ||||||
| chr7:40339995
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+23140T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40339995 | ||||||
| chr7:40341432
|
A | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+24577A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40341432 | ||||||
| chr7:40341941
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+25086A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40341941 | ||||||
| chr7:40342647
|
CT | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+25805delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40342647 | |||||
| chr7:40343282
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+26427A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40343282 | ||||||
| chr7:40343549
|
T | TC | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+26696dupC | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40343549 | |||||
| chr7:40343560
|
A | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+26705A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40343560 | ||||||
| chr7:40344337
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+27482T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40344337 | ||||||
| chr7:40344431
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+27576C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40344431 | ||||||
| chr7:40344895
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+28040G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40344895 | ||||||
| chr7:40344976
|
A | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+28121A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40344976 | ||||||
| chr7:40346573
|
C | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+29718C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40346573 | ||||||
| chr7:40346718
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+29863G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40346718 | ||||||
| chr7:40346745
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+29890G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40346745 | ||||||
| chr7:40347236
|
A | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+30381A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40347236 | ||||||
| chr7:40347860
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+31005T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40347860 | ||||||
| chr7:40349096
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+32241G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40349096 | ||||||
| chr7:40350277
|
CTTAT | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp1 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+33473_816+3347 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40350277 | |||||
| chr7:40350277
|
CTTATTTA others(1): Show |
C | 2 | a0001c0001t0001g0006a0001c0003t0001g0005 | 2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.816+33469_816+3347 others(12): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40350277 | |||||
| chr7:40350492
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+33637T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40350492 | ||||||
| chr7:40351582
|
T | C | 2 | a0001c0001t0001g0003a0001c0002t0001g0001 | 2 | HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+34727T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40351582 | ||||||
| chr7:40352670
|
A | T | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.816+35815A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40352670 | ||||||
| chr7:40352739
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+35884G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40352739 | ||||||
| chr7:40353065
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.816+36210C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40353065 | ||||||
| chr7:40354641
|
AG | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+37790delG | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40354641 | |||||
| chr7:40355018
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+38163A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40355018 | ||||||
| chr7:40356701
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+39846T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40356701 | ||||||
| chr7:40356767
|
C | G | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+39912C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40356767 | ||||||
| chr7:40357974
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+41119G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40357974 | ||||||
| chr7:40358540
|
C | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+41685C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40358540 | ||||||
| chr7:40358617
|
A | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+41762A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40358617 | ||||||
| chr7:40358629
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+41774G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40358629 | ||||||
| chr7:40358717
|
A | AAACAAC | 2 | a0001c0001t0001g0003a0001c0002t0001g0001 | 2 | HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+41871_816+4187 others(10): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40358717 | |||||
| chr7:40358732
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+41877T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40358732 | ||||||
| chr7:40359425
|
A | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+42570A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40359425 | ||||||
| chr7:40359936
|
C | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+43081C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40359936 | ||||||
| chr7:40360044
|
C | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.816+43189C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40360044 | ||||||
| chr7:40361371
|
G | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.816+44516G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40361371 | ||||||
| chr7:40361588
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+44733G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40361588 | ||||||
| chr7:40361761
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+44906C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40361761 | ||||||
| chr7:40361777
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+44922G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40361777 | ||||||
| chr7:40362048
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+45193T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40362048 | ||||||
| chr7:40362341
|
C | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+45486C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40362341 | ||||||
| chr7:40362443
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+45588G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40362443 | ||||||
| chr7:40362831
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+45976A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40362831 | ||||||
| chr7:40364133
|
A | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+47278A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40364133 | ||||||
| chr7:40366127
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.816+49272G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40366127 | ||||||
| chr7:40366970
|
G | GTTTATTG others(5): Show |
1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+50116_816+5012 others(16): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40366970 | |||||
| chr7:40367385
|
T | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+50530T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40367385 | ||||||
| chr7:40367450
|
GA | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+50605delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40367450 | |||||
| chr7:40367874
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+51019G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40367874 | ||||||
| chr7:40368715
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+51860T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40368715 | ||||||
| chr7:40369807
|
A | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+52952A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40369807 | ||||||
| chr7:40369950
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+53095G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40369950 | ||||||
| chr7:40371726
|
CTTAA | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+54874_816+5487 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40371726 | |||||
| chr7:40373132
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+56277G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40373132 | ||||||
| chr7:40373288
|
C | CAGAATCT others(168): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+56517_816+5651 others(179): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40373288 | |||||
| chr7:40373288
|
C | CAGAATCT others(218): Show |
1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+56517_816+5651 others(229): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40373288 | |||||
| chr7:40373298
|
A | AGATTCTA others(143): Show |
1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+56517_816+5651 others(154): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40373298 | |||||
| chr7:40373298
|
A | AGATTCTA others(168): Show |
1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.816+56517_816+5651 others(179): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40373298 | |||||
| chr7:40373323
|
A | AGATTCTA others(168): Show |
1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.816+56517_816+5651 others(179): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40373323 | |||||
| chr7:40373323
|
A | AGATTCTA others(143): Show |
1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.816+56518_816+5651 others(154): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40373323 | |||||
| chr7:40374960
|
A | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+58105A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40374960 | ||||||
| chr7:40375718
|
A | ATTGTT | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+58867_816+5886 others(9): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40375718 | |||||
| chr7:40376221
|
G | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+59366G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40376221 | ||||||
| chr7:40376746
|
C | CT | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+59902dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40376746 | |||||
| chr7:40376957
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+60102G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40376957 | ||||||
| chr7:40377088
|
ATG | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+60235_816+6023 others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40377088 | |||||
| chr7:40377126
|
TCC | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.816+60272_816+6027 others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377126 | ||||||
| chr7:40377127
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(1): Show | 4 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+60272C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377127 | ||||||
| chr7:40377128
|
C | CTT | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+60274_816+6027 others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40377128 | |||||
| chr7:40377199
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.816+60344T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377199 | ||||||
| chr7:40377199
|
T | TTTC | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006 | 3 | HG00738.hp1 HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.816+60346_816+6034 others(7): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40377199 | |||||
| chr7:40377201
|
T | C | 2 | a0001c0002t0001g0001a0001c0003t0001g0005 | 2 | HG01192.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.816+60346T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377201 | ||||||
| chr7:40377203
|
C | T | 2 | a0001c0002t0001g0001a0001c0003t0001g0005 | 2 | HG01192.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.816+60348C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377203 | ||||||
| chr7:40377205
|
T | C | 2 | a0001c0002t0001g0001a0001c0003t0001g0005 | 2 | HG01192.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.816+60350T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377205 | ||||||
| chr7:40377208
|
C | T | 3 | a0001c0001t0001g0004a0001c0002t0001g0001a0001c0003t0001g0005 | 3 | HG00738.hp1 HG01192.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.816+60353C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377208 | ||||||
| chr7:40377209
|
T | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+60354T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377209 | ||||||
| chr7:40377218
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0008 | 2 | HG00738.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+60363T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377218 | ||||||
| chr7:40377218
|
T | TTTC | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+60365_816+6036 others(7): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40377218 | |||||
| chr7:40377233
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+60378C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377233 | ||||||
| chr7:40377235
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(3): Show | 6 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+60380C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377235 | ||||||
| chr7:40377238
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+60383C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377238 | ||||||
| chr7:40377239
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+60384C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377239 | ||||||
| chr7:40377242
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+60387C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377242 | ||||||
| chr7:40377243
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+60388C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377243 | ||||||
| chr7:40377244
|
T | A | 1 | a0001c0001t0001g0007 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.816+60389T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377244 | ||||||
| chr7:40377246
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+60391C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377246 | ||||||
| chr7:40377247
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(3): Show | 6 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+60392C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377247 | ||||||
| chr7:40377248
|
T | TTTCTTTC others(3): Show |
1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+60394_816+6039 others(14): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40377248 | |||||
| chr7:40377253
|
TC | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+60399delC | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40377253 | ||||||
| chr7:40377254
|
C | CTTTCCTT others(46): Show |
1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.816+60402_816+6040 others(57): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40377254 | |||||
| chr7:40377254
|
C | CTTTCTTT others(54): Show |
1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.816+60402_816+6040 others(65): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40377254 | |||||
| chr7:40377254
|
C | CTTTCTTT others(82): Show |
1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+60402_816+6040 others(93): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40377254 | |||||
| chr7:40377254
|
C | CTTTCTTT others(90): Show |
1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.816+60402_816+6040 others(101): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40377254 | |||||
| chr7:40378114
|
AT | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+61269delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40378114 | |||||
| chr7:40378132
|
AG | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+61278delG | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40378132 | ||||||
| chr7:40378326
|
A | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+61471A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40378326 | ||||||
| chr7:40378541
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+61686C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40378541 | ||||||
| chr7:40378992
|
G | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+62137G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40378992 | ||||||
| chr7:40379071
|
G | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+62216G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40379071 | ||||||
| chr7:40379174
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.816+62319G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40379174 | ||||||
| chr7:40379294
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+62439G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40379294 | ||||||
| chr7:40379346
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+62491G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40379346 | ||||||
| chr7:40379593
|
T | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+62738T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40379593 | ||||||
| chr7:40379631
|
A | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+62776A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40379631 | ||||||
| chr7:40379970
|
A | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+63115A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40379970 | ||||||
| chr7:40380134
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.816+63279G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40380134 | ||||||
| chr7:40380433
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+63578A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40380433 | ||||||
| chr7:40381046
|
T | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+64191T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40381046 | ||||||
| chr7:40381302
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+64447A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40381302 | ||||||
| chr7:40381474
|
A | ACT | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+64619_816+6462 others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40381474 | ||||||
| chr7:40381859
|
T | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.816+65004T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40381859 | ||||||
| chr7:40381889
|
T | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+65034T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40381889 | ||||||
| chr7:40382015
|
C | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+65160C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40382015 | ||||||
| chr7:40382543
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+65688T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40382543 | ||||||
| chr7:40382989
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+66134T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40382989 | ||||||
| chr7:40383051
|
A | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+66196A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40383051 | ||||||
| chr7:40383649
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.817-65638A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40383649 | ||||||
| chr7:40384290
|
A | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-64997A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40384290 | ||||||
| chr7:40384757
|
CTGGTTT | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-64527_817-6452 others(10): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40384757 | |||||
| chr7:40384899
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-64388T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40384899 | ||||||
| chr7:40385309
|
G | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.817-63978G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40385309 | ||||||
| chr7:40385541
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-63746G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40385541 | ||||||
| chr7:40385567
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-63720T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40385567 | ||||||
| chr7:40385725
|
CT | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-63559delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40385725 | |||||
| chr7:40386783
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.817-62504G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40386783 | ||||||
| chr7:40388018
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-61269T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40388018 | ||||||
| chr7:40388315
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.817-60972A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40388315 | ||||||
| chr7:40388803
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-60484G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40388803 | ||||||
| chr7:40388997
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.817-60290T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40388997 | ||||||
| chr7:40389267
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-60020C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40389267 | ||||||
| chr7:40389307
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-59980G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40389307 | ||||||
| chr7:40389442
|
A | AAAACAAA others(5): Show |
1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.817-59826_817-5981 others(16): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40389442 | |||||
| chr7:40389442
|
AAAAC | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-59818_817-5981 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40389442 | |||||
| chr7:40389469
|
A | ACAAACAA others(5): Show |
2 | a0001c0001t0001g0003a0001c0002t0001g0001 | 2 | HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.817-59815_817-5981 others(16): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40389469 | |||||
| chr7:40389711
|
C | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.817-59576C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40389711 | ||||||
| chr7:40390419
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-58868T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40390419 | ||||||
| chr7:40390455
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-58832A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40390455 | ||||||
| chr7:40390591
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-58696C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40390591 | ||||||
| chr7:40390671
|
A | T | 2 | a0001c0001t0001g0004a0001c0002t0001g0001 | 2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.817-58616A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40390671 | ||||||
| chr7:40390700
|
G | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-58587G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40390700 | ||||||
| chr7:40391079
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.817-58208A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40391079 | ||||||
| chr7:40391596
|
AC | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-57689delC | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40391596 | |||||
| chr7:40391598
|
C | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-57689C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40391598 | ||||||
| chr7:40392161
|
A | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-57126A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40392161 | ||||||
| chr7:40392369
|
A | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-56918A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40392369 | ||||||
| chr7:40393104
|
T | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-56183T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40393104 | ||||||
| chr7:40393991
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-55296C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40393991 | ||||||
| chr7:40397025
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-52262A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40397025 | ||||||
| chr7:40397164
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-52123T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40397164 | ||||||
| chr7:40397851
|
C | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-51436C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40397851 | ||||||
| chr7:40398166
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-51121G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40398166 | ||||||
| chr7:40398177
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-51110C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40398177 | ||||||
| chr7:40398515
|
CT | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-50755delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40398515 | |||||
| chr7:40398515
|
CTT | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-50756_817-5075 others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40398515 | |||||
| chr7:40399068
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-50219T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40399068 | ||||||
| chr7:40400000
|
A | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-49287A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40400000 | ||||||
| chr7:40400961
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-48326G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40400961 | ||||||
| chr7:40400974
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-48313G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40400974 | ||||||
| chr7:40402463
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-46824G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40402463 | ||||||
| chr7:40403055
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-46232G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40403055 | ||||||
| chr7:40403142
|
A | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-46145A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40403142 | ||||||
| chr7:40403653
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-45634C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40403653 | ||||||
| chr7:40405299
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.817-43988A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40405299 | ||||||
| chr7:40405764
|
A | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-43523A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40405764 | ||||||
| chr7:40405808
|
TA | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-43457delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40405808 | |||||
| chr7:40406346
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.817-42941T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40406346 | ||||||
| chr7:40407280
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-42007T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40407280 | ||||||
| chr7:40409071
|
C | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.817-40216C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40409071 | ||||||
| chr7:40409275
|
AT | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.817-40006delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40409275 | |||||
| chr7:40410612
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.817-38675A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40410612 | ||||||
| chr7:40410852
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-38435G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40410852 | ||||||
| chr7:40410968
|
A | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-38319A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40410968 | ||||||
| chr7:40411860
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-37427G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40411860 | ||||||
| chr7:40411950
|
AT | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-37330delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40411950 | |||||
| chr7:40411991
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.817-37296T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40411991 | ||||||
| chr7:40412044
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-37243A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40412044 | ||||||
| chr7:40412959
|
A | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-36328A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40412959 | ||||||
| chr7:40413262
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-36025T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40413262 | ||||||
| chr7:40413815
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-35472T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40413815 | ||||||
| chr7:40415061
|
A | ATCTATCT | 2 | a0001c0001t0001g0004a0001c0003t0001g0005 | 2 | HG00738.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.817-34226_817-3422 others(11): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40415061 | ||||||
| chr7:40415061
|
A | ATCTATCT others(8): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-34226_817-3422 others(19): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40415061 | ||||||
| chr7:40415062
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-34225A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40415062 | ||||||
| chr7:40415107
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-34180T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40415107 | ||||||
| chr7:40415268
|
C | CA | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-34000dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40415268 | |||||
| chr7:40417672
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-31615G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40417672 | ||||||
| chr7:40417729
|
G | GTTTT | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-31558_817-3155 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40417729 | ||||||
| chr7:40417758
|
T | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-31529T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40417758 | ||||||
| chr7:40417900
|
T | TTC | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-31386_817-3138 others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40417900 | |||||
| chr7:40418705
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-30582A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40418705 | ||||||
| chr7:40419400
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.817-29887T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40419400 | ||||||
| chr7:40420130
|
C | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-29157C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40420130 | ||||||
| chr7:40420590
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-28697C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40420590 | ||||||
| chr7:40420902
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.817-28385G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40420902 | ||||||
| chr7:40421717
|
T | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.817-27570T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40421717 | ||||||
| chr7:40421733
|
G | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-27554G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40421733 | ||||||
| chr7:40422324
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-26963G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40422324 | ||||||
| chr7:40423355
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.817-25932G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40423355 | ||||||
| chr7:40424266
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.817-25021T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40424266 | ||||||
| chr7:40425295
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-23992T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40425295 | ||||||
| chr7:40426601
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.817-22686C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40426601 | ||||||
| chr7:40427652
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.817-21635T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40427652 | ||||||
| chr7:40428522
|
CTGTG | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-20733_817-2073 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40428522 | |||||
| chr7:40428522
|
CTGTGTGT others(1): Show |
C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-20737_817-2073 others(12): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40428522 | |||||
| chr7:40428692
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.817-20595A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40428692 | ||||||
| chr7:40429122
|
GT | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-20155delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40429122 | |||||
| chr7:40430620
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.817-18667C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40430620 | ||||||
| chr7:40432685
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0003t0001g0005 | 3 | HG00738.hp1 HG01069.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.817-16583_817-1657 others(15): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40432685 | |||||
| chr7:40432685
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.817-16584_817-1657 others(16): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40432685 | |||||
| chr7:40433293
|
G | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-15994G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40433293 | ||||||
| chr7:40433405
|
C | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-15882C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40433405 | ||||||
| chr7:40434000
|
A | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-15287A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40434000 | ||||||
| chr7:40434151
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-15136C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40434151 | ||||||
| chr7:40434416
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-14871C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40434416 | ||||||
| chr7:40435926
|
C | CTTTCT | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-13342_817-1333 others(9): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40435926 | |||||
| chr7:40435926
|
C | CTTTCTTT others(3): Show |
1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.817-13347_817-1333 others(14): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40435926 | |||||
| chr7:40435945
|
CT | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-13326delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40435945 | |||||
| chr7:40437026
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-12261C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40437026 | ||||||
| chr7:40437459
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-11828T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40437459 | ||||||
| chr7:40437761
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-11526G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40437761 | ||||||
| chr7:40437764
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-11523A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40437764 | ||||||
| chr7:40438379
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.817-10908A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40438379 | ||||||
| chr7:40439061
|
G | GGTAT | 2 | a0001c0002t0001g0001a0001c0003t0001g0005 | 2 | HG01192.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.817-10224_817-1022 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40439061 | |||||
| chr7:40439064
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-10223G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40439064 | ||||||
| chr7:40439072
|
A | ATG | 2 | a0001c0001t0001g0002a0001c0001t0001g0006 | 2 | HG00738.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.817-10214_817-1021 others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40439072 | |||||
| chr7:40439072
|
A | ATGTG | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-10214_817-1021 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40439072 | |||||
| chr7:40439074
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-10213A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40439074 | ||||||
| chr7:40439076
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-10211A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40439076 | ||||||
| chr7:40439078
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.817-10209A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40439078 | ||||||
| chr7:40440124
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-9163G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40440124 | ||||||
| chr7:40440145
|
GTTTT | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-9113_817-9110d others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40440145 | |||||
| chr7:40440160
|
T | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-9127T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40440160 | ||||||
| chr7:40440253
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-9034G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40440253 | ||||||
| chr7:40440460
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.817-8827C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40440460 | ||||||
| chr7:40442096
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-7191G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40442096 | ||||||
| chr7:40442213
|
A | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-7074A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40442213 | ||||||
| chr7:40444977
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-4310G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40444977 | ||||||
| chr7:40445246
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.817-4041G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40445246 | ||||||
| chr7:40446336
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-2951C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40446336 | ||||||
| chr7:40448214
|
T | TTCCC | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.817-1043_817-1040d others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40448214 | |||||
| chr7:40448214
|
T | TTCCCTCC others(5): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-1051_817-1040d others(14): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40448214 | |||||
| chr7:40448526
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-761C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40448526 | ||||||
| chr7:40448629
|
C | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.817-658C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40448629 | ||||||
| chr7:40448807
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-480T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40448807 | ||||||
| chr7:40448904
|
ATG | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-369_817-368del others(2): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 40448904 | |||||
| chr7:40448920
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.817-367A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40448920 | ||||||
| chr7:40448926
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.817-361G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40448926 | ||||||
| chr7:40448950
|
G | A | 2 | a0001c0002t0001g0001a0001c0003t0001g0005 | 2 | HG01192.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.817-337G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40448950 | ||||||
| chr7:40448959
|
T | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.817-328T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40448959 | ||||||
| chr7:40448961
|
T | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.817-326T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40448961 | ||||||
| chr7:40448963
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01069.hp1 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.817-324G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40448963 | ||||||
| chr7:40449253
|
A | C | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.817-34A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 9/13 | chr7 | 40449253 | ||||||
| chr7:40449484
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0001 | 3 | HG01069.hp2 HG01192.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.888+126C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40449484 | ||||||
| chr7:40449770
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.888+412C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40449770 | ||||||
| chr7:40449997
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.888+639T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40449997 | ||||||
| chr7:40450773
|
C | CA | 3 | a0001c0001t0001g0002a0001c0002t0001g0001a0001c0003t0001g0005 | 3 | HG01192.hp2 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.888+1426dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 40450773 | |||||
| chr7:40450907
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.888+1549G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40450907 | ||||||
| chr7:40450909
|
T | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.888+1551T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40450909 | ||||||
| chr7:40451077
|
C | G | 2 | a0001c0001t0001g0002a0001c0003t0001g0005 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.888+1719C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40451077 | ||||||
| chr7:40452935
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.888+3577C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40452935 | ||||||
| chr7:40452982
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.888+3624C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40452982 | ||||||
| chr7:40453595
|
G | C | 2 | a0001c0001t0001g0002a0001c0003t0001g0005 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.888+4237G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40453595 | ||||||
| chr7:40454109
|
G | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.888+4751G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40454109 | ||||||
| chr7:40454436
|
T | A | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.889-4665T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40454436 | ||||||
| chr7:40454618
|
G | GA | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.889-4477dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 40454618 | |||||
| chr7:40457215
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.889-1886A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40457215 | ||||||
| chr7:40457679
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.889-1422G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40457679 | ||||||
| chr7:40457713
|
C | T | 2 | a0001c0001t0001g0002a0001c0003t0001g0005 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.889-1388C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40457713 | ||||||
| chr7:40458475
|
C | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.889-626C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40458475 | ||||||
| chr7:40458923
|
C | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.889-178C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40458923 | ||||||
| chr7:40458983
|
A | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.889-118A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40458983 | ||||||
| chr7:40459033
|
A | C | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.889-68A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 10/13 | chr7 | 40459033 | ||||||
| chr7:40459230
|
G | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.986+32G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40459230 | ||||||
| chr7:40459374
|
T | C | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.986+176T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40459374 | ||||||
| chr7:40459423
|
A | C | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.986+225A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40459423 | ||||||
| chr7:40460115
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.986+917C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40460115 | ||||||
| chr7:40460212
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.986+1014T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40460212 | ||||||
| chr7:40461357
|
C | T | 2 | a0001c0001t0001g0002a0001c0003t0001g0005 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.986+2159C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40461357 | ||||||
| chr7:40461772
|
G | C | 2 | a0001c0001t0001g0002a0001c0003t0001g0005 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.986+2574G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40461772 | ||||||
| chr7:40462396
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.986+3198A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40462396 | ||||||
| chr7:40462449
|
A | AT | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.986+3260dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40462449 | |||||
| chr7:40462569
|
G | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.986+3371G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40462569 | ||||||
| chr7:40462811
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.986+3613G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40462811 | ||||||
| chr7:40464303
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.986+5105G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40464303 | ||||||
| chr7:40464843
|
T | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.986+5645T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40464843 | ||||||
| chr7:40464952
|
G | A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.986+5754G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40464952 | ||||||
| chr7:40465124
|
A | G | 2 | a0001c0001t0001g0002a0001c0003t0001g0005 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.986+5926A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40465124 | ||||||
| chr7:40465320
|
C | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.986+6122C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40465320 | ||||||
| chr7:40465734
|
G | A | 2 | a0001c0001t0001g0002a0001c0003t0001g0005 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.986+6536G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40465734 | ||||||
| chr7:40465783
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.986+6585A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40465783 | ||||||
| chr7:40466068
|
T | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.986+6870T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40466068 | ||||||
| chr7:40466170
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.986+6972A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40466170 | ||||||
| chr7:40466800
|
T | C | 2 | a0001c0001t0001g0002a0001c0003t0001g0005 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.986+7602T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40466800 | ||||||
| chr7:40466920
|
C | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.986+7722C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40466920 | ||||||
| chr7:40467204
|
G | GA | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.986+8028dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40467204 | |||||
| chr7:40467227
|
G | A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.986+8029G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40467227 | ||||||
| chr7:40467809
|
G | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.986+8611G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40467809 | ||||||
| chr7:40467986
|
C | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.986+8788C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40467986 | ||||||
| chr7:40467987
|
T | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.986+8789T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40467987 | ||||||
| chr7:40468126
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.986+8928A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40468126 | ||||||
| chr7:40468253
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.986+9055C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40468253 | ||||||
| chr7:40468421
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.986+9223C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40468421 | ||||||
| chr7:40468709
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.986+9511A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40468709 | ||||||
| chr7:40469519
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.986+10321C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40469519 | ||||||
| chr7:40469699
|
T | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.986+10501T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40469699 | ||||||
| chr7:40469721
|
G | GT | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.986+10533dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40469721 | |||||
| chr7:40470747
|
G | GTCTC | 2 | a0001c0001t0001g0004a0001c0003t0001g0005 | 2 | HG00738.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.986+11579_986+1158 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40470747 | |||||
| chr7:40470747
|
GTC | G | 2 | a0001c0001t0001g0006a0001c0002t0001g0001 | 2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.986+11581_986+1158 others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40470747 | |||||
| chr7:40471087
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.986+11889G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40471087 | ||||||
| chr7:40475122
|
G | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.986+15924G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40475122 | ||||||
| chr7:40475143
|
G | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.986+15945G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40475143 | ||||||
| chr7:40475270
|
G | A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.986+16072G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40475270 | ||||||
| chr7:40475883
|
AAATTATC others(4): Show |
A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.986+16689_986+1669 others(15): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40475883 | |||||
| chr7:40476028
|
C | T | 2 | a0001c0001t0001g0002a0001c0003t0001g0005 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.986+16830C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40476028 | ||||||
| chr7:40476801
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.986+17603A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40476801 | ||||||
| chr7:40478604
|
A | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.987-17680A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40478604 | ||||||
| chr7:40478771
|
C | A | 2 | a0001c0001t0001g0002a0001c0003t0001g0005 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.987-17513C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40478771 | ||||||
| chr7:40480143
|
C | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.987-16141C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40480143 | ||||||
| chr7:40480458
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.987-15826G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40480458 | ||||||
| chr7:40481169
|
G | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.987-15115G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40481169 | ||||||
| chr7:40481226
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.987-15058C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40481226 | ||||||
| chr7:40481561
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.987-14723G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40481561 | ||||||
| chr7:40482088
|
T | C | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.987-14196T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40482088 | ||||||
| chr7:40482220
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.987-14064A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40482220 | ||||||
| chr7:40482394
|
CA | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.987-13888delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40482394 | |||||
| chr7:40483697
|
GA | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.987-12574delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40483697 | |||||
| chr7:40483932
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.987-12352G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40483932 | ||||||
| chr7:40484457
|
G | A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.987-11827G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40484457 | ||||||
| chr7:40484543
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.987-11741C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40484543 | ||||||
| chr7:40485417
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.987-10853_987-1084 others(16): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40485417 | |||||
| chr7:40486366
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.987-9918A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40486366 | ||||||
| chr7:40486701
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.987-9583T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40486701 | ||||||
| chr7:40486724
|
C | CT | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-9546dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40486724 | |||||
| chr7:40487014
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.987-9270C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40487014 | ||||||
| chr7:40487944
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.987-8340A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40487944 | ||||||
| chr7:40489259
|
T | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.987-7025T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40489259 | ||||||
| chr7:40489733
|
A | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.987-6551A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40489733 | ||||||
| chr7:40489987
|
A | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.987-6297A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40489987 | ||||||
| chr7:40490064
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.987-6220G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40490064 | ||||||
| chr7:40490133
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.987-6151A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40490133 | ||||||
| chr7:40490825
|
A | AT | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.987-5451dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40490825 | |||||
| chr7:40490949
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.987-5335G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40490949 | ||||||
| chr7:40491055
|
TATTCTTT others(7): Show |
T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.987-5226_987-5213d others(16): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40491055 | |||||
| chr7:40491133
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.987-5151G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40491133 | ||||||
| chr7:40491609
|
T | A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.987-4675T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40491609 | ||||||
| chr7:40491652
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.987-4632G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40491652 | ||||||
| chr7:40491659
|
CA | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.987-4615delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40491659 | |||||
| chr7:40491992
|
A | AAAAT | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.987-4269_987-4266d others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40491992 | |||||
| chr7:40491992
|
A | AAAATAAA others(1): Show |
2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.987-4273_987-4266d others(10): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40491992 | |||||
| chr7:40492655
|
G | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.987-3629G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40492655 | ||||||
| chr7:40494904
|
T | TTTTG | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.987-1364_987-1361d others(6): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40494904 | |||||
| chr7:40494925
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.987-1359T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | chr7 | 40494925 | ||||||
| chr7:40495227
|
C | CT | 3 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.987-1042dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 40495227 | |||||
| chr7:40496736
|
T | TACCTCTG others(18): Show |
4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089+371_1089+395d others(27): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40496736 | |||||
| chr7:40497822
|
T | C | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1089+1436T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40497822 | ||||||
| chr7:40498051
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1089+1665C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40498051 | ||||||
| chr7:40499211
|
A | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089+2825A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40499211 | ||||||
| chr7:40499826
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+3440T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40499826 | ||||||
| chr7:40499876
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1089+3490G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40499876 | ||||||
| chr7:40500345
|
T | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1089+3959T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40500345 | ||||||
| chr7:40500808
|
T | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.1089+4422T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40500808 | ||||||
| chr7:40500884
|
AACACAT | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+4516_1089+452 others(10): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40500884 | |||||
| chr7:40501017
|
C | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1089+4631C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40501017 | ||||||
| chr7:40501493
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1089+5107T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40501493 | ||||||
| chr7:40501620
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1089+5234C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40501620 | ||||||
| chr7:40501660
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089+5274T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40501660 | ||||||
| chr7:40503892
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1089+7506G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40503892 | ||||||
| chr7:40503912
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1089+7526G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40503912 | ||||||
| chr7:40504383
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1089+7997G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40504383 | ||||||
| chr7:40506007
|
G | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+9621G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40506007 | ||||||
| chr7:40506527
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+10141C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40506527 | ||||||
| chr7:40507323
|
G | T | 2 | a0001c0001t0001g0002a0001c0002t0001g0001 | 2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1089+10937G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40507323 | ||||||
| chr7:40508674
|
A | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+12288A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40508674 | ||||||
| chr7:40509061
|
A | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1089+12675A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40509061 | ||||||
| chr7:40509358
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+12972T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40509358 | ||||||
| chr7:40509990
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1089+13604A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40509990 | ||||||
| chr7:40512424
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+16038C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40512424 | ||||||
| chr7:40513355
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+16969T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40513355 | ||||||
| chr7:40514538
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+18152A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40514538 | ||||||
| chr7:40514570
|
T | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.1089+18184T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40514570 | ||||||
| chr7:40515493
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+19107G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40515493 | ||||||
| chr7:40515884
|
C | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+19498C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40515884 | ||||||
| chr7:40517313
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+20927T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40517313 | ||||||
| chr7:40518396
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+22010A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40518396 | ||||||
| chr7:40518781
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1089+22395A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40518781 | ||||||
| chr7:40520137
|
C | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+23751C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40520137 | ||||||
| chr7:40520436
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+24050G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40520436 | ||||||
| chr7:40520900
|
C | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+24514C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40520900 | ||||||
| chr7:40523340
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+26954A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40523340 | ||||||
| chr7:40524185
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+27799T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40524185 | ||||||
| chr7:40525153
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+28767A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40525153 | ||||||
| chr7:40525841
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1089+29455G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40525841 | ||||||
| chr7:40525891
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+29505G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40525891 | ||||||
| chr7:40528929
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+32543A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40528929 | ||||||
| chr7:40531638
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+35252A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40531638 | ||||||
| chr7:40531714
|
C | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+35328C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40531714 | ||||||
| chr7:40532402
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+36016A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40532402 | ||||||
| chr7:40532526
|
C | CTG | 4 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp1 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089+36182_1089+36 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40532526 | |||||
| chr7:40532998
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+36612T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40532998 | ||||||
| chr7:40533280
|
G | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+36894G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40533280 | ||||||
| chr7:40534714
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1089+38328C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40534714 | ||||||
| chr7:40536642
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+40256T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40536642 | ||||||
| chr7:40536888
|
G | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+40502G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40536888 | ||||||
| chr7:40539078
|
C | CA | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+42710dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40539078 | |||||
| chr7:40539097
|
T | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+42711T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40539097 | ||||||
| chr7:40542518
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+46132A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40542518 | ||||||
| chr7:40543109
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+46723C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40543109 | ||||||
| chr7:40543218
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+46832G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40543218 | ||||||
| chr7:40544247
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+47861A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40544247 | ||||||
| chr7:40544345
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1089+47959G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40544345 | ||||||
| chr7:40544570
|
C | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+48184C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40544570 | ||||||
| chr7:40546467
|
T | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+50081T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40546467 | ||||||
| chr7:40546474
|
C | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+50088C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40546474 | ||||||
| chr7:40547072
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.1089+50686C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40547072 | ||||||
| chr7:40547075
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+50689G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40547075 | ||||||
| chr7:40548020
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1089+51634G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40548020 | ||||||
| chr7:40548186
|
C | CT | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG00738.hp1 HG00738.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1089+51820dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40548186 | |||||
| chr7:40550655
|
G | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+54269G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40550655 | ||||||
| chr7:40550678
|
G | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+54292G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40550678 | ||||||
| chr7:40550970
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+54584C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40550970 | ||||||
| chr7:40551376
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+54990C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40551376 | ||||||
| chr7:40551836
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1089+55450G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40551836 | ||||||
| chr7:40552148
|
G | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+55762G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40552148 | ||||||
| chr7:40552207
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+55821G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40552207 | ||||||
| chr7:40552287
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+55901A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40552287 | ||||||
| chr7:40556917
|
G | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+60531G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40556917 | ||||||
| chr7:40557570
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+61184C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40557570 | ||||||
| chr7:40560328
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+63942A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40560328 | ||||||
| chr7:40561753
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+65367A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40561753 | ||||||
| chr7:40561884
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+65498G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40561884 | ||||||
| chr7:40562073
|
C | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+65687C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40562073 | ||||||
| chr7:40562506
|
T | G | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1089+66120T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40562506 | ||||||
| chr7:40562824
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+66438C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40562824 | ||||||
| chr7:40563238
|
G | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+66852G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40563238 | ||||||
| chr7:40564024
|
C | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+67638C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40564024 | ||||||
| chr7:40564371
|
C | T | 2 | a0001c0001t0001g0003a0001c0002t0001g0001 | 2 | HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1089+67985C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40564371 | ||||||
| chr7:40564738
|
G | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+68352G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40564738 | ||||||
| chr7:40565981
|
ACACACAC others(5): Show |
A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+69607_1089+69 others(18): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40565981 | |||||
| chr7:40565993
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+69607G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40565993 | ||||||
| chr7:40565997
|
A | ACG | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+69612_1089+69 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40565997 | |||||
| chr7:40565999
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+69613A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40565999 | ||||||
| chr7:40570485
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+74099A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40570485 | ||||||
| chr7:40571005
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+74619A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40571005 | ||||||
| chr7:40572424
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1089+76038T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40572424 | ||||||
| chr7:40572427
|
T | G | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1089+76041T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40572427 | ||||||
| chr7:40572605
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+76219G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40572605 | ||||||
| chr7:40572628
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089+76242G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40572628 | ||||||
| chr7:40572651
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+76265A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40572651 | ||||||
| chr7:40574272
|
C | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+77886C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40574272 | ||||||
| chr7:40574654
|
C | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+78268C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40574654 | ||||||
| chr7:40575125
|
T | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+78739T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40575125 | ||||||
| chr7:40575126
|
G | GGC | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+78741_1089+78 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40575126 | |||||
| chr7:40575246
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+78860G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40575246 | ||||||
| chr7:40575979
|
A | T | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1089+79593A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40575979 | ||||||
| chr7:40579078
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+82692T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40579078 | ||||||
| chr7:40579396
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+83010A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40579396 | ||||||
| chr7:40580495
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1089+84109A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40580495 | ||||||
| chr7:40583289
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+86903T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40583289 | ||||||
| chr7:40583715
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+87329C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40583715 | ||||||
| chr7:40583927
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+87541C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40583927 | ||||||
| chr7:40585742
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+89356T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40585742 | ||||||
| chr7:40586540
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1089+90154G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40586540 | ||||||
| chr7:40587918
|
T | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+91532T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40587918 | ||||||
| chr7:40588193
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+91807C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40588193 | ||||||
| chr7:40589161
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1089+92775T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40589161 | ||||||
| chr7:40589910
|
C | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+93524C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40589910 | ||||||
| chr7:40590785
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1089+94399A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40590785 | ||||||
| chr7:40591542
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+95156T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40591542 | ||||||
| chr7:40592098
|
A | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+95712A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40592098 | ||||||
| chr7:40592227
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+95841C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40592227 | ||||||
| chr7:40593123
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.1089+96737A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40593123 | ||||||
| chr7:40593862
|
C | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+97476C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40593862 | ||||||
| chr7:40594249
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+97863G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40594249 | ||||||
| chr7:40594421
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+98035G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40594421 | ||||||
| chr7:40594716
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+98330T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40594716 | ||||||
| chr7:40594783
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+98397A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40594783 | ||||||
| chr7:40595369
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1089+98983T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40595369 | ||||||
| chr7:40598502
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+102116C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40598502 | ||||||
| chr7:40598716
|
G | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+102330G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40598716 | ||||||
| chr7:40598766
|
T | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+102380T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40598766 | ||||||
| chr7:40598944
|
C | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+102558C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40598944 | ||||||
| chr7:40599931
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+103545G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40599931 | ||||||
| chr7:40599974
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+103588C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40599974 | ||||||
| chr7:40602210
|
A | T | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1089+105824A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40602210 | ||||||
| chr7:40602370
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+105984G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40602370 | ||||||
| chr7:40602448
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+106062C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40602448 | ||||||
| chr7:40604489
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+108103G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40604489 | ||||||
| chr7:40605662
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+109276A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40605662 | ||||||
| chr7:40606046
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+109660G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40606046 | ||||||
| chr7:40606702
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+110316T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40606702 | ||||||
| chr7:40607550
|
C | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+111164C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40607550 | ||||||
| chr7:40608611
|
T | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+112225T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40608611 | ||||||
| chr7:40609342
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+112956G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40609342 | ||||||
| chr7:40609348
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+112962C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40609348 | ||||||
| chr7:40609446
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+113060C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40609446 | ||||||
| chr7:40609484
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+113098A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40609484 | ||||||
| chr7:40611256
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+114870G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40611256 | ||||||
| chr7:40612013
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+115627T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40612013 | ||||||
| chr7:40612188
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1089+115802T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40612188 | ||||||
| chr7:40612875
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+116489G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40612875 | ||||||
| chr7:40614084
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1089+117698C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40614084 | ||||||
| chr7:40614085
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.1089+117699A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40614085 | ||||||
| chr7:40614163
|
G | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+117777G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40614163 | ||||||
| chr7:40615301
|
A | AT | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+118922dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40615301 | |||||
| chr7:40615681
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1089+119295G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40615681 | ||||||
| chr7:40616440
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+120054C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40616440 | ||||||
| chr7:40616676
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+120290A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40616676 | ||||||
| chr7:40616798
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+120412A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40616798 | ||||||
| chr7:40617013
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+120627A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40617013 | ||||||
| chr7:40617159
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1089+120773A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40617159 | ||||||
| chr7:40617475
|
A | ATG | 2 | a0001c0001t0001g0004a0001c0001t0001g0006 | 2 | HG00738.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.1089+121126_1089+1 others(10): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40617475 | |||||
| chr7:40617475
|
ATG | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1089+121126_1089+1 others(10): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40617475 | |||||
| chr7:40618681
|
C | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+122295C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40618681 | ||||||
| chr7:40619330
|
A | G | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1089+122944A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40619330 | ||||||
| chr7:40621041
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+124655C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40621041 | ||||||
| chr7:40621134
|
A | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+124748A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40621134 | ||||||
| chr7:40622755
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+126369G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40622755 | ||||||
| chr7:40622823
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089+126437T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40622823 | ||||||
| chr7:40624024
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-125410A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40624024 | ||||||
| chr7:40624135
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-125299G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40624135 | ||||||
| chr7:40624310
|
A | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-125124A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40624310 | ||||||
| chr7:40624772
|
AACACAC | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006 | 3 | HG00738.hp2 HG01069.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1090-124627_1090-1 others(14): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40624772 | |||||
| chr7:40624805
|
ACACACAC others(1): Show |
A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-124623_1090-1 others(16): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40624805 | |||||
| chr7:40625812
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1090-123622T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40625812 | ||||||
| chr7:40626211
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1090-123223G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40626211 | ||||||
| chr7:40626882
|
A | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-122552A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40626882 | ||||||
| chr7:40629699
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-119735C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40629699 | ||||||
| chr7:40631635
|
G | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1090-117799G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40631635 | ||||||
| chr7:40633090
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1090-116344T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40633090 | ||||||
| chr7:40636100
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-113334A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40636100 | ||||||
| chr7:40636957
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-112477T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40636957 | ||||||
| chr7:40638536
|
T | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-110898T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40638536 | ||||||
| chr7:40640156
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1090-109278A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40640156 | ||||||
| chr7:40643746
|
C | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-105688C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40643746 | ||||||
| chr7:40644052
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-105382A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40644052 | ||||||
| chr7:40644253
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1090-105181C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40644253 | ||||||
| chr7:40646212
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090-103222T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40646212 | ||||||
| chr7:40646289
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1090-103145C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40646289 | ||||||
| chr7:40646856
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-102578T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40646856 | ||||||
| chr7:40647551
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-101883G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40647551 | ||||||
| chr7:40647766
|
G | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-101668G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40647766 | ||||||
| chr7:40648385
|
G | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-101049G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40648385 | ||||||
| chr7:40650266
|
G | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-99168G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40650266 | ||||||
| chr7:40650328
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-99106G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40650328 | ||||||
| chr7:40651269
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-98165C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40651269 | ||||||
| chr7:40651327
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-98107A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40651327 | ||||||
| chr7:40651630
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-97804T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40651630 | ||||||
| chr7:40652850
|
A | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-96584A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40652850 | ||||||
| chr7:40654549
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0006 | 2 | HG00738.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.1090-94885C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40654549 | ||||||
| chr7:40657509
|
A | AT | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.1090-91916dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40657509 | |||||
| chr7:40657804
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1090-91630A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40657804 | ||||||
| chr7:40658283
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-91151T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40658283 | ||||||
| chr7:40658338
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-91096T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40658338 | ||||||
| chr7:40659290
|
T | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-90144T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40659290 | ||||||
| chr7:40659308
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-90126A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40659308 | ||||||
| chr7:40659590
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-89844G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40659590 | ||||||
| chr7:40660503
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-88931C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40660503 | ||||||
| chr7:40660671
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1090-88763G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40660671 | ||||||
| chr7:40660901
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-88533A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40660901 | ||||||
| chr7:40661018
|
A | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-88416A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40661018 | ||||||
| chr7:40661034
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-88400A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40661034 | ||||||
| chr7:40661303
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-88131C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40661303 | ||||||
| chr7:40661754
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090-87680T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40661754 | ||||||
| chr7:40662060
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-87374G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40662060 | ||||||
| chr7:40662109
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-87325G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40662109 | ||||||
| chr7:40662124
|
C | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-87310C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40662124 | ||||||
| chr7:40662726
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-86708G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40662726 | ||||||
| chr7:40662904
|
C | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1090-86530C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40662904 | ||||||
| chr7:40663296
|
CA | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.1090-86128delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40663296 | |||||
| chr7:40663519
|
G | GTGTGTA | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-85912_1090-85 others(12): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40663519 | |||||
| chr7:40663690
|
G | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-85744G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40663690 | ||||||
| chr7:40663941
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-85493A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40663941 | ||||||
| chr7:40664979
|
CAAA | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-84439_1090-84 others(9): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40664979 | |||||
| chr7:40665093
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-84341T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40665093 | ||||||
| chr7:40665267
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.1090-84167T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40665267 | ||||||
| chr7:40665547
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-83887G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40665547 | ||||||
| chr7:40666306
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-83128C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40666306 | ||||||
| chr7:40666350
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1090-83084G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40666350 | ||||||
| chr7:40666355
|
A | AAAGAAAG others(5): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-83076_1090-83 others(18): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40666355 | |||||
| chr7:40666355
|
A | AAAGAAAG others(21): Show |
1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-83076_1090-83 others(34): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40666355 | |||||
| chr7:40666355
|
A | AAAGGAAG others(9): Show |
1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-83056_1090-83 others(22): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40666355 | |||||
| chr7:40666355
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1090-83079A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40666355 | ||||||
| chr7:40666419
|
G | GT | 3 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0003t0001g0005 | 3 | HG00738.hp1 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1090-82990dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40666419 | |||||
| chr7:40666419
|
G | GTTTT | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-82993_1090-82 others(10): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40666419 | |||||
| chr7:40667019
|
G | C | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1090-82415G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40667019 | ||||||
| chr7:40667026
|
G | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-82408G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40667026 | ||||||
| chr7:40667251
|
TTA | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-82181_1090-82 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40667251 | |||||
| chr7:40667578
|
CT | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-81842delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40667578 | |||||
| chr7:40667734
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-81700C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40667734 | ||||||
| chr7:40668634
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-80800A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40668634 | ||||||
| chr7:40669295
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-80139T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40669295 | ||||||
| chr7:40669346
|
CAAAAAA | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-80070_1090-80 others(12): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40669346 | |||||
| chr7:40670169
|
CA | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-79241delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40670169 | |||||
| chr7:40670498
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-78936G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40670498 | ||||||
| chr7:40670669
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1090-78765A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40670669 | ||||||
| chr7:40670721
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-78713A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40670721 | ||||||
| chr7:40671144
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-78290C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40671144 | ||||||
| chr7:40671344
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-78090G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40671344 | ||||||
| chr7:40671367
|
C | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-78067C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40671367 | ||||||
| chr7:40672780
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-76654C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40672780 | ||||||
| chr7:40676137
|
G | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-73297G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40676137 | ||||||
| chr7:40676382
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-73052G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40676382 | ||||||
| chr7:40676504
|
G | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-72930G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40676504 | ||||||
| chr7:40676894
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-72508_1090-72 others(16): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40676894 | |||||
| chr7:40676894
|
CGTGT | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0003t0001g0005 | 3 | HG01069.hp1 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1090-72502_1090-72 others(10): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40676894 | |||||
| chr7:40677102
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-72332A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40677102 | ||||||
| chr7:40677627
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-71807C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40677627 | ||||||
| chr7:40678037
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-71397C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40678037 | ||||||
| chr7:40678412
|
T | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-71022T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40678412 | ||||||
| chr7:40679271
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1090-70163T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40679271 | ||||||
| chr7:40680048
|
A | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-69386A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40680048 | ||||||
| chr7:40680808
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-68626A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40680808 | ||||||
| chr7:40682842
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-66592T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40682842 | ||||||
| chr7:40683321
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-66113G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40683321 | ||||||
| chr7:40683658
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-65776T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40683658 | ||||||
| chr7:40683767
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-65667C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40683767 | ||||||
| chr7:40684533
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-64901C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40684533 | ||||||
| chr7:40684756
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-64678G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40684756 | ||||||
| chr7:40684840
|
T | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-64594T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40684840 | ||||||
| chr7:40685399
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-64035C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40685399 | ||||||
| chr7:40685902
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-63532T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40685902 | ||||||
| chr7:40686391
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-63043G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40686391 | ||||||
| chr7:40686608
|
C | CT | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-62821dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40686608 | |||||
| chr7:40686705
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-62729G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40686705 | ||||||
| chr7:40687624
|
T | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-61810T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40687624 | ||||||
| chr7:40689011
|
G | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-60423G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40689011 | ||||||
| chr7:40689269
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-60165A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40689269 | ||||||
| chr7:40689333
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-60101A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40689333 | ||||||
| chr7:40690327
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-59107G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40690327 | ||||||
| chr7:40690740
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-58694C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40690740 | ||||||
| chr7:40690998
|
G | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.1090-58436G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40690998 | ||||||
| chr7:40691004
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-58430T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40691004 | ||||||
| chr7:40691662
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-57772T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40691662 | ||||||
| chr7:40691805
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-57629T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40691805 | ||||||
| chr7:40691979
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-57455G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40691979 | ||||||
| chr7:40692095
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-57339C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40692095 | ||||||
| chr7:40692288
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-57146A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40692288 | ||||||
| chr7:40692750
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-56684A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40692750 | ||||||
| chr7:40692833
|
CA | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-56600delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40692833 | ||||||
| chr7:40693142
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-56292C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40693142 | ||||||
| chr7:40693385
|
G | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-56049G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40693385 | ||||||
| chr7:40693602
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1090-55832C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40693602 | ||||||
| chr7:40694157
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-55277C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40694157 | ||||||
| chr7:40695167
|
T | TTTTA | 4 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(1): Show | 4 | HG00738.hp1 HG00738.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1090-54219_1090-54 others(10): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40695167 | |||||
| chr7:40695167
|
T | TTTTATTT others(1): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-54223_1090-54 others(14): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40695167 | |||||
| chr7:40696715
|
G | A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1090-52719G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40696715 | ||||||
| chr7:40698217
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-51217A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40698217 | ||||||
| chr7:40698977
|
T | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-50457T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40698977 | ||||||
| chr7:40699684
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-49750T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40699684 | ||||||
| chr7:40699686
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-49748C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40699686 | ||||||
| chr7:40700000
|
C | CT | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-49430dupT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40700000 | |||||
| chr7:40700701
|
T | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-48733T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40700701 | ||||||
| chr7:40701813
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-47621A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40701813 | ||||||
| chr7:40703061
|
CTT | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-46354_1090-46 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40703061 | |||||
| chr7:40703087
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-46347A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40703087 | ||||||
| chr7:40703944
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-45490C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40703944 | ||||||
| chr7:40704115
|
T | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-45319T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40704115 | ||||||
| chr7:40704212
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-45222T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40704212 | ||||||
| chr7:40705075
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-44359G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40705075 | ||||||
| chr7:40705522
|
C | CT | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-43912_1090-43 others(7): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40705522 | ||||||
| chr7:40706151
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-43283A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40706151 | ||||||
| chr7:40706272
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-43162C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40706272 | ||||||
| chr7:40707249
|
T | A | 2 | a0001c0001t0001g0002a0001c0003t0001g0005 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1090-42185T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40707249 | ||||||
| chr7:40707249
|
T | TA | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.1090-42180dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40707249 | |||||
| chr7:40709051
|
A | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090-40383A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40709051 | ||||||
| chr7:40709595
|
T | A | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1090-39839T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40709595 | ||||||
| chr7:40709910
|
G | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-39524G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40709910 | ||||||
| chr7:40710154
|
G | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-39280G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40710154 | ||||||
| chr7:40710531
|
T | G | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1090-38903T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40710531 | ||||||
| chr7:40711798
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-37636T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40711798 | ||||||
| chr7:40712460
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-36974G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40712460 | ||||||
| chr7:40712767
|
C | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-36667C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40712767 | ||||||
| chr7:40713832
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0003t0001g0005 | 3 | HG00738.hp1 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1090-35602T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40713832 | ||||||
| chr7:40714027
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0003t0001g0005 | 3 | HG00738.hp1 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1090-35407T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40714027 | ||||||
| chr7:40714416
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-35018C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40714416 | ||||||
| chr7:40715349
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090-34085C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40715349 | ||||||
| chr7:40715547
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090-33887C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40715547 | ||||||
| chr7:40715930
|
C | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-33504C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40715930 | ||||||
| chr7:40716127
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-33307A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40716127 | ||||||
| chr7:40716379
|
C | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0004 | 2 | HG00738.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1090-33055C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40716379 | ||||||
| chr7:40716896
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-32538A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40716896 | ||||||
| chr7:40717300
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1090-32134T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40717300 | ||||||
| chr7:40717324
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090-32110C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40717324 | ||||||
| chr7:40717419
|
G | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-32015G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40717419 | ||||||
| chr7:40717894
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-31540A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40717894 | ||||||
| chr7:40717920
|
TCTC | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-31510_1090-31 others(9): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40717920 | |||||
| chr7:40717924
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-31510C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40717924 | ||||||
| chr7:40718068
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090-31366G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40718068 | ||||||
| chr7:40718094
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp2 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-31340G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40718094 | ||||||
| chr7:40718292
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-31142C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40718292 | ||||||
| chr7:40718542
|
T | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-30892T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40718542 | ||||||
| chr7:40718601
|
T | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090-30833T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40718601 | ||||||
| chr7:40719751
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-29683C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40719751 | ||||||
| chr7:40720071
|
G | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-29363G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40720071 | ||||||
| chr7:40720131
|
T | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-29303T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40720131 | ||||||
| chr7:40720788
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-28646C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40720788 | ||||||
| chr7:40720899
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-28535A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40720899 | ||||||
| chr7:40720907
|
A | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-28527A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40720907 | ||||||
| chr7:40721224
|
A | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-28210A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40721224 | ||||||
| chr7:40721275
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-28159G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40721275 | ||||||
| chr7:40721544
|
C | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-27890C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40721544 | ||||||
| chr7:40721879
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1090-27555A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40721879 | ||||||
| chr7:40722066
|
A | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-27368A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40722066 | ||||||
| chr7:40723117
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-26317G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40723117 | ||||||
| chr7:40723325
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-26109A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40723325 | ||||||
| chr7:40724420
|
C | CAG | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-25014_1090-25 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40724420 | ||||||
| chr7:40724480
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-24954A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40724480 | ||||||
| chr7:40724574
|
C | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-24860C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40724574 | ||||||
| chr7:40725396
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-24038C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40725396 | ||||||
| chr7:40726165
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-23269G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40726165 | ||||||
| chr7:40726542
|
T | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-22892T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40726542 | ||||||
| chr7:40726850
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-22584G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40726850 | ||||||
| chr7:40727016
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-22418T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40727016 | ||||||
| chr7:40727368
|
C | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-22066C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40727368 | ||||||
| chr7:40728833
|
T | A | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1090-20601T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40728833 | ||||||
| chr7:40729140
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-20294A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40729140 | ||||||
| chr7:40730425
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-19009A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40730425 | ||||||
| chr7:40730879
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-18555A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40730879 | ||||||
| chr7:40731466
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-17968C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40731466 | ||||||
| chr7:40731996
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1090-17438A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40731996 | ||||||
| chr7:40732449
|
T | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-16985T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40732449 | ||||||
| chr7:40732842
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-16592C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40732842 | ||||||
| chr7:40732926
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-16508C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40732926 | ||||||
| chr7:40732955
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-16479A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40732955 | ||||||
| chr7:40733992
|
A | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-15442A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40733992 | ||||||
| chr7:40734005
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-15429T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40734005 | ||||||
| chr7:40734706
|
T | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-14728T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40734706 | ||||||
| chr7:40734825
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1090-14609T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40734825 | ||||||
| chr7:40734995
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-14439G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40734995 | ||||||
| chr7:40735338
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-14096G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40735338 | ||||||
| chr7:40736117
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-13317G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40736117 | ||||||
| chr7:40736229
|
ATCAATAT others(25): Show |
A | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-13171_1090-13 others(38): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 40736229 | |||||
| chr7:40736392
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-13042G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40736392 | ||||||
| chr7:40736829
|
G | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp2 HG01192.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-12605G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40736829 | ||||||
| chr7:40737947
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-11487G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40737947 | ||||||
| chr7:40737953
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1090-11481A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40737953 | ||||||
| chr7:40739233
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-10201C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40739233 | ||||||
| chr7:40739368
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1090-10066G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40739368 | ||||||
| chr7:40739627
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-9807C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40739627 | ||||||
| chr7:40740166
|
T | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-9268T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40740166 | ||||||
| chr7:40740541
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-8893T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40740541 | ||||||
| chr7:40741388
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1090-8046C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40741388 | ||||||
| chr7:40742425
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00738.hp1 HG01069.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-7009A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40742425 | ||||||
| chr7:40742633
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-6801C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40742633 | ||||||
| chr7:40742973
|
T | C | 2 | a0001c0001t0001g0003a0001c0002t0001g0001 | 2 | HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1090-6461T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40742973 | ||||||
| chr7:40747333
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1090-2101C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40747333 | ||||||
| chr7:40747505
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-1929T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40747505 | ||||||
| chr7:40748482
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1090-952A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 12/13 | chr7 | 40748482 | ||||||
| chr7:40750295
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+798G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40750295 | ||||||
| chr7:40750658
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+1161A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40750658 | ||||||
| chr7:40750783
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1153+1286A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40750783 | ||||||
| chr7:40751941
|
C | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+2444C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40751941 | ||||||
| chr7:40752405
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+2908A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40752405 | ||||||
| chr7:40753492
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1153+3995G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40753492 | ||||||
| chr7:40753959
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+4462G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40753959 | ||||||
| chr7:40754097
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+4600G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40754097 | ||||||
| chr7:40754121
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1153+4624A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40754121 | ||||||
| chr7:40754926
|
A | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+5429A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40754926 | ||||||
| chr7:40755513
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1153+6016A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40755513 | ||||||
| chr7:40755601
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1153+6104A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40755601 | ||||||
| chr7:40756871
|
A | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+7374A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40756871 | ||||||
| chr7:40757019
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+7522G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40757019 | ||||||
| chr7:40757137
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+7640G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40757137 | ||||||
| chr7:40757620
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+8123C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40757620 | ||||||
| chr7:40757849
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1153+8352G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40757849 | ||||||
| chr7:40758668
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.1153+9171C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40758668 | ||||||
| chr7:40759573
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+10076G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40759573 | ||||||
| chr7:40760453
|
C | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+10956C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40760453 | ||||||
| chr7:40762273
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+12776G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40762273 | ||||||
| chr7:40763261
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1153+13764A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40763261 | ||||||
| chr7:40764636
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1153+15139G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40764636 | ||||||
| chr7:40764796
|
C | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+15299C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40764796 | ||||||
| chr7:40764889
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+15392G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40764889 | ||||||
| chr7:40765466
|
G | GA | 3 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG00738.hp1 HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1153+15980dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40765466 | |||||
| chr7:40765604
|
A | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+16107A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40765604 | ||||||
| chr7:40765716
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1153+16219C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40765716 | ||||||
| chr7:40766098
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+16601C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40766098 | ||||||
| chr7:40766995
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1153+17498G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40766995 | ||||||
| chr7:40767859
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+18362A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40767859 | ||||||
| chr7:40769098
|
T | TA | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01069.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1153+19610dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40769098 | |||||
| chr7:40769544
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+20047G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40769544 | ||||||
| chr7:40770802
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+21305A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40770802 | ||||||
| chr7:40772480
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+22983T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40772480 | ||||||
| chr7:40772494
|
ATATC | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0003t0001g0005 | 3 | HG01069.hp2 HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1153+23063_1153+23 others(10): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40772494 | |||||
| chr7:40772494
|
ATATCTAT others(1): Show |
A | 2 | a0001c0001t0001g0002a0001c0001t0001g0004 | 2 | HG00738.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1153+23059_1153+23 others(14): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40772494 | |||||
| chr7:40772494
|
ATATCTAT others(5): Show |
A | 2 | a0001c0001t0001g0006a0001c0002t0001g0001 | 2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+23055_1153+23 others(18): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40772494 | |||||
| chr7:40772578
|
G | GCTAT | 5 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp2 HG01069.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153+23132_1153+23 others(10): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40772578 | |||||
| chr7:40774777
|
TA | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+25295delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40774777 | |||||
| chr7:40775426
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+25929A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40775426 | ||||||
| chr7:40776296
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+26799G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40776296 | ||||||
| chr7:40776840
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+27343T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40776840 | ||||||
| chr7:40776866
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+27369C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40776866 | ||||||
| chr7:40777463
|
T | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+27966T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40777463 | ||||||
| chr7:40778237
|
C | CTT | 4 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+28741_1153+28 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40778237 | |||||
| chr7:40779369
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1153+29872C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40779369 | ||||||
| chr7:40779479
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1153+29982G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40779479 | ||||||
| chr7:40780775
|
CT | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+31293delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40780775 | |||||
| chr7:40782522
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+33025T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40782522 | ||||||
| chr7:40782715
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+33218G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40782715 | ||||||
| chr7:40783235
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+33738T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40783235 | ||||||
| chr7:40785957
|
A | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+36460A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40785957 | ||||||
| chr7:40786209
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+36712G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40786209 | ||||||
| chr7:40786442
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+36945C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40786442 | ||||||
| chr7:40786672
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+37175G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40786672 | ||||||
| chr7:40786675
|
A | C | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1153+37178A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40786675 | ||||||
| chr7:40786721
|
A | AC | 4 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+37229dupC | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40786721 | |||||
| chr7:40786736
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1153+37239A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40786736 | ||||||
| chr7:40786789
|
A | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+37292A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40786789 | ||||||
| chr7:40787163
|
G | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+37666G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40787163 | ||||||
| chr7:40787458
|
CAAGATCT others(11): Show |
C | 4 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+37981_1153+37 others(24): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40787458 | |||||
| chr7:40787660
|
C | CA | 4 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(1): Show | 4 | HG00738.hp1 HG00738.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+38187dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40787660 | |||||
| chr7:40788052
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+38555C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40788052 | ||||||
| chr7:40788156
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+38659T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40788156 | ||||||
| chr7:40788363
|
A | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+38866A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40788363 | ||||||
| chr7:40789845
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+40348G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40789845 | ||||||
| chr7:40789887
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+40390G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40789887 | ||||||
| chr7:40790514
|
A | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+41017A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40790514 | ||||||
| chr7:40791238
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+41741T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40791238 | ||||||
| chr7:40791436
|
C | CCATT | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+41939_1153+41 others(10): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40791436 | ||||||
| chr7:40791697
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+42200G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40791697 | ||||||
| chr7:40792545
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+43048C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40792545 | ||||||
| chr7:40792998
|
A | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+43501A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40792998 | ||||||
| chr7:40794001
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+44504G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40794001 | ||||||
| chr7:40794018
|
AT | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+44529delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40794018 | |||||
| chr7:40795117
|
T | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+45620T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40795117 | ||||||
| chr7:40795225
|
T | TA | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+45732dupA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40795225 | |||||
| chr7:40796346
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+46849T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40796346 | ||||||
| chr7:40796620
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+47123A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40796620 | ||||||
| chr7:40796645
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+47148A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40796645 | ||||||
| chr7:40796692
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+47195T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40796692 | ||||||
| chr7:40796922
|
G | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+47425G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40796922 | ||||||
| chr7:40797715
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+48218A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40797715 | ||||||
| chr7:40797903
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1153+48406G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40797903 | ||||||
| chr7:40798137
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+48640A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40798137 | ||||||
| chr7:40798138
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+48641T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40798138 | ||||||
| chr7:40798746
|
GAT | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+49254_1153+49 others(8): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40798746 | |||||
| chr7:40798961
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+49464T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40798961 | ||||||
| chr7:40799358
|
C | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+49861C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40799358 | ||||||
| chr7:40800048
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+50551C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40800048 | ||||||
| chr7:40800286
|
CT | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+50808delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40800286 | |||||
| chr7:40800557
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+51060A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40800557 | ||||||
| chr7:40801371
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+51874C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40801371 | ||||||
| chr7:40801440
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+51943C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40801440 | ||||||
| chr7:40801973
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+52476A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40801973 | ||||||
| chr7:40802379
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+52882A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40802379 | ||||||
| chr7:40802546
|
A | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+53049A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40802546 | ||||||
| chr7:40802693
|
C | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.1153+53196C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40802693 | ||||||
| chr7:40802738
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(2): Show | 5 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+53241T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40802738 | ||||||
| chr7:40804571
|
GA | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+55087delA | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40804571 | |||||
| chr7:40804864
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1153+55367G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40804864 | ||||||
| chr7:40806203
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-54113C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40806203 | ||||||
| chr7:40806492
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-53824T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40806492 | ||||||
| chr7:40807622
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-52694C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40807622 | ||||||
| chr7:40808049
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-52267G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40808049 | ||||||
| chr7:40808233
|
A | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(2): Show | 5 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154-52083A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40808233 | ||||||
| chr7:40808310
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-52006G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40808310 | ||||||
| chr7:40808607
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-51709T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40808607 | ||||||
| chr7:40808804
|
G | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-51512G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40808804 | ||||||
| chr7:40811191
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-49125C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40811191 | ||||||
| chr7:40811454
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-48862T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40811454 | ||||||
| chr7:40811521
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-48795G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40811521 | ||||||
| chr7:40811567
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-48749C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40811567 | ||||||
| chr7:40811643
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-48673G>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40811643 | ||||||
| chr7:40812136
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-48180T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40812136 | ||||||
| chr7:40812323
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-47993A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40812323 | ||||||
| chr7:40813034
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-47282G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40813034 | ||||||
| chr7:40813904
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-46412A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40813904 | ||||||
| chr7:40814705
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-45611C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40814705 | ||||||
| chr7:40816121
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-44195A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40816121 | ||||||
| chr7:40816883
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-43433C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40816883 | ||||||
| chr7:40817249
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-43067C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40817249 | ||||||
| chr7:40817522
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-42794T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40817522 | ||||||
| chr7:40818979
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-41337C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40818979 | ||||||
| chr7:40820280
|
GT | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-40029delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40820280 | |||||
| chr7:40820933
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-39383G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40820933 | ||||||
| chr7:40821093
|
C | G | 1 | a0001c0001t0001g0006 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1154-39223C>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40821093 | ||||||
| chr7:40821485
|
A | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-38831A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40821485 | ||||||
| chr7:40822230
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-38086T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40822230 | ||||||
| chr7:40823164
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-37152T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40823164 | ||||||
| chr7:40823928
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1154-36388C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40823928 | ||||||
| chr7:40825620
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-34696T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40825620 | ||||||
| chr7:40825704
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-34612C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40825704 | ||||||
| chr7:40825984
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-34332G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40825984 | ||||||
| chr7:40826097
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-34219C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40826097 | ||||||
| chr7:40826636
|
T | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-33680T>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40826636 | ||||||
| chr7:40826643
|
G | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-33673G>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40826643 | ||||||
| chr7:40827064
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-33252C>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40827064 | ||||||
| chr7:40830155
|
A | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-30161A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40830155 | ||||||
| chr7:40831336
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154-28980A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40831336 | ||||||
| chr7:40831787
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1154-28529A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40831787 | ||||||
| chr7:40832259
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-28057A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40832259 | ||||||
| chr7:40833622
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-26694A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40833622 | ||||||
| chr7:40835593
|
A | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-24723A>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40835593 | ||||||
| chr7:40837874
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0002t0001g0001 | 3 | HG00738.hp2 HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1154-22442A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40837874 | ||||||
| chr7:40838120
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1154-22196G>A | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40838120 | ||||||
| chr7:40839216
|
T | G | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1154-21100T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40839216 | ||||||
| chr7:40843277
|
C | T | 1 | a0001c0002t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1154-17039C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40843277 | ||||||
| chr7:40845020
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1154-15296A>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40845020 | ||||||
| chr7:40847411
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1154-12905C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | chr7 | 40847411 | ||||||
| chr7:40847411
|
CT | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(1): Show | 4 | HG00738.hp1 HG00738.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-12882delT | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40847411 | |||||
| chr7:40854419
|
C | CCTTTCTT others(5): Show |
2 | a0001c0001t0001g0002a0001c0003t0001g0005 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1154-5850_1154-583 others(16): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40854419 | |||||
| chr7:40854419
|
C | CCTTTCTT others(9): Show |
1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1154-5854_1154-583 others(20): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40854419 | |||||
| chr7:40854419
|
C | CCTTTCTT others(13): Show |
2 | a0001c0001t0001g0003a0001c0001t0001g0007 | 2 | HG01069.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1154-5858_1154-583 others(24): Show |
SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 40854419 |