Item | Value |
---|---|
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 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1314 | 6 | 1 | 5 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | ATGCT others(1309): Show |
chr7 | 40130005 | 40865763 | ||
a0001c0002 | 0/0 | 1314 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | ATGCT others(1309): Show |
chr7 | 40130005 | 40865763 | ||
a0001c0003 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | ATGCT others(1309): Show |
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 | ATCTG others(1612): Show |
chr7 | 40130005 | 40865763 |
a0001c0002t0001 | 0/0 | 1617 | 1 | 0 | 1 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | ATCTG others(1612): Show |
chr7 | 40130005 | 40865763 |
a0001c0003t0001 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | SUGCT_chr7_40130005_40865763 | SUGCT | ATCTG others(1612): Show |
chr7 | 40130005 | 40865763 |
actghapid | grch38/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 |
view | 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 |
---|
view | 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 |
view | 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 |
---|
view | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | |||||||
chr7:40138769 | T | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | |||||||
chr7:40242931 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+6841T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40244567 | |||||||
chr7:40245404 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0007 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | |||||||
chr7:40246251 | C | CT | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | |||||||
chr7:40248262 | G | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
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 | ||||||
chr7:40249563 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
2 | HG00738.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.576+13189C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40250915 | |||||||
chr7:40251380 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.577-15901C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40258612 | |||||||
chr7:40259279 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | |||||||
chr7:40265463 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
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 | ||||||
chr7:40266218 | C | T | 2 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | |||||||
chr7:40267025 | A | AAAAC | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | |||||||
chr7:40272141 | C | CATATAT | 2 | a0001c0001t0001g0007 a0001c0003t0001g0005 |
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 | ||||||
chr7:40272191 | 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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
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 | ||||||
chr7:40273710 | T | C | 2 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.577-803T>C | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 7/13 | chr7 | 40273710 | |||||||
chr7:40276817 | GTGTC | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | |||||||
chr7:40277316 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | ||||||
chr7:40277677 | G | GTTATTA | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | ||||||
chr7:40278385 | 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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
2 | HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.720+3933T>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40278589 | |||||||
chr7:40279022 | T | TG | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | ||||||
chr7:40279927 | 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 | |||||||
chr7:40280296 | 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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
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 | ||||||
chr7:40281758 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | |||||||
chr7:40282492 | AAAAC | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | ||||||
chr7:40283145 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | |||||||
chr7:40286332 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | |||||||
chr7:40287500 | C | CT | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | ||||||
chr7:40288316 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | |||||||
chr7:40290941 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | |||||||
chr7:40291032 | T | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | |||||||
chr7:40291672 | A | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | |||||||
chr7:40294343 | T | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | ||||||
chr7:40297339 | 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 | |||||||
chr7:40298772 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | ||||||
chr7:40300587 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.721-14471C>T | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40302289 | |||||||
chr7:40302419 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.721-13497A>G | SUGCT | ENSG00000175600.16 | transcript | ENST00000335693.9 | protein_coding | 8/13 | chr7 | 40303263 | |||||||
chr7:40304759 | AATC | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0002t0001g0001 a0001c0003t0001g0005 |
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 | ||||||
chr7:40310106 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | |||||||
chr7:40313632 | TTTTTG | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | |||||||
chr7:40314114 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | |||||||
chr7:40318541 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | |||||||
chr7:40318886 | A | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0004 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0002t0001g0001 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | |||||||
chr7:40327291 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0004 a0001c0002t0001g0001 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | ||||||
chr7:40376746 | C | CT | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 |
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 | a0001c0002t0001g0001 a0001c0003t0001g0005 |
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 | a0001c0002t0001g0001 a0001c0003t0001g0005 |
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 | a0001c0002t0001g0001 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0002t0001g0001 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | |||||||
chr7:40397025 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0004 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | ||||||
chr7:40428692 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | |||||||
chr7:40438379 | 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 | a0001c0002t0001g0001 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0002t0001g0001 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0002t0001g0001 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | |||||||
chr7:40470747 | G | GTCTC | 2 | a0001c0001t0001g0004 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | |||||||
chr7:40500884 | AACACAT | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | |||||||
chr7:40547075 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0003 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | |||||||
chr7:40593862 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | |||||||
chr7:40614163 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0006 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0006 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | |||||||
chr7:40665547 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | |||||||
chr7:40691004 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0002 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | |||||||
chr7:40759573 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0003t0001g0005 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | |||||||
chr7:40802738 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0002t0001g0001 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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(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 | a0001c0001t0001g0003 a0001c0001t0001g0007 |
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 |