Item | Value |
---|---|
geneid | 26173 |
ensemblid | ENSG00000164880.16 |
hgncid | 24555 |
symbol | INTS1 |
name | integrator complex subunit 1 |
refseq_nuc | NM_001080453.3 |
refseq_prot | NP_001073922.2 |
ensembl_nuc | ENST00000404767.8 |
ensembl_prot | ENSP00000385722.3 |
mane_status | MANE Select |
chr | chr7 |
start | 1470277 |
end | 1504389 |
strand | - |
ver | v1.2 |
region | chr7:1470277-1504389 |
region5000 | chr7:1465277-1509389 |
regionname0 | INTS1_chr7_1470277_1504389 |
regionname5000 | INTS1_chr7_1465277_1509389 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2190 | 294 | 81 | 66 | 103 | 14 | 28 | 63 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0002 | 0/0 | 2190 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0003 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0004 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0005 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0006 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0007 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0008 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2170): Show |
chr7 | 1465277 | 1509389 |
a0009 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0010 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0011 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0012 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | MNRTK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0013 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0014 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0015 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0016 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0017 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0018 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
a0019 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | MNRAK others(2185): Show |
chr7 | 1465277 | 1509389 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 6570 | 129 | 32 | 22 | 57 | 8 | 9 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0002 | 1/0 | 6570 | 103 | 14 | 34 | 37 | 4 | 13 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0003 | 0/0 | 6570 | 8 | 6 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0004 | 0/0 | 6570 | 7 | 1 | 0 | 6 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0005 | 0/0 | 6570 | 6 | 4 | 1 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0006 | 0/0 | 6570 | 4 | 3 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0008 | 0/0 | 6570 | 3 | 0 | 0 | 0 | 0 | 3 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0009 | 0/0 | 6570 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0010 | 0/0 | 6570 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0011 | 0/0 | 6570 | 3 | 1 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0012 | 0/0 | 6570 | 2 | 0 | 0 | 0 | 0 | 2 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0013 | 0/0 | 6570 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0016 | 0/0 | 6570 | 2 | 0 | 1 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0018 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0019 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0020 | 0/0 | 6570 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0021 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0022 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0023 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0028 | 0/0 | 6570 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0031 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0034 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0035 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0036 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0037 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0038 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0039 | 0/0 | 6570 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0041 | 0/0 | 6570 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0042 | 0/0 | 6570 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0047 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0048 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0001c0049 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0002c0007 | 0/0 | 6570 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0003c0015 | 0/0 | 6570 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0004c0014 | 0/0 | 6570 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0005c0029 | 0/0 | 6570 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0006c0027 | 0/0 | 6570 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0007c0024 | 0/0 | 6570 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0008c0032 | 0/0 | 6525 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6520): Show |
chr7 | 1465277 | 1509389 | ||
a0009c0033 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0010c0026 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0011c0025 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0012c0017 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0013c0046 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0014c0044 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0015c0045 | 0/0 | 6570 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0016c0030 | 0/0 | 6570 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0017c0050 | 0/0 | 6570 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0018c0040 | 0/0 | 6570 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 | ||
a0019c0043 | 0/0 | 6570 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | ATGAA others(6565): Show |
chr7 | 1465277 | 1509389 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6981 | 118 | 30 | 22 | 49 | 7 | 9 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0001t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0001t0003 | 0/0 | 6981 | 7 | 0 | 0 | 7 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0001t0006 | 0/0 | 6982 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6977): Show |
chr7 | 1465277 | 1509389 |
a0001c0001t0011 | 0/0 | 6981 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0001t0014 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GTGTT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0002t0002 | 1/0 | 6981 | 101 | 14 | 32 | 37 | 4 | 13 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0002t0008 | 0/0 | 6981 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0002t0009 | 0/0 | 6981 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0003t0001 | 0/0 | 6981 | 8 | 6 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0004t0001 | 0/0 | 6981 | 7 | 1 | 0 | 6 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0005t0001 | 0/0 | 6981 | 6 | 4 | 1 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0006t0005 | 0/0 | 6978 | 4 | 3 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6973): Show |
chr7 | 1465277 | 1509389 |
a0001c0008t0004 | 0/0 | 6981 | 2 | 0 | 0 | 0 | 0 | 2 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0008t0007 | 0/0 | 6982 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6977): Show |
chr7 | 1465277 | 1509389 |
a0001c0009t0001 | 0/0 | 6981 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0010t0001 | 0/0 | 6981 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0011t0001 | 0/0 | 6981 | 3 | 1 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0012t0001 | 0/0 | 6981 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0012t0002 | 0/0 | 6981 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0013t0002 | 0/0 | 6981 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0016t0001 | 0/0 | 6981 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0016t0013 | 0/0 | 6981 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0018t0004 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0019t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0020t0002 | 0/0 | 6981 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0021t0004 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0022t0004 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0023t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0028t0002 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0031t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0034t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0035t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0036t0012 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6973): Show |
chr7 | 1465277 | 1509389 |
a0001c0037t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0038t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0039t0001 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0041t0006 | 0/0 | 6982 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6977): Show |
chr7 | 1465277 | 1509389 |
a0001c0042t0001 | 0/0 | 6981 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0047t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0048t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0001c0049t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0002c0007t0004 | 0/0 | 6981 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0003c0015t0001 | 0/0 | 6981 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0004c0014t0002 | 0/0 | 6981 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0005c0029t0002 | 0/0 | 6981 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0006c0027t0002 | 0/0 | 6981 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0007c0024t0002 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0008c0032t0003 | 0/0 | 6936 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6931): Show |
chr7 | 1465277 | 1509389 |
a0009c0033t0010 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0010c0026t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0011c0025t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0012c0017t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0013c0046t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0014c0044t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0015c0045t0001 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0016c0030t0001 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0017c0050t0001 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0018c0040t0003 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
a0019c0043t0001 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | GAGAT others(6976): Show |
chr7 | 1465277 | 1509389 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0011g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0014g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0002 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0003 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0004 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0008g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0009g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0003t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0003t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0004t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0005t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0005t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0005t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0005t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0006t0005g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0006t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0006t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0008t0004g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0008t0007g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0009t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0009t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0010t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0010t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0011t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0011t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0012t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0012t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0013t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0016t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0016t0013g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0018t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0019t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0020t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0021t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0022t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0023t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0028t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0031t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0034t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0035t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0036t0012g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0037t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0038t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0039t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0041t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0042t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0047t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0048t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0049t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0002c0007t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0002c0007t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0003c0015t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0004c0014t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0004c0014t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0005c0029t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0006c0027t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0007c0024t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0008c0032t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0009c0033t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0010c0026t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0011c0025t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0012c0017t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0013c0046t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0014c0044t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0015c0045t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0016c0030t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0017c0050t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0018c0040t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0019c0043t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0004 | EUR | GBR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00280 | hp2 | a0001 | c0005 | t0001 | g0139 | EUR | FIN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00408 | hp2 | a0001 | c0004 | t0001 | g0017 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00639 | hp1 | a0001 | c0011 | t0001 | g0040 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00642 | hp2 | a0005 | c0029 | t0002 | g0098 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00735 | hp2 | a0001 | c0002 | t0009 | g0101 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01074 | hp1 | a0001 | c0016 | t0001 | g0162 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01081 | hp2 | a0001 | c0011 | t0001 | g0040 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0100 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01109 | hp2 | a0001 | c0020 | t0002 | g0104 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0062 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01175 | hp2 | a0001 | c0005 | t0001 | g0138 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01243 | hp1 | a0001 | c0006 | t0005 | g0226 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0197 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0039 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01257 | hp2 | a0001 | c0013 | t0002 | g0023 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01258 | hp2 | a0001 | c0013 | t0002 | g0023 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0087 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0088 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01516 | hp2 | a0001 | c0001 | t0011 | g0155 | EUR | IBS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01884 | hp1 | a0001 | c0005 | t0001 | g0212 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01943 | hp1 | a0001 | c0002 | t0008 | g0067 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01952 | hp1 | a0006 | c0027 | t0002 | g0084 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0083 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0052 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0056 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02040 | hp2 | a0007 | c0024 | t0002 | g0063 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02056 | hp2 | a0008 | c0032 | t0003 | g0190 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02129 | hp1 | a0001 | c0004 | t0001 | g0017 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02145 | hp2 | a0009 | c0033 | t0010 | g0119 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | CDX | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CDX | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0195 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02258 | hp2 | a0001 | c0023 | t0002 | g0091 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02280 | hp1 | a0001 | c0010 | t0001 | g0031 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02280 | hp2 | a0001 | c0018 | t0004 | g0109 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02451 | hp1 | a0010 | c0026 | t0002 | g0068 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02451 | hp2 | a0001 | c0010 | t0001 | g0144 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02572 | hp1 | a0001 | c0006 | t0005 | g0225 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0041 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0095 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02630 | hp1 | a0001 | c0006 | t0005 | g0043 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02647 | hp1 | a0011 | c0025 | t0002 | g0089 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02647 | hp2 | a0001 | c0047 | t0001 | g0176 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02698 | hp1 | a0001 | c0042 | t0001 | g0202 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0072 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02717 | hp1 | a0001 | c0006 | t0005 | g0043 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02717 | hp2 | a0001 | c0048 | t0001 | g0189 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02723 | hp1 | a0002 | c0007 | t0004 | g0028 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02738 | hp1 | a0001 | c0008 | t0004 | g0019 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02738 | hp2 | a0001 | c0012 | t0001 | g0118 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0041 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02886 | hp1 | a0012 | c0017 | t0001 | g0115 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02886 | hp2 | a0001 | c0035 | t0001 | g0142 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02895 | hp1 | a0001 | c0009 | t0001 | g0042 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02897 | hp1 | a0001 | c0005 | t0001 | g0117 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02922 | hp2 | a0001 | c0005 | t0001 | g0213 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0060 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03041 | hp1 | a0001 | c0036 | t0012 | g0224 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03041 | hp2 | a0003 | c0015 | t0001 | g0036 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03098 | hp1 | a0001 | c0022 | t0004 | g0111 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03130 | hp1 | a0001 | c0009 | t0001 | g0042 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03130 | hp2 | a0002 | c0007 | t0004 | g0108 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03139 | hp1 | a0001 | c0049 | t0002 | g0107 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03139 | hp2 | a0003 | c0015 | t0001 | g0036 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0090 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0046 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03225 | hp1 | a0001 | c0011 | t0001 | g0208 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0039 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0079 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03453 | hp1 | a0013 | c0046 | t0001 | g0175 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03453 | hp2 | a0001 | c0031 | t0001 | g0124 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03486 | hp2 | a0001 | c0038 | t0001 | g0116 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0049 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03492 | hp2 | a0001 | c0008 | t0004 | g0019 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03540 | hp2 | a0001 | c0037 | t0001 | g0196 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0070 | SAS | STU | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03831 | hp1 | a0001 | c0008 | t0007 | g0044 | SAS | BEB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG04184 | hp1 | a0001 | c0012 | t0002 | g0057 | SAS | BEB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0048 | SAS | STU | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0073 | SAS | STU | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | YRI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18522 | hp2 | a0014 | c0044 | t0001 | g0180 | AFR | YRI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | CHB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | CHB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18906 | hp1 | a0001 | c0034 | t0002 | g0047 | AFR | YRI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18906 | hp2 | a0004 | c0014 | t0002 | g0059 | AFR | YRI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18939 | hp2 | a0015 | c0045 | t0001 | g0179 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18947 | hp2 | a0001 | c0004 | t0001 | g0017 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18950 | hp1 | a0016 | c0030 | t0001 | g0141 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18954 | hp1 | a0001 | c0028 | t0002 | g0096 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18954 | hp2 | a0001 | c0039 | t0001 | g0151 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18967 | hp1 | a0001 | c0001 | t0014 | g0228 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18984 | hp1 | a0017 | c0050 | t0001 | g0211 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18985 | hp1 | a0018 | c0040 | t0003 | g0178 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18998 | hp1 | a0001 | c0004 | t0001 | g0147 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19000 | hp2 | a0001 | c0004 | t0001 | g0191 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19030 | hp1 | a0001 | c0010 | t0001 | g0031 | AFR | LWK | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19055 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19068 | hp2 | a0001 | c0041 | t0006 | g0045 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19074 | hp2 | a0001 | c0004 | t0001 | g0148 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19091 | hp1 | a0019 | c0043 | t0001 | g0113 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19240 | hp1 | a0001 | c0009 | t0001 | g0218 | AFR | YRI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19240 | hp2 | a0001 | c0021 | t0004 | g0110 | AFR | YRI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ASW | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20129 | hp2 | a0001 | c0019 | t0002 | g0105 | AFR | ASW | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20752 | hp1 | a0001 | c0016 | t0013 | g0227 | EUR | TSI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0086 | EUR | TSI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | TSI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0085 | SAS | GIH | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0080 | SAS | GIH | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0097 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | USA | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG06807 | hp2 | a0004 | c0014 | t0002 | g0058 | AFR | USA | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20300 | hp1 | a0002 | c0007 | t0004 | g0028 | AFR | USA | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20300 | hp2 | a0001 | c0004 | t0001 | g0149 | AFR | USA | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0102 | AFR | LWK | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA21309 | hp2 | a0001 | c0005 | t0001 | g0214 | AFR | LWK | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0203 | REF | REF | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0066 | REF | REF | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:1472297 | G | A | 1 | a0011 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.6160C>T | p.Leu2054Phe | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/48 | 6268/6981 | 6160/6573 | 2054/2190 | chr7 | 1472297 | |||
chr7:1473172 | G | C | 1 | a0018 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.5970C>G | p.Phe1990Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/48 | 6078/6981 | 5970/6573 | 1990/2190 | chr7 | 1473172 | |||
chr7:1474299 | G | A | 1 | a0019 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.5698C>T | p.Arg1900Trp | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/48 | 5806/6981 | 5698/6573 | 1900/2190 | chr7 | 1474299 | |||
chr7:1474801 | G | A | 1 | a0010 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.5540C>T | p.Ala1847Val | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/48 | 5648/6981 | 5540/6573 | 1847/2190 | chr7 | 1474801 | |||
chr7:1475998 | G | A | 1 | a0002 | 3 | HG02723.hp1 HG03130.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.5452C>T | p.Pro1818Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/48 | 5560/6981 | 5452/6573 | 1818/2190 | chr7 | 1475998 | |||
chr7:1477771 | G | A | 1 | a0014 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.4796C>T | p.Pro1599Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 34/48 | 4904/6981 | 4796/6573 | 1599/2190 | chr7 | 1477771 | |||
chr7:1477864 | G | A | 1 | a0015 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.4703C>T | p.Ala1568Val | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 34/48 | 4811/6981 | 4703/6573 | 1568/2190 | chr7 | 1477864 | |||
chr7:1479480 | G | A | 1 | a0013 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.4279C>T | p.Arg1427Cys | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/48 | 4387/6981 | 4279/6573 | 1427/2190 | chr7 | 1479480 | |||
chr7:1479642 | G | C | 1 | a0009 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.4117C>G | p.Pro1373Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/48 | 4225/6981 | 4117/6573 | 1373/2190 | chr7 | 1479642 | |||
chr7:1480360 | C | T | 1 | a0003 | 2 | HG03041.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.4031G>A | p.Arg1344Gln | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/48 | 4139/6981 | 4031/6573 | 1344/2190 | chr7 | 1480360 | |||
chr7:1482686 | G | A | 1 | a0006 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.3563C>T | p.Ala1188Val | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/48 | 3671/6981 | 3563/6573 | 1188/2190 | chr7 | 1482686 | |||
chr7:1486639 | C | T | 1 | a0007 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.2962G>A | p.Val988Met | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/48 | 3070/6981 | 2962/6573 | 988/2190 | chr7 | 1486639 | |||
chr7:1497225 | CTGCTTGA others(38): Show |
C | 1 | a0008 | 1 | HG02056.hp2 | disruptive_inframe_deletion | MODERATE | c.1470_1514delCTACCT others(39): Show |
p.Asp490_Gln505delin others(4): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/48 | 1622/6981 | 1470/6573 | 490/2190 | chr7 | 1497225 | |||
chr7:1498981 | G | T | 1 | a0008 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.1131C>A | p.Asn377Lys | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/48 | 1239/6981 | 1131/6573 | 377/2190 | chr7 | 1498981 | |||
chr7:1499003 | T | C | 1 | a0004 | 2 | HG06807.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.1109A>G | p.Lys370Arg | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/48 | 1217/6981 | 1109/6573 | 370/2190 | chr7 | 1499003 | |||
chr7:1499626 | T | C | 1 | a0005 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.691A>G | p.Ile231Val | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 6/48 | 799/6981 | 691/6573 | 231/2190 | chr7 | 1499626 | |||
chr7:1500280 | C | G | 1 | a0016 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.436G>C | p.Val146Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 4/48 | 544/6981 | 436/6573 | 146/2190 | chr7 | 1500280 | |||
chr7:1503179 | G | C | 1 | a0017 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.71C>G | p.Pro24Arg | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/48 | 179/6981 | 71/6573 | 24/2190 | chr7 | 1503179 | |||
chr7:1503951 | C | T | 1 | a0012 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.10G>A | p.Ala4Thr | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/48 | 118/6981 | 10/6573 | 4/2190 | chr7 | 1503951 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:1471195 | G | A | 1 | a0001c0009 | 3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.6285C>T | p.Ala2095Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 46/48 | 6393/6981 | 6285/6573 | 2095/2190 | chr7 | 1471195 | |||
chr7:1471198 | C | T | 1 | a0001c0042 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.6282G>A | p.Ser2094Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 46/48 | 6390/6981 | 6282/6573 | 2094/2190 | chr7 | 1471198 | |||
chr7:1471637 | C | T | 3 | a0001c0018 a0001c0021 a0002c0007 |
5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
synonymous_variant | LOW | c.6189G>A | p.Leu2063Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 45/48 | 6297/6981 | 6189/6573 | 2063/2190 | chr7 | 1471637 | |||
chr7:1472307 | G | A | 1 | a0001c0009 | 3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.6150C>T | p.Tyr2050Tyr | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/48 | 6258/6981 | 6150/6573 | 2050/2190 | chr7 | 1472307 | |||
chr7:1473571 | C | T | 1 | a0001c0041 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.5952G>A | p.Pro1984Pro | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/48 | 6060/6981 | 5952/6573 | 1984/2190 | chr7 | 1473571 | |||
chr7:1473591 | G | A | 1 | a0001c0006 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
synonymous_variant | LOW | c.5932C>T | p.Leu1978Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/48 | 6040/6981 | 5932/6573 | 1978/2190 | chr7 | 1473591 | |||
chr7:1474170 | G | A | 1 | a0001c0008 | 3 | HG02738.hp1 HG03492.hp2 HG03831.hp1 |
splice_region_variant&synonymous_variant | LOW | c.5827C>T | p.Leu1943Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/48 | 5935/6981 | 5827/6573 | 1943/2190 | chr7 | 1474170 | |||
chr7:1474728 | C | T | 2 | a0001c0003 a0012c0017 |
9 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(6): Show |
synonymous_variant | LOW | c.5613G>A | p.Val1871Val | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/48 | 5721/6981 | 5613/6573 | 1871/2190 | chr7 | 1474728 | |||
chr7:1476825 | G | T | 1 | a0009c0033 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.5032C>A | p.Arg1678Arg | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 36/48 | 5140/6981 | 5032/6573 | 1678/2190 | chr7 | 1476825 | |||
chr7:1477607 | G | A | 1 | a0001c0008 | 3 | HG02738.hp1 HG03492.hp2 HG03831.hp1 |
synonymous_variant | LOW | c.4881C>T | p.Pro1627Pro | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/48 | 4989/6981 | 4881/6573 | 1627/2190 | chr7 | 1477607 | |||
chr7:1478499 | C | T | 2 | a0001c0019 a0001c0020 |
2 | HG01109.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.4497G>A | p.Gly1499Gly | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/48 | 4605/6981 | 4497/6573 | 1499/2190 | chr7 | 1478499 | |||
chr7:1478790 | C | A | 2 | a0001c0019 a0001c0020 |
2 | HG01109.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.4425G>T | p.Gly1475Gly | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 32/48 | 4533/6981 | 4425/6573 | 1475/2190 | chr7 | 1478790 | |||
chr7:1478865 | G | A | 1 | a0001c0009 | 3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.4350C>T | p.Thr1450Thr | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 32/48 | 4458/6981 | 4350/6573 | 1450/2190 | chr7 | 1478865 | |||
chr7:1480896 | G | A | 2 | a0001c0006 a0001c0036 |
5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
synonymous_variant | LOW | c.3888C>T | p.Arg1296Arg | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 29/48 | 3996/6981 | 3888/6573 | 1296/2190 | chr7 | 1480896 | |||
chr7:1482706 | G | A | 4 | a0001c0006 a0001c0009 a0001c0034 others(1): Show |
9 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
splice_region_variant&synonymous_variant | LOW | c.3543C>T | p.Ala1181Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/48 | 3651/6981 | 3543/6573 | 1181/2190 | chr7 | 1482706 | |||
chr7:1483815 | G | A | 1 | a0001c0035 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.3468C>T | p.Ser1156Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/48 | 3576/6981 | 3468/6573 | 1156/2190 | chr7 | 1483815 | |||
chr7:1484093 | C | A | 2 | a0001c0009 a0001c0047 |
4 | HG02647.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.3339G>T | p.Ser1113Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/48 | 3447/6981 | 3339/6573 | 1113/2190 | chr7 | 1484093 | |||
chr7:1484093 | C | T | 1 | a0001c0018 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.3339G>A | p.Ser1113Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/48 | 3447/6981 | 3339/6573 | 1113/2190 | chr7 | 1484093 | |||
chr7:1484099 | G | A | 5 | a0001c0008 a0001c0018 a0001c0021 others(2): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
synonymous_variant | LOW | c.3333C>T | p.Ala1111Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/48 | 3441/6981 | 3333/6573 | 1111/2190 | chr7 | 1484099 | |||
chr7:1484117 | C | T | 1 | a0003c0015 | 2 | HG03041.hp2 HG03139.hp2 |
synonymous_variant | LOW | c.3315G>A | p.Ser1105Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/48 | 3423/6981 | 3315/6573 | 1105/2190 | chr7 | 1484117 | |||
chr7:1485323 | G | A | 1 | a0001c0013 | 2 | HG01257.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.3123C>T | p.Ser1041Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 23/48 | 3231/6981 | 3123/6573 | 1041/2190 | chr7 | 1485323 | |||
chr7:1485334 | G | A | 1 | a0001c0036 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.3112C>T | p.Leu1038Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 23/48 | 3220/6981 | 3112/6573 | 1038/2190 | chr7 | 1485334 | |||
chr7:1485461 | C | T | 1 | a0018c0040 | 1 | NA18985.hp1 | synonymous_variant | LOW | c.2985G>A | p.Ser995Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 23/48 | 3093/6981 | 2985/6573 | 995/2190 | chr7 | 1485461 | |||
chr7:1486655 | G | A | 1 | a0001c0006 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
synonymous_variant | LOW | c.2946C>T | p.Ser982Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/48 | 3054/6981 | 2946/6573 | 982/2190 | chr7 | 1486655 | |||
chr7:1486664 | G | A | 1 | a0001c0016 | 2 | HG01074.hp1 NA20752.hp1 |
synonymous_variant | LOW | c.2937C>T | p.Leu979Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/48 | 3045/6981 | 2937/6573 | 979/2190 | chr7 | 1486664 | |||
chr7:1487024 | C | T | 1 | a0001c0019 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.2724G>A | p.Gln908Gln | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/48 | 2832/6981 | 2724/6573 | 908/2190 | chr7 | 1487024 | |||
chr7:1487939 | C | T | 1 | a0001c0023 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.2337G>A | p.Pro779Pro | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/48 | 2445/6981 | 2337/6573 | 779/2190 | chr7 | 1487939 | |||
chr7:1489670 | C | T | 1 | a0001c0018 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.2178G>A | p.Pro726Pro | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 17/48 | 2286/6981 | 2178/6573 | 726/2190 | chr7 | 1489670 | |||
chr7:1493084 | C | T | 1 | a0001c0039 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.2091G>A | p.Gly697Gly | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/48 | 2199/6981 | 2091/6573 | 697/2190 | chr7 | 1493084 | |||
chr7:1493877 | A | G | 40 | a0001c0001 a0001c0003 a0001c0004 others(37): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
synonymous_variant | LOW | c.1945T>C | p.Leu649Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/48 | 2053/6981 | 1945/6573 | 649/2190 | chr7 | 1493877 | |||
chr7:1496202 | C | T | 1 | a0001c0004 | 7 | HG00408.hp2 HG02129.hp1 NA18947.hp2 others(4): Show |
synonymous_variant | LOW | c.1665G>A | p.Ala555Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/48 | 1773/6981 | 1665/6573 | 555/2190 | chr7 | 1496202 | |||
chr7:1497267 | G | A | 2 | a0001c0019 a0001c0020 |
2 | HG01109.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.1473C>T | p.Tyr491Tyr | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/48 | 1581/6981 | 1473/6573 | 491/2190 | chr7 | 1497267 | |||
chr7:1498430 | G | A | 1 | a0001c0048 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.1407C>T | p.Ser469Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/48 | 1515/6981 | 1407/6573 | 469/2190 | chr7 | 1498430 | |||
chr7:1498481 | G | A | 1 | a0001c0006 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
synonymous_variant | LOW | c.1356C>T | p.Ser452Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/48 | 1464/6981 | 1356/6573 | 452/2190 | chr7 | 1498481 | |||
chr7:1498511 | G | A | 3 | a0001c0003 a0001c0037 a0012c0017 |
10 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(7): Show |
synonymous_variant | LOW | c.1326C>T | p.Ile442Ile | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/48 | 1434/6981 | 1326/6573 | 442/2190 | chr7 | 1498511 | |||
chr7:1498538 | C | T | 1 | a0001c0010 | 3 | HG02280.hp1 HG02451.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.1299G>A | p.Ala433Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/48 | 1407/6981 | 1299/6573 | 433/2190 | chr7 | 1498538 | |||
chr7:1498760 | G | A | 1 | a0001c0049 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.1230C>T | p.Ile410Ile | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/48 | 1338/6981 | 1230/6573 | 410/2190 | chr7 | 1498760 | |||
chr7:1498790 | G | A | 1 | a0001c0038 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1200C>T | p.Ser400Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/48 | 1308/6981 | 1200/6573 | 400/2190 | chr7 | 1498790 | |||
chr7:1498978 | G | A | 19 | a0001c0001 a0001c0004 a0001c0010 others(16): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
synonymous_variant | LOW | c.1134C>T | p.Pro378Pro | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/48 | 1242/6981 | 1134/6573 | 378/2190 | chr7 | 1498978 | |||
chr7:1499302 | G | A | 1 | a0001c0028 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.903C>T | p.Ile301Ile | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/48 | 1011/6981 | 903/6573 | 301/2190 | chr7 | 1499302 | |||
chr7:1499335 | C | T | 1 | a0001c0031 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.870G>A | p.Thr290Thr | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/48 | 978/6981 | 870/6573 | 290/2190 | chr7 | 1499335 | |||
chr7:1499582 | G | A | 1 | a0001c0011 | 3 | HG00639.hp1 HG01081.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.735C>T | p.His245His | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 6/48 | 843/6981 | 735/6573 | 245/2190 | chr7 | 1499582 | |||
chr7:1503061 | G | A | 32 | a0001c0001 a0001c0003 a0001c0004 others(29): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
synonymous_variant | LOW | c.189C>T | p.Ala63Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/48 | 297/6981 | 189/6573 | 63/2190 | chr7 | 1503061 | |||
chr7:1503178 | T | C | 31 | a0001c0001 a0001c0003 a0001c0004 others(28): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
synonymous_variant | LOW | c.72A>G | p.Pro24Pro | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/48 | 180/6981 | 72/6573 | 24/2190 | chr7 | 1503178 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:1470290 | G | A | 1 | a0001c0002t0008 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*287C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 287 | chr7 | 1470290 | ||||||
chr7:1470356 | CAGA | C | 2 | a0001c0006t0005 a0001c0036t0012 |
5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*218_*220delTCT | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 218 | chr7 | 1470356 | ||||||
chr7:1470376 | G | A | 1 | a0001c0006t0005 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*201C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 201 | chr7 | 1470376 | ||||||
chr7:1470465 | C | T | 1 | a0001c0001t0011 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 112 | chr7 | 1470465 | ||||||
chr7:1470479 | C | T | 1 | a0009c0033t0010 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*98G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 98 | chr7 | 1470479 | ||||||
chr7:1470536 | G | A | 3 | a0001c0001t0003 a0008c0032t0003 a0018c0040t0003 |
9 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*41C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 41 | chr7 | 1470536 | ||||||
chr7:1470541 | G | A | 1 | a0001c0002t0009 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*36C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 36 | chr7 | 1470541 | ||||||
chr7:1470546 | G | A | 6 | a0001c0008t0004 a0001c0008t0007 a0001c0018t0004 others(3): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*31C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 31 | chr7 | 1470546 | ||||||
chr7:1504345 | C | A | 36 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(33): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
5_prime_UTR_variant | MODIFIER | c.-64G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/48 | 385 | chr7 | 1504345 | ||||||
chr7:1504349 | G | A | 1 | a0001c0016t0013 | 1 | NA20752.hp1 | 5_prime_UTR_variant | MODIFIER | c.-68C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/48 | 389 | chr7 | 1504349 | ||||||
chr7:1504358 | A | AC | 3 | a0001c0001t0006 a0001c0008t0007 a0001c0041t0006 |
3 | HG03209.hp2 HG03831.hp1 NA19068.hp2 |
5_prime_UTR_variant | MODIFIER | c.-78dupG | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/48 | 399 | chr7 | 1504358 | ||||||
chr7:1504386 | T | A | 1 | a0001c0001t0014 | 1 | NA18967.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/48 | 426 | chr7 | 1504386 | ||||||
chr7:1504388 | T | A | 1 | a0001c0001t0014 | 1 | NA18967.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/48 | 428 | chr7 | 1504388 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:1470726 | G | A | 1 | a0001c0020t0002g0104 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6458-34C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 47/47 | chr7 | 1470726 | |||||||
chr7:1470760 | G | A | 2 | a0001c0008t0004g0019 a0001c0008t0007g0044 |
3 | HG02738.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.6458-68C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 47/47 | chr7 | 1470760 | |||||||
chr7:1470774 | C | T | 1 | a0001c0009t0001g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6457+72G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 47/47 | chr7 | 1470774 | |||||||
chr7:1470810 | G | A | 1 | a0001c0002t0002g0061 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.6457+36C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 47/47 | chr7 | 1470810 | |||||||
chr7:1471021 | G | T | 4 | a0001c0018t0004g0109 a0001c0021t0004g0110 a0002c0007t0004g0028 others(1): Show |
5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.6348-66C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 46/47 | chr7 | 1471021 | |||||||
chr7:1471024 | C | T | 2 | a0001c0009t0001g0042 a0001c0009t0001g0218 |
3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.6348-69G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 46/47 | chr7 | 1471024 | |||||||
chr7:1471325 | A | G | 1 | a0010c0026t0002g0068 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6256-101T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 45/47 | chr7 | 1471325 | |||||||
chr7:1471429 | G | A | 1 | a0014c0044t0001g0180 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6255+142C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 45/47 | chr7 | 1471429 | |||||||
chr7:1471446 | C | T | 1 | a0001c0002t0002g0024 | 2 | NA18982.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.6255+125G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 45/47 | chr7 | 1471446 | |||||||
chr7:1471648 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.6185-7G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471648 | |||||||
chr7:1471648 | CAGAG | C | 3 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 |
4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.6185-11_6185-8delC others(3): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471648 | |||||||
chr7:1471683 | G | T | 2 | a0001c0016t0001g0162 a0001c0016t0013g0227 |
2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.6185-42C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471683 | |||||||
chr7:1471795 | C | A | 1 | a0001c0002t0002g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6185-154G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471795 | |||||||
chr7:1471816 | C | T | 1 | a0001c0038t0001g0116 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6185-175G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471816 | |||||||
chr7:1471857 | C | T | 1 | a0001c0002t0002g0051 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6185-216G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471857 | |||||||
chr7:1471859 | C | T | 1 | a0001c0001t0003g0171 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.6185-218G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471859 | |||||||
chr7:1471868 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(148): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.6185-227T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471868 | |||||||
chr7:1471901 | G | A | 3 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 |
4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.6185-260C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471901 | |||||||
chr7:1471928 | C | T | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.6185-287G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471928 | |||||||
chr7:1471953 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.6185-312T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471953 | |||||||
chr7:1471962 | C | T | 1 | a0001c0002t0002g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.6184+311G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471962 | |||||||
chr7:1471984 | T | C | 26 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(23): Show |
32 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.6184+289A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471984 | |||||||
chr7:1472022 | C | T | 5 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 others(2): Show |
6 | HG01243.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.6184+251G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472022 | |||||||
chr7:1472162 | G | A | 2 | a0001c0004t0001g0148 a0001c0004t0001g0191 |
2 | NA19000.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.6184+111C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472162 | |||||||
chr7:1472183 | G | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG00621.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.6184+90C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472183 | |||||||
chr7:1472197 | G | A | 3 | a0001c0009t0001g0042 a0001c0009t0001g0218 a0001c0034t0002g0047 |
4 | HG02895.hp1 HG03130.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.6184+76C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472197 | |||||||
chr7:1472211 | G | T | 1 | a0001c0002t0002g0049 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.6184+62C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472211 | |||||||
chr7:1472248 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.6184+25C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472248 | |||||||
chr7:1472252 | G | A | 1 | a0001c0036t0012g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.6184+21C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472252 | |||||||
chr7:1472417 | C | G | 1 | a0001c0001t0001g0154 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.6071-31G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472417 | |||||||
chr7:1472418 | G | C | 1 | a0001c0001t0001g0154 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.6071-32C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472418 | |||||||
chr7:1472544 | C | T | 1 | a0001c0005t0001g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6071-158G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472544 | |||||||
chr7:1472569 | A | C | 1 | a0001c0005t0001g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6071-183T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472569 | |||||||
chr7:1472634 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.6071-248T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472634 | |||||||
chr7:1472666 | C | T | 6 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(3): Show |
9 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.6071-280G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472666 | |||||||
chr7:1472760 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6070+312C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472760 | |||||||
chr7:1472785 | G | A | 1 | a0001c0041t0006g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.6070+287C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472785 | |||||||
chr7:1472794 | C | CTGGTGGA | 17 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(14): Show |
19 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.6070+271_6070+277d others(9): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472794 | |||||||
chr7:1472847 | G | T | 7 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(4): Show |
10 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.6070+225C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472847 | |||||||
chr7:1472851 | G | A | 7 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(4): Show |
10 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.6070+221C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472851 | |||||||
chr7:1472855 | C | T | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6070+217G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472855 | |||||||
chr7:1472905 | G | T | 17 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0133 others(14): Show |
21 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.6070+167C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472905 | |||||||
chr7:1472966 | C | CATCGGGA others(11): Show |
1 | a0001c0001t0001g0154 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.6070+88_6070+105du others(19): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472966 | |||||||
chr7:1473002 | C | CA | 21 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(18): Show |
27 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.6070+69_6070+70ins others(1): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1473002 | |||||||
chr7:1473187 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0137 a0001c0001t0001g0193 |
4 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.5958-3C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473187 | |||||||
chr7:1473324 | C | T | 6 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0021t0004g0110 others(3): Show |
8 | HG02723.hp1 HG02738.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.5958-140G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473324 | |||||||
chr7:1473342 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0150 a0001c0001t0001g0204 |
4 | HG02723.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.5958-158C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473342 | |||||||
chr7:1473394 | G | A | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5957+172C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473394 | |||||||
chr7:1473454 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0206 |
2 | HG03704.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.5957+112C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473454 | |||||||
chr7:1473479 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0223 |
2 | HG00733.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.5957+87G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473479 | |||||||
chr7:1473480 | G | A | 1 | a0001c0001t0001g0016 | 3 | HG00438.hp1 HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.5957+86C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473480 | |||||||
chr7:1473709 | G | A | 1 | a0001c0035t0001g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.5830-16C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/47 | chr7 | 1473709 | |||||||
chr7:1473733 | G | A | 4 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 others(1): Show |
5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.5830-40C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/47 | chr7 | 1473733 | |||||||
chr7:1473775 | C | T | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5830-82G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/47 | chr7 | 1473775 | |||||||
chr7:1473980 | C | T | 2 | a0001c0005t0001g0212 a0001c0005t0001g0214 |
2 | HG01884.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.5829+188G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/47 | chr7 | 1473980 | |||||||
chr7:1474143 | G | C | 4 | a0001c0005t0001g0213 a0001c0019t0002g0105 a0001c0020t0002g0104 others(1): Show |
4 | HG01109.hp2 HG02258.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.5829+25C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/47 | chr7 | 1474143 | |||||||
chr7:1474391 | C | T | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5637-31G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474391 | |||||||
chr7:1474413 | C | G | 6 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(3): Show |
6 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.5637-53G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474413 | |||||||
chr7:1474420 | C | T | 1 | a0001c0020t0002g0104 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5637-60G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474420 | |||||||
chr7:1474471 | A | AAC | 156 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.5637-113_5637-112d others(4): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474471 | |||||||
chr7:1474531 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5637-171G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474531 | |||||||
chr7:1474573 | T | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.5636+132A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474573 | |||||||
chr7:1474660 | T | G | 3 | a0001c0002t0002g0009 a0001c0002t0002g0061 a0001c0002t0002g0074 |
6 | HG00423.hp1 HG00558.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.5636+45A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474660 | |||||||
chr7:1474952 | G | C | 1 | a0001c0001t0003g0171 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.5503-114C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1474952 | |||||||
chr7:1475013 | C | T | 1 | a0001c0036t0012g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5503-175G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475013 | |||||||
chr7:1475073 | G | T | 1 | a0001c0002t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5503-235C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475073 | |||||||
chr7:1475345 | G | A | 1 | a0001c0002t0002g0053 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.5503-507C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475345 | |||||||
chr7:1475398 | C | A | 1 | a0001c0002t0002g0083 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.5502+550G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475398 | |||||||
chr7:1475433 | C | T | 1 | a0001c0002t0002g0022 | 2 | HG03017.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.5502+515G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475433 | |||||||
chr7:1475497 | A | C | 2 | a0001c0002t0002g0021 a0005c0029t0002g0098 |
3 | HG00642.hp2 HG01123.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.5502+451T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475497 | |||||||
chr7:1475539 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0019c0043t0001g0113 |
3 | NA19009.hp1 NA19081.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.5502+409C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475539 | |||||||
chr7:1475589 | C | T | 1 | a0001c0002t0002g0103 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.5502+359G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475589 | |||||||
chr7:1475595 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0205 |
3 | HG02559.hp1 HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.5502+353G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475595 | |||||||
chr7:1475615 | C | T | 1 | a0001c0002t0002g0015 | 3 | HG01069.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.5502+333G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475615 | |||||||
chr7:1475778 | G | A | 4 | a0001c0018t0004g0109 a0001c0021t0004g0110 a0002c0007t0004g0028 others(1): Show |
5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.5502+170C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475778 | |||||||
chr7:1475824 | C | T | 1 | a0001c0002t0002g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5502+124G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475824 | |||||||
chr7:1475898 | G | A | 1 | a0001c0002t0002g0026 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.5502+50C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475898 | |||||||
chr7:1475928 | C | T | 8 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0056 others(5): Show |
16 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.5502+20G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475928 | |||||||
chr7:1475929 | G | A | 3 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 |
4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.5502+19C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475929 | |||||||
chr7:1476078 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02615.hp1 | splice_region_variant&intron_variant | LOW | c.5379-7C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 38/47 | chr7 | 1476078 | |||||||
chr7:1476084 | G | C | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.5379-13C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 38/47 | chr7 | 1476084 | |||||||
chr7:1476134 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5379-63C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 38/47 | chr7 | 1476134 | |||||||
chr7:1476482 | G | A | 1 | a0001c0036t0012g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5152-27C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 37/47 | chr7 | 1476482 | |||||||
chr7:1476493 | G | GCCTCTCC others(14): Show |
105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(102): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.5151+56_5152-39dup others(21): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 37/47 | chr7 | 1476493 | |||||||
chr7:1476493 | G | GCCTCTCC others(35): Show |
1 | a0001c0001t0001g0222 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5151+35_5152-39dup others(42): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 37/47 | chr7 | 1476493 | |||||||
chr7:1476538 | T | C | 1 | a0001c0036t0012g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5151+32A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 37/47 | chr7 | 1476538 | |||||||
chr7:1476553 | A | G | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5151+17T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 37/47 | chr7 | 1476553 | |||||||
chr7:1476671 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.5064-14T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 36/47 | chr7 | 1476671 | |||||||
chr7:1476725 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.5064-68G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 36/47 | chr7 | 1476725 | |||||||
chr7:1476727 | G | C | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5063+67C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 36/47 | chr7 | 1476727 | |||||||
chr7:1477066 | G | A | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4939-148C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477066 | |||||||
chr7:1477139 | G | A | 5 | a0001c0002t0002g0049 a0001c0018t0004g0109 a0001c0021t0004g0110 others(2): Show |
6 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.4939-221C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477139 | |||||||
chr7:1477227 | C | A | 1 | a0001c0001t0001g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4939-309G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477227 | |||||||
chr7:1477352 | G | A | 1 | a0001c0005t0001g0117 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.4938+198C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477352 | |||||||
chr7:1477401 | T | A | 1 | a0001c0002t0002g0082 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.4938+149A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477401 | |||||||
chr7:1477425 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4938+125C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477425 | |||||||
chr7:1477465 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4938+85C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477465 | |||||||
chr7:1477470 | G | A | 1 | a0001c0019t0002g0105 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4938+80C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477470 | |||||||
chr7:1477526 | G | A | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4938+24C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477526 | |||||||
chr7:1477700 | G | C | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02630.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4815-27C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 34/47 | chr7 | 1477700 | |||||||
chr7:1477945 | G | A | 1 | a0001c0002t0002g0052 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4631-9C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1477945 | |||||||
chr7:1478030 | G | T | 6 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(3): Show |
8 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.4631-94C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478030 | |||||||
chr7:1478033 | T | A | 1 | a0001c0012t0001g0118 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4631-97A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478033 | |||||||
chr7:1478064 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.4631-128T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478064 | |||||||
chr7:1478076 | G | T | 4 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(1): Show |
4 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.4631-140C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478076 | |||||||
chr7:1478082 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.4631-146T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478082 | |||||||
chr7:1478096 | AGGAGAGT others(12): Show |
A | 2 | a0001c0001t0001g0037 a0001c0003t0001g0197 |
3 | HG01070.hp1 HG01243.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.4631-179_4631-161d others(21): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478096 | |||||||
chr7:1478105 | C | T | 1 | a0001c0005t0001g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4631-169G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478105 | |||||||
chr7:1478115 | T | C | 2 | a0001c0005t0001g0138 a0001c0005t0001g0139 |
2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.4631-179A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478115 | |||||||
chr7:1478161 | T | C | 2 | a0001c0009t0001g0042 a0001c0009t0001g0218 |
3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4630+205A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478161 | |||||||
chr7:1478230 | G | A | 9 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(6): Show |
11 | HG01109.hp2 HG02280.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.4630+136C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478230 | |||||||
chr7:1478335 | G | A | 9 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0025 others(6): Show |
18 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.4630+31C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478335 | |||||||
chr7:1478555 | C | T | 2 | a0001c0005t0001g0138 a0001c0005t0001g0139 |
2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.4490-49G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 32/47 | chr7 | 1478555 | |||||||
chr7:1478700 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.4489+26C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 32/47 | chr7 | 1478700 | |||||||
chr7:1478909 | G | T | 1 | a0001c0002t0002g0015 | 3 | HG01069.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.4330-24C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1478909 | |||||||
chr7:1478930 | C | T | 4 | a0001c0003t0001g0030 a0001c0003t0001g0195 a0001c0037t0001g0196 others(1): Show |
5 | HG02257.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.4330-45G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1478930 | |||||||
chr7:1479054 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4330-169C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1479054 | |||||||
chr7:1479112 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4330-227G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1479112 | |||||||
chr7:1479233 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.4329+197A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1479233 | |||||||
chr7:1479247 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4329+183C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1479247 | |||||||
chr7:1479375 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.4329+55C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1479375 | |||||||
chr7:1479725 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.4075-41T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1479725 | |||||||
chr7:1479756 | G | A | 1 | a0001c0001t0003g0170 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4075-72C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1479756 | |||||||
chr7:1479909 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0159 |
2 | NA18950.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.4075-225C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1479909 | |||||||
chr7:1479938 | G | A | 1 | a0010c0026t0002g0068 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4075-254C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1479938 | |||||||
chr7:1480100 | A | G | 1 | a0001c0006t0005g0043 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.4074+217T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1480100 | |||||||
chr7:1480128 | T | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0114 |
2 | NA19009.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.4074+189A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1480128 | |||||||
chr7:1480191 | C | T | 6 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.4074+126G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1480191 | |||||||
chr7:1480256 | C | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.4074+61G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1480256 | |||||||
chr7:1480268 | G | A | 4 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 others(1): Show |
5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.4074+49C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1480268 | |||||||
chr7:1480310 | A | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
splice_region_variant&intron_variant | LOW | c.4074+7T>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1480310 | |||||||
chr7:1480527 | G | A | 14 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(11): Show |
19 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.3950-86C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 29/47 | chr7 | 1480527 | |||||||
chr7:1480531 | G | A | 1 | a0001c0008t0007g0044 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3950-90C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 29/47 | chr7 | 1480531 | |||||||
chr7:1480636 | G | A | 4 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 others(1): Show |
5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3950-195C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 29/47 | chr7 | 1480636 | |||||||
chr7:1480643 | C | A | 6 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3949+192G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 29/47 | chr7 | 1480643 | |||||||
chr7:1480707 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3949+128C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 29/47 | chr7 | 1480707 | |||||||
chr7:1480965 | C | T | 5 | a0001c0018t0004g0109 a0001c0021t0004g0110 a0001c0022t0004g0111 others(2): Show |
6 | HG02280.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.3851-32G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 28/47 | chr7 | 1480965 | |||||||
chr7:1481207 | G | A | 13 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(10): Show |
15 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.3850+135C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 28/47 | chr7 | 1481207 | |||||||
chr7:1481315 | C | G | 6 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3850+27G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 28/47 | chr7 | 1481315 | |||||||
chr7:1481321 | C | T | 1 | a0001c0008t0004g0019 | 2 | HG02738.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3850+21G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 28/47 | chr7 | 1481321 | |||||||
chr7:1481554 | G | A | 1 | a0001c0005t0001g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3704-66C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481554 | |||||||
chr7:1481577 | A | G | 1 | a0001c0035t0001g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3704-89T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481577 | |||||||
chr7:1481608 | C | T | 1 | a0001c0036t0012g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3704-120G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481608 | |||||||
chr7:1481616 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3704-128G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481616 | |||||||
chr7:1481630 | AAGACCTG others(101): Show |
A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0157 others(4): Show |
14 | HG00438.hp1 HG01099.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.3704-250_3704-143d others(2): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481630 | |||||||
chr7:1481653 | G | A | 3 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 |
4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3704-165C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481653 | |||||||
chr7:1481670 | C | A | 15 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(12): Show |
20 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.3704-182G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481670 | |||||||
chr7:1481695 | C | A | 3 | a0001c0001t0003g0012 a0001c0001t0003g0163 a0001c0001t0003g0171 |
4 | HG00558.hp2 HG00597.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.3704-207G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481695 | |||||||
chr7:1481903 | G | A | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3704-415C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481903 | |||||||
chr7:1481947 | C | A | 1 | a0001c0002t0002g0077 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3704-459G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481947 | |||||||
chr7:1481967 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0216 |
3 | HG02109.hp1 HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3704-479G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481967 | |||||||
chr7:1482086 | C | T | 6 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3703+460G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482086 | |||||||
chr7:1482239 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.3703+307A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482239 | |||||||
chr7:1482311 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0184 |
4 | HG01891.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3703+235C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482311 | |||||||
chr7:1482319 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3703+227G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482319 | |||||||
chr7:1482337 | C | T | 2 | a0001c0002t0002g0069 a0001c0002t0002g0094 |
2 | HG02083.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.3703+209G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482337 | |||||||
chr7:1482497 | C | T | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3703+49G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482497 | |||||||
chr7:1482498 | G | A | 8 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(5): Show |
11 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3703+48C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482498 | |||||||
chr7:1482521 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.3703+25A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482521 | |||||||
chr7:1482539 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
splice_region_variant&intron_variant | LOW | c.3703+7T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482539 | |||||||
chr7:1482777 | A | T | 16 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(13): Show |
21 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.3542-70T>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1482777 | |||||||
chr7:1482920 | A | G | 3 | a0001c0002t0002g0007 a0001c0002t0002g0093 a0001c0002t0008g0067 |
6 | HG00544.hp2 HG01943.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.3542-213T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1482920 | |||||||
chr7:1482971 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.3542-264T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1482971 | |||||||
chr7:1483017 | T | A | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.3542-310A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483017 | |||||||
chr7:1483129 | T | C | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3542-422A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483129 | |||||||
chr7:1483213 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.3542-506C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483213 | |||||||
chr7:1483248 | G | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.3541+494C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483248 | |||||||
chr7:1483282 | C | G | 16 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(13): Show |
21 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.3541+460G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483282 | |||||||
chr7:1483283 | G | A | 1 | a0001c0002t0002g0088 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3541+459C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483283 | |||||||
chr7:1483326 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3541+416C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483326 | |||||||
chr7:1483352 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.3541+390G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483352 | |||||||
chr7:1483456 | G | A | 8 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(5): Show |
11 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3541+286C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483456 | |||||||
chr7:1483587 | G | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0127 a0001c0001t0001g0128 |
4 | HG00140.hp1 HG00280.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.3541+155C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483587 | |||||||
chr7:1483602 | G | T | 1 | a0001c0013t0002g0023 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3541+140C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483602 | |||||||
chr7:1483604 | G | C | 1 | a0001c0038t0001g0116 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3541+138C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483604 | |||||||
chr7:1483626 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3541+116C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483626 | |||||||
chr7:1483631 | G | C | 2 | a0001c0001t0001g0129 a0001c0041t0006g0045 |
2 | NA19068.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.3541+111C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483631 | |||||||
chr7:1483859 | G | A | 5 | a0001c0018t0004g0109 a0001c0021t0004g0110 a0001c0022t0004g0111 others(2): Show |
6 | HG02280.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.3430-6C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/47 | chr7 | 1483859 | |||||||
chr7:1483883 | A | G | 9 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(6): Show |
12 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3430-30T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/47 | chr7 | 1483883 | |||||||
chr7:1483923 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.3430-70A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/47 | chr7 | 1483923 | |||||||
chr7:1484192 | G | A | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3262-22C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484192 | |||||||
chr7:1484320 | A | C | 1 | a0001c0005t0001g0117 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3262-150T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484320 | |||||||
chr7:1484320 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.3262-150T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484320 | |||||||
chr7:1484384 | A | G | 8 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0056 others(5): Show |
16 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.3262-214T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484384 | |||||||
chr7:1484448 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0169 |
2 | HG00099.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3262-278A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484448 | |||||||
chr7:1484481 | C | G | 1 | a0001c0002t0002g0075 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3262-311G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484481 | |||||||
chr7:1484593 | CAT | C | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.3262-425_3262-424d others(4): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484593 | |||||||
chr7:1484602 | T | C | 1 | a0001c0036t0012g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3262-432A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484602 | |||||||
chr7:1484635 | C | T | 13 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(10): Show |
18 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.3261+463G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484635 | |||||||
chr7:1484636 | G | A | 1 | a0001c0002t0002g0053 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3261+462C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484636 | |||||||
chr7:1484659 | C | T | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.3261+439G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484659 | |||||||
chr7:1484665 | G | A | 5 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(2): Show |
5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3261+433C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484665 | |||||||
chr7:1484667 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3261+431C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484667 | |||||||
chr7:1484717 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0019c0043t0001g0113 |
3 | NA19009.hp1 NA19081.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3261+381G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484717 | |||||||
chr7:1484723 | C | A | 3 | a0001c0009t0001g0042 a0001c0009t0001g0218 a0001c0034t0002g0047 |
4 | HG02895.hp1 HG03130.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3261+375G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484723 | |||||||
chr7:1484821 | C | T | 1 | a0001c0002t0002g0093 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3261+277G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484821 | |||||||
chr7:1484847 | C | T | 5 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(2): Show |
5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3261+251G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484847 | |||||||
chr7:1484866 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3261+232A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484866 | |||||||
chr7:1484943 | A | ACCCCGTC others(64): Show |
1 | a0001c0001t0001g0159 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3261+154_3261+155i others(73): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | |||||||
chr7:1484943 | A | ACCCCGTC others(28): Show |
14 | a0001c0001t0001g0034 a0001c0001t0001g0192 a0001c0001t0001g0223 others(11): Show |
18 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.3261+120_3261+154d others(37): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | |||||||
chr7:1484943 | A | ACCCCGTC others(63): Show |
116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.3261+85_3261+154du others(71): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | |||||||
chr7:1484943 | A | ACCCCGTC others(98): Show |
3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02630.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3261+50_3261+154du others(106): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | |||||||
chr7:1484943 | A | ACCCCGTC others(64): Show |
1 | a0001c0001t0001g0160 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3261+154_3261+155i others(73): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | |||||||
chr7:1484943 | ACCCCGTC others(28): Show |
A | 3 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 |
4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3261+120_3261+154d others(37): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | |||||||
chr7:1484943 | ACCCCGTC others(63): Show |
A | 7 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(4): Show |
8 | HG01884.hp1 HG02738.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.3261+85_3261+154de others(71): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | |||||||
chr7:1485077 | T | C | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3261+21A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1485077 | |||||||
chr7:1485226 | G | A | 6 | a0001c0002t0002g0004 a0001c0002t0002g0056 a0001c0002t0002g0062 others(3): Show |
11 | HG00140.hp2 HG00639.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.3157-24C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 23/47 | chr7 | 1485226 | |||||||
chr7:1485504 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2977-35C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485504 | |||||||
chr7:1485566 | G | A | 11 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(8): Show |
16 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.2977-97C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485566 | |||||||
chr7:1485606 | G | A | 1 | a0001c0002t0002g0074 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2977-137C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485606 | |||||||
chr7:1485627 | T | C | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2977-158A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485627 | |||||||
chr7:1485686 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2977-217A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485686 | |||||||
chr7:1485789 | G | A | 13 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0205 others(10): Show |
17 | HG02109.hp1 HG02280.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.2977-320C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485789 | |||||||
chr7:1485886 | C | G | 2 | a0001c0002t0002g0075 a0001c0002t0002g0076 |
2 | NA18747.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.2977-417G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485886 | |||||||
chr7:1485927 | T | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2977-458A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485927 | |||||||
chr7:1486125 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2976+500T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486125 | |||||||
chr7:1486133 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.2976+492G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486133 | |||||||
chr7:1486172 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2976+453C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486172 | |||||||
chr7:1486196 | A | G | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2976+429T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486196 | |||||||
chr7:1486269 | AT | A | 18 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0167 others(15): Show |
20 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.2976+355delA | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486269 | |||||||
chr7:1486273 | T | A | 15 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(12): Show |
20 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.2976+352A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486273 | |||||||
chr7:1486274 | T | A | 13 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(10): Show |
15 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.2976+351A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486274 | |||||||
chr7:1486333 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2976+292C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486333 | |||||||
chr7:1486434 | T | C | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2976+191A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486434 | |||||||
chr7:1486447 | T | C | 1 | a0004c0014t0002g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2976+178A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486447 | |||||||
chr7:1486545 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.2976+80C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486545 | |||||||
chr7:1486591 | G | A | 1 | a0001c0002t0002g0048 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2976+34C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486591 | |||||||
chr7:1486599 | G | A | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2976+26C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486599 | |||||||
chr7:1486820 | C | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(59): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.2827-46G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/47 | chr7 | 1486820 | |||||||
chr7:1486821 | G | A | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2827-47C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/47 | chr7 | 1486821 | |||||||
chr7:1486838 | C | T | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2827-64G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/47 | chr7 | 1486838 | |||||||
chr7:1486883 | G | A | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2826+39C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/47 | chr7 | 1486883 | |||||||
chr7:1486897 | G | A | 1 | a0001c0002t0002g0054 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2826+25C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/47 | chr7 | 1486897 | |||||||
chr7:1486898 | G | T | 11 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(8): Show |
15 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2826+24C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/47 | chr7 | 1486898 | |||||||
chr7:1487155 | G | A | 4 | a0001c0002t0002g0014 a0001c0002t0002g0024 a0001c0002t0002g0075 others(1): Show |
7 | HG00438.hp2 NA18747.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.2647-54C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487155 | |||||||
chr7:1487169 | T | C | 1 | a0001c0005t0001g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2647-68A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487169 | |||||||
chr7:1487175 | C | T | 5 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(2): Show |
5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2647-74G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487175 | |||||||
chr7:1487191 | G | A | 14 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(11): Show |
16 | HG01109.hp2 HG01884.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2647-90C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487191 | |||||||
chr7:1487210 | A | G | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2647-109T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487210 | |||||||
chr7:1487267 | G | T | 6 | a0001c0005t0001g0138 a0001c0005t0001g0139 a0001c0006t0005g0043 others(3): Show |
7 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.2646+53C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487267 | |||||||
chr7:1487310 | C | T | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2646+10G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487310 | |||||||
chr7:1487457 | C | T | 16 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(13): Show |
18 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.2517-8G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487457 | |||||||
chr7:1487486 | C | A | 6 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0021t0004g0110 others(3): Show |
8 | HG02723.hp1 HG02738.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.2517-37G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487486 | |||||||
chr7:1487509 | CCT | C | 3 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 |
4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2517-62_2517-61del others(2): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487509 | |||||||
chr7:1487534 | G | A | 1 | a0001c0041t0006g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2517-85C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487534 | |||||||
chr7:1487619 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.2516+141G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487619 | |||||||
chr7:1487690 | T | A | 1 | a0001c0031t0001g0124 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2516+70A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487690 | |||||||
chr7:1487693 | C | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0121 a0001c0001t0001g0166 others(1): Show |
7 | HG00544.hp1 HG00621.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.2516+67G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487693 | |||||||
chr7:1487694 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2516+66G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487694 | |||||||
chr7:1487738 | C | T | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2516+22G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487738 | |||||||
chr7:1487748 | T | C | 16 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(13): Show |
19 | HG01109.hp2 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.2516+12A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487748 | |||||||
chr7:1487969 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2319-12G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1487969 | |||||||
chr7:1488051 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2319-94G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488051 | |||||||
chr7:1488075 | A | G | 13 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(10): Show |
15 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.2319-118T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488075 | |||||||
chr7:1488099 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2319-142C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488099 | |||||||
chr7:1488157 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2319-200C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488157 | |||||||
chr7:1488159 | G | A | 1 | a0001c0019t0002g0105 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2319-202C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488159 | |||||||
chr7:1488193 | C | T | 2 | a0001c0002t0002g0097 a0011c0025t0002g0089 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2319-236G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488193 | |||||||
chr7:1488408 | G | A | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2319-451C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488408 | |||||||
chr7:1488506 | C | T | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2319-549G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488506 | |||||||
chr7:1488611 | G | A | 1 | a0001c0002t0002g0013 | 3 | HG01167.hp2 HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2319-654C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488611 | |||||||
chr7:1488671 | G | A | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2318+673C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488671 | |||||||
chr7:1488697 | G | T | 1 | a0001c0011t0001g0208 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2318+647C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488697 | |||||||
chr7:1488772 | G | A | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2318+572C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488772 | |||||||
chr7:1488778 | C | T | 5 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(2): Show |
5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2318+566G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488778 | |||||||
chr7:1488816 | C | A | 1 | a0001c0036t0012g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2318+528G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488816 | |||||||
chr7:1488937 | C | T | 1 | a0001c0038t0001g0116 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2318+407G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488937 | |||||||
chr7:1489025 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2318+319T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489025 | |||||||
chr7:1489048 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2318+296T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489048 | |||||||
chr7:1489087 | G | A | 1 | a0001c0002t0002g0025 | 2 | HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2318+257C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489087 | |||||||
chr7:1489104 | G | A | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2318+240C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489104 | |||||||
chr7:1489216 | G | A | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2318+128C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489216 | |||||||
chr7:1489236 | G | A | 1 | a0001c0002t0002g0054 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2318+108C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489236 | |||||||
chr7:1489244 | T | C | 3 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 |
4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2318+100A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489244 | |||||||
chr7:1489304 | C | T | 1 | a0001c0005t0001g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2318+40G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489304 | |||||||
chr7:1489308 | C | T | 1 | a0001c0008t0007g0044 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2318+36G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489308 | |||||||
chr7:1489311 | T | TCCCGGGC others(44): Show |
222 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2318+32_2318+33ins others(51): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489311 | |||||||
chr7:1489311 | T | TCCCGGGC others(44): Show |
1 | a0001c0001t0001g0174 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2318+32_2318+33ins others(51): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489311 | |||||||
chr7:1489311 | T | TCCCGGGC others(44): Show |
2 | a0001c0001t0001g0035 a0001c0001t0001g0216 |
3 | HG02109.hp1 HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2318+32_2318+33ins others(51): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489311 | |||||||
chr7:1489324 | G | GAGGGGAC others(44): Show |
1 | a0001c0002t0002g0078 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2318+19_2318+20ins others(51): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489324 | |||||||
chr7:1489466 | G | A | 1 | a0001c0038t0001g0116 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2258-62C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 17/47 | chr7 | 1489466 | |||||||
chr7:1489489 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0121 a0001c0001t0001g0166 others(1): Show |
7 | HG00544.hp1 HG00621.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258-85A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 17/47 | chr7 | 1489489 | |||||||
chr7:1489565 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.2257+26C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 17/47 | chr7 | 1489565 | |||||||
chr7:1489703 | G | A | 1 | a0001c0031t0001g0124 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2166-21C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489703 | |||||||
chr7:1489788 | G | A | 1 | a0001c0038t0001g0116 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2166-106C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489788 | |||||||
chr7:1489791 | C | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2166-109G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489791 | |||||||
chr7:1489796 | C | T | 7 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(4): Show |
10 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2166-114G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489796 | |||||||
chr7:1489825 | A | G | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2166-143T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489825 | |||||||
chr7:1489863 | G | A | 1 | a0001c0020t0002g0104 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2166-181C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489863 | |||||||
chr7:1489925 | G | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0002t0002g0079 |
3 | HG00621.hp1 HG02027.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.2166-243C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489925 | |||||||
chr7:1489935 | A | C | 4 | a0001c0002t0002g0027 a0001c0002t0002g0090 a0001c0002t0002g0097 others(1): Show |
5 | HG01891.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2166-253T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489935 | |||||||
chr7:1489950 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2166-268T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489950 | |||||||
chr7:1490002 | G | A | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2166-320C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490002 | |||||||
chr7:1490020 | T | C | 1 | a0014c0044t0001g0180 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2166-338A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490020 | |||||||
chr7:1490054 | C | T | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2166-372G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490054 | |||||||
chr7:1490089 | CAG | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2166-409_2166-408d others(4): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490089 | |||||||
chr7:1490125 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2166-443T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490125 | |||||||
chr7:1490224 | C | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2166-542G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490224 | |||||||
chr7:1490256 | G | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG00621.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.2166-574C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490256 | |||||||
chr7:1490420 | AC | A | 4 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 others(1): Show |
5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2166-739delG | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490420 | |||||||
chr7:1490434 | G | A | 6 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2166-752C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490434 | |||||||
chr7:1490451 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2166-769C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490451 | |||||||
chr7:1490486 | G | A | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2166-804C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490486 | |||||||
chr7:1490521 | G | A | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2166-839C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490521 | |||||||
chr7:1490561 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2166-879G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490561 | |||||||
chr7:1490746 | G | C | 1 | a0001c0004t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2166-1064C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490746 | |||||||
chr7:1490800 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2166-1118A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490800 | |||||||
chr7:1490829 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2166-1147A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490829 | |||||||
chr7:1490853 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2166-1171T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490853 | |||||||
chr7:1490858 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2166-1176T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490858 | |||||||
chr7:1490870 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2166-1188C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490870 | |||||||
chr7:1491148 | C | T | 1 | a0002c0007t0004g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2166-1466G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491148 | |||||||
chr7:1491153 | G | C | 1 | a0001c0002t0002g0083 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2166-1471C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491153 | |||||||
chr7:1491154 | C | T | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2166-1472G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491154 | |||||||
chr7:1491158 | G | A | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2166-1476C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491158 | |||||||
chr7:1491315 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02630.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2166-1633G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491315 | |||||||
chr7:1491316 | G | A | 2 | a0001c0048t0001g0189 a0014c0044t0001g0180 |
2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2166-1634C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491316 | |||||||
chr7:1491398 | G | C | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2165+1612C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491398 | |||||||
chr7:1491516 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2165+1494T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491516 | |||||||
chr7:1491624 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2165+1386C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491624 | |||||||
chr7:1491625 | G | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.2165+1385C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491625 | |||||||
chr7:1491769 | G | A | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2165+1241C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491769 | |||||||
chr7:1491803 | C | T | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2165+1207G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491803 | |||||||
chr7:1492047 | C | T | 8 | a0001c0002t0002g0002 a0001c0002t0002g0015 a0001c0002t0002g0050 others(5): Show |
15 | HG01069.hp1 HG01071.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.2165+963G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492047 | |||||||
chr7:1492148 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2165+862C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492148 | |||||||
chr7:1492179 | C | T | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2165+831G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492179 | |||||||
chr7:1492407 | G | A | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2165+603C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492407 | |||||||
chr7:1492521 | T | C | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2165+489A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492521 | |||||||
chr7:1492581 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.2165+429C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492581 | |||||||
chr7:1492613 | G | C | 1 | a0001c0036t0012g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2165+397C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492613 | |||||||
chr7:1492615 | G | C | 1 | a0001c0019t0002g0105 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2165+395C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492615 | |||||||
chr7:1492624 | C | CATT | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2165+385_2165+386i others(5): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492624 | |||||||
chr7:1492711 | C | G | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2165+299G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492711 | |||||||
chr7:1492734 | G | A | 9 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(6): Show |
12 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2165+276C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492734 | |||||||
chr7:1492748 | C | T | 15 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(12): Show |
19 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.2165+262G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492748 | |||||||
chr7:1492765 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2165+245C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492765 | |||||||
chr7:1492769 | T | C | 1 | a0001c0002t0002g0090 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2165+241A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492769 | |||||||
chr7:1492798 | T | C | 1 | a0001c0002t0002g0080 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2165+212A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492798 | |||||||
chr7:1492834 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2165+176G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492834 | |||||||
chr7:1492863 | C | T | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2165+147G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492863 | |||||||
chr7:1492866 | GGGCTTAC others(27): Show |
G | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2165+110_2165+143d others(36): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492866 | |||||||
chr7:1492899 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.2165+111G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492899 | |||||||
chr7:1492900 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2165+110T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492900 | |||||||
chr7:1492910 | G | A | 5 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(2): Show |
5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2165+100C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492910 | |||||||
chr7:1492925 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2165+85C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492925 | |||||||
chr7:1492943 | C | T | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2165+67G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492943 | |||||||
chr7:1492944 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2165+66C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492944 | |||||||
chr7:1492977 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2165+33G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492977 | |||||||
chr7:1492995 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2165+15C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492995 | |||||||
chr7:1493217 | G | A | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2069-111C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493217 | |||||||
chr7:1493273 | G | A | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2069-167C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493273 | |||||||
chr7:1493312 | G | A | 5 | a0001c0005t0001g0138 a0001c0005t0001g0139 a0001c0006t0005g0043 others(2): Show |
6 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.2069-206C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493312 | |||||||
chr7:1493372 | G | A | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2069-266C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493372 | |||||||
chr7:1493398 | G | A | 9 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(6): Show |
12 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2069-292C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493398 | |||||||
chr7:1493409 | A | T | 3 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 |
4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2069-303T>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493409 | |||||||
chr7:1493415 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2069-309C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493415 | |||||||
chr7:1493458 | G | A | 8 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(5): Show |
11 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2068+296C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493458 | |||||||
chr7:1493487 | G | A | 1 | a0001c0020t0002g0104 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2068+267C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493487 | |||||||
chr7:1493493 | T | G | 8 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(5): Show |
11 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2068+261A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493493 | |||||||
chr7:1493500 | G | A | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2068+254C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493500 | |||||||
chr7:1493502 | G | A | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2068+252C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493502 | |||||||
chr7:1493558 | T | C | 1 | a0001c0036t0012g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2068+196A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493558 | |||||||
chr7:1493574 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0150 a0001c0001t0001g0204 |
4 | HG02723.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+180G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493574 | |||||||
chr7:1493591 | C | CG | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2068+162dupC | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493591 | |||||||
chr7:1493613 | TC | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.2068+140delG | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493613 | |||||||
chr7:1493657 | T | C | 2 | a0001c0008t0004g0019 a0001c0008t0007g0044 |
3 | HG02738.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2068+97A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493657 | |||||||
chr7:1493672 | G | A | 6 | a0001c0002t0002g0081 a0001c0002t0002g0082 a0001c0002t0002g0092 others(3): Show |
6 | HG02027.hp1 HG02040.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2068+82C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493672 | |||||||
chr7:1493706 | C | T | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2068+48G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493706 | |||||||
chr7:1493717 | G | C | 2 | a0001c0008t0004g0019 a0001c0008t0007g0044 |
3 | HG02738.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2068+37C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493717 | |||||||
chr7:1493920 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1911-9A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1493920 | |||||||
chr7:1493925 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1911-14C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1493925 | |||||||
chr7:1493930 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1911-19T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1493930 | |||||||
chr7:1493930 | A | T | 1 | a0001c0005t0001g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1911-19T>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1493930 | |||||||
chr7:1493974 | G | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0122 others(14): Show |
26 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.1911-63C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1493974 | |||||||
chr7:1494005 | C | T | 1 | a0001c0002t0002g0083 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1911-94G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494005 | |||||||
chr7:1494028 | G | A | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1911-117C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494028 | |||||||
chr7:1494152 | A | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1911-241T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494152 | |||||||
chr7:1494206 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG00621.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1911-295T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494206 | |||||||
chr7:1494230 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1911-319G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494230 | |||||||
chr7:1494254 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1911-343C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494254 | |||||||
chr7:1494316 | C | T | 2 | a0001c0009t0001g0042 a0001c0009t0001g0218 |
3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1911-405G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494316 | |||||||
chr7:1494317 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1911-406C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494317 | |||||||
chr7:1494328 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1911-417C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494328 | |||||||
chr7:1494374 | G | A | 1 | a0013c0046t0001g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1910+442C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494374 | |||||||
chr7:1494397 | C | A | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1910+419G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494397 | |||||||
chr7:1494409 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1910+407A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494409 | |||||||
chr7:1494431 | C | T | 8 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(5): Show |
11 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1910+385G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494431 | |||||||
chr7:1494510 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1910+306G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494510 | |||||||
chr7:1494519 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1910+297A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494519 | |||||||
chr7:1494523 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0184 |
4 | HG01891.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1910+293C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494523 | |||||||
chr7:1494597 | T | C | 1 | a0001c0038t0001g0116 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1910+219A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494597 | |||||||
chr7:1494620 | C | T | 1 | a0001c0002t0002g0092 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1910+196G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494620 | |||||||
chr7:1494622 | T | A | 1 | a0015c0045t0001g0179 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1910+194A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494622 | |||||||
chr7:1494733 | G | T | 1 | a0001c0041t0006g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1910+83C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494733 | |||||||
chr7:1494735 | C | G | 1 | a0001c0041t0006g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1910+81G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494735 | |||||||
chr7:1494738 | T | C | 1 | a0001c0041t0006g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1910+78A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494738 | |||||||
chr7:1494789 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1910+27T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494789 | |||||||
chr7:1494950 | G | A | 1 | a0001c0047t0001g0176 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1833-57C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1494950 | |||||||
chr7:1494957 | C | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1833-64G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1494957 | |||||||
chr7:1495067 | C | T | 1 | a0001c0002t0002g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1833-174G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495067 | |||||||
chr7:1495083 | C | G | 9 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(6): Show |
12 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1833-190G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495083 | |||||||
chr7:1495088 | C | A | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1833-195G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495088 | |||||||
chr7:1495099 | G | T | 1 | a0007c0024t0002g0063 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1833-206C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495099 | |||||||
chr7:1495115 | A | AGTGGCCG others(3): Show |
152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1833-223_1833-222i others(12): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495115 | |||||||
chr7:1495116 | G | GTGGCCGA others(3): Show |
2 | a0001c0001t0001g0177 a0016c0030t0001g0141 |
2 | NA18950.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1833-224_1833-223i others(12): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495116 | |||||||
chr7:1495231 | C | T | 4 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(1): Show |
4 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1832+202G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495231 | |||||||
chr7:1495259 | A | T | 9 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(6): Show |
12 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1832+174T>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495259 | |||||||
chr7:1495321 | G | T | 1 | a0001c0041t0006g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1832+112C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495321 | |||||||
chr7:1495351 | T | G | 9 | a0001c0002t0002g0004 a0001c0002t0002g0010 a0001c0002t0002g0025 others(6): Show |
18 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1832+82A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495351 | |||||||
chr7:1495415 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1832+18T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495415 | |||||||
chr7:1495619 | G | A | 1 | a0018c0040t0003g0178 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1712-66C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495619 | |||||||
chr7:1495636 | C | G | 1 | a0001c0002t0002g0085 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1712-83G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495636 | |||||||
chr7:1495761 | G | A | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1712-208C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495761 | |||||||
chr7:1495787 | A | G | 1 | a0001c0002t0002g0085 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1712-234T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495787 | |||||||
chr7:1495799 | C | A | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1712-246G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495799 | |||||||
chr7:1495952 | AG | A | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1711+203delC | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495952 | |||||||
chr7:1495996 | C | G | 1 | a0008c0032t0003g0190 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1711+160G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495996 | |||||||
chr7:1495996 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1711+160G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495996 | |||||||
chr7:1496031 | T | C | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1711+125A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1496031 | |||||||
chr7:1496116 | A | G | 3 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 |
4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1711+40T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1496116 | |||||||
chr7:1496136 | G | C | 1 | a0001c0002t0002g0085 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1711+20C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1496136 | |||||||
chr7:1496275 | A | AGCACGGG others(54): Show |
4 | a0001c0005t0001g0138 a0001c0005t0001g0139 a0001c0036t0012g0224 others(1): Show |
4 | HG00280.hp2 HG01175.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-72_1603-12dup others(61): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496275 | |||||||
chr7:1496275 | A | AGCATGGG others(54): Show |
1 | a0001c0020t0002g0104 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1603-12_1603-11ins others(61): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496275 | |||||||
chr7:1496275 | AGCACGGG others(54): Show |
A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1603-72_1603-12del others(61): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496275 | |||||||
chr7:1496275 | AGCACGGG others(115): Show |
A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG00621.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1603-133_1603-12de others(1): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496275 | |||||||
chr7:1496279 | C | T | 1 | a0001c0019t0002g0105 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1603-15G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496279 | |||||||
chr7:1496330 | G | GGGCGCGG others(53): Show |
1 | a0001c0019t0002g0105 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1603-126_1603-67du others(61): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496330 | |||||||
chr7:1496344 | G | A | 1 | a0001c0002t0002g0086 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1603-80C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496344 | |||||||
chr7:1496445 | C | A | 1 | a0015c0045t0001g0179 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1603-181G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496445 | |||||||
chr7:1496446 | C | CCACGTGG others(54): Show |
3 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 |
4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-243_1603-183d others(63): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496446 | |||||||
chr7:1496449 | C | A | 5 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(2): Show |
5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1603-185G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496449 | |||||||
chr7:1496450 | G | T | 1 | a0001c0041t0006g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1603-186C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496450 | |||||||
chr7:1496700 | G | A | 21 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(18): Show |
27 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1603-436C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496700 | |||||||
chr7:1496753 | A | G | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1602+385T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496753 | |||||||
chr7:1496800 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1602+338T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496800 | |||||||
chr7:1496812 | A | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1602+326T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496812 | |||||||
chr7:1496930 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1602+208A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496930 | |||||||
chr7:1496947 | G | T | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1602+191C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496947 | |||||||
chr7:1496987 | G | A | 17 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0133 others(14): Show |
21 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1602+151C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496987 | |||||||
chr7:1496992 | A | C | 1 | a0001c0041t0006g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1602+146T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496992 | |||||||
chr7:1496993 | C | A | 1 | a0001c0041t0006g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1602+145G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496993 | |||||||
chr7:1496994 | C | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(148): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1602+144G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496994 | |||||||
chr7:1496996 | C | G | 1 | a0001c0041t0006g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1602+142G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496996 | |||||||
chr7:1496997 | A | C | 1 | a0001c0041t0006g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1602+141T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496997 | |||||||
chr7:1497081 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1602+57A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1497081 | |||||||
chr7:1497087 | C | T | 1 | a0001c0002t0002g0062 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1602+51G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1497087 | |||||||
chr7:1497333 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1426-19C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497333 | |||||||
chr7:1497439 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1426-125A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497439 | |||||||
chr7:1497449 | C | T | 1 | a0001c0002t0002g0020 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1426-135G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497449 | |||||||
chr7:1497576 | G | T | 2 | a0001c0008t0004g0019 a0001c0008t0007g0044 |
3 | HG02738.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1426-262C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497576 | |||||||
chr7:1497594 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1426-280C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497594 | |||||||
chr7:1497705 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1426-391A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497705 | |||||||
chr7:1497776 | C | T | 1 | a0001c0023t0002g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1426-462G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497776 | |||||||
chr7:1497777 | T | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1426-463A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497777 | |||||||
chr7:1497781 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1426-467A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497781 | |||||||
chr7:1497789 | A | G | 15 | a0001c0003t0001g0030 a0001c0003t0001g0039 a0001c0003t0001g0041 others(12): Show |
19 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1426-475T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497789 | |||||||
chr7:1497803 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1426-489A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497803 | |||||||
chr7:1497826 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1426-512G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497826 | |||||||
chr7:1497941 | C | A | 1 | a0001c0002t0002g0087 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1425+471G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497941 | |||||||
chr7:1498042 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1425+370C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498042 | |||||||
chr7:1498050 | C | CA | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1425+361dupT | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498050 | |||||||
chr7:1498055 | T | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1425+357A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498055 | |||||||
chr7:1498065 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1425+347G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498065 | |||||||
chr7:1498068 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1425+344G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498068 | |||||||
chr7:1498091 | G | C | 1 | a0001c0036t0012g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1425+321C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498091 | |||||||
chr7:1498250 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1425+162T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498250 | |||||||
chr7:1498287 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0215 |
2 | HG02132.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1425+125C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498287 | |||||||
chr7:1498296 | G | T | 1 | a0001c0002t0002g0061 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1425+116C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498296 | |||||||
chr7:1498302 | T | C | 2 | a0001c0019t0002g0105 a0001c0020t0002g0104 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1425+110A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498302 | |||||||
chr7:1498385 | G | A | 2 | a0001c0002t0002g0026 a0001c0002t0002g0088 |
3 | HG01167.hp1 HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1425+27C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498385 | |||||||
chr7:1498389 | A | G | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1425+23T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498389 | |||||||
chr7:1498570 | TAC | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0205 |
3 | HG02559.hp1 HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1284-19_1284-18del others(2): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/47 | chr7 | 1498570 | |||||||
chr7:1498572 | C | T | 1 | a0001c0002t0002g0073 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1284-19G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/47 | chr7 | 1498572 | |||||||
chr7:1498589 | ACGCCTGT others(10): Show |
A | 5 | a0001c0018t0004g0109 a0001c0021t0004g0110 a0001c0022t0004g0111 others(2): Show |
6 | HG02280.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284-53_1284-37del others(17): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/47 | chr7 | 1498589 | |||||||
chr7:1498642 | GCCCACAC others(5): Show |
G | 1 | a0001c0001t0002g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1283+53_1283+64del others(12): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/47 | chr7 | 1498642 | |||||||
chr7:1498644 | C | T | 1 | a0001c0035t0001g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1283+63G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/47 | chr7 | 1498644 | |||||||
chr7:1498863 | G | C | 5 | a0001c0002t0002g0027 a0001c0002t0002g0090 a0001c0002t0002g0095 others(2): Show |
6 | HG01891.hp1 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1138-11C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/47 | chr7 | 1498863 | |||||||
chr7:1498896 | C | G | 1 | a0001c0001t0001g0016 | 3 | HG00438.hp1 HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1138-44G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/47 | chr7 | 1498896 | |||||||
chr7:1498903 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1138-51T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/47 | chr7 | 1498903 | |||||||
chr7:1498907 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1138-55G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/47 | chr7 | 1498907 | |||||||
chr7:1498959 | C | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1137+16G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/47 | chr7 | 1498959 | |||||||
chr7:1498959 | C | G | 1 | a0008c0032t0003g0190 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1137+16G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/47 | chr7 | 1498959 | |||||||
chr7:1499181 | G | A | 1 | a0001c0023t0002g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.951-20C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/47 | chr7 | 1499181 | |||||||
chr7:1499208 | G | A | 1 | a0001c0005t0001g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.950+47C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/47 | chr7 | 1499208 | |||||||
chr7:1499212 | G | GC | 17 | a0001c0001t0001g0114 a0001c0001t0001g0192 a0001c0001t0001g0193 others(14): Show |
18 | HG00280.hp2 HG00544.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.950+42dupG | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/47 | chr7 | 1499212 | |||||||
chr7:1499217 | C | T | 1 | a0001c0035t0001g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.950+38G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/47 | chr7 | 1499217 | |||||||
chr7:1499241 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.950+14T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/47 | chr7 | 1499241 | |||||||
chr7:1499406 | AT | A | 5 | a0001c0018t0004g0109 a0001c0021t0004g0110 a0001c0022t0004g0111 others(2): Show |
6 | HG02280.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.845-47delA | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 6/47 | chr7 | 1499406 | |||||||
chr7:1499462 | G | A | 1 | a0001c0002t0002g0097 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.844+11C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 6/47 | chr7 | 1499462 | |||||||
chr7:1499670 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.685-38C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 5/47 | chr7 | 1499670 | |||||||
chr7:1499760 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.684+124C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 5/47 | chr7 | 1499760 | |||||||
chr7:1499836 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.684+48T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 5/47 | chr7 | 1499836 | |||||||
chr7:1499843 | G | C | 1 | a0001c0036t0012g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.684+41C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 5/47 | chr7 | 1499843 | |||||||
chr7:1499845 | C | T | 1 | a0001c0036t0012g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.684+39G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 5/47 | chr7 | 1499845 | |||||||
chr7:1500045 | G | A | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.547-24C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 4/47 | chr7 | 1500045 | |||||||
chr7:1500163 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
splice_region_variant&intron_variant | LOW | c.546+7G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 4/47 | chr7 | 1500163 | |||||||
chr7:1500382 | G | A | 1 | a0001c0002t0002g0099 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.350-16C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500382 | |||||||
chr7:1500413 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.350-47T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500413 | |||||||
chr7:1500463 | A | G | 3 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 |
4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-97T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500463 | |||||||
chr7:1500512 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.350-146G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500512 | |||||||
chr7:1500530 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.350-164G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500530 | |||||||
chr7:1500644 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.350-278A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500644 | |||||||
chr7:1500679 | T | C | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.350-313A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500679 | |||||||
chr7:1500698 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.350-332C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500698 | |||||||
chr7:1500731 | C | G | 2 | a0001c0002t0002g0013 a0001c0010t0001g0031 |
5 | HG01167.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-365G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500731 | |||||||
chr7:1500749 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG00621.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.350-383C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500749 | |||||||
chr7:1500814 | T | G | 9 | a0001c0001t0002g0106 a0001c0008t0004g0019 a0001c0008t0007g0044 others(6): Show |
11 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.350-448A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500814 | |||||||
chr7:1500866 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.350-500A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500866 | |||||||
chr7:1500869 | G | A | 3 | a0001c0002t0002g0100 a0001c0002t0002g0102 a0001c0002t0009g0101 |
3 | HG00735.hp2 HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.350-503C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500869 | |||||||
chr7:1500899 | A | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.350-533T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500899 | |||||||
chr7:1500905 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.350-539C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500905 | |||||||
chr7:1500955 | C | T | 6 | a0001c0005t0001g0138 a0001c0005t0001g0139 a0001c0006t0005g0043 others(3): Show |
7 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-589G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500955 | |||||||
chr7:1500977 | G | C | 1 | a0001c0002t0002g0103 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.350-611C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500977 | |||||||
chr7:1501002 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.350-636G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501002 | |||||||
chr7:1501209 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.350-843G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501209 | |||||||
chr7:1501227 | G | A | 1 | a0001c0042t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.350-861C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501227 | |||||||
chr7:1501284 | CAA | C | 4 | a0001c0001t0001g0136 a0001c0011t0001g0040 a0001c0011t0001g0208 others(1): Show |
5 | HG00639.hp1 HG01081.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-920_350-919del others(2): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501284 | |||||||
chr7:1501292 | AAT | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.350-928_350-927del others(2): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501292 | |||||||
chr7:1501293 | AT | A | 3 | a0001c0019t0002g0105 a0001c0020t0002g0104 a0008c0032t0003g0190 |
3 | HG01109.hp2 HG02056.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.350-928delA | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501293 | |||||||
chr7:1501294 | T | A | 1 | a0001c0002t0002g0080 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.350-928A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501294 | |||||||
chr7:1501298 | T | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.350-932A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501298 | |||||||
chr7:1501366 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.350-1000A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501366 | |||||||
chr7:1501516 | A | G | 1 | a0001c0002t0002g0055 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.350-1150T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501516 | |||||||
chr7:1501555 | A | G | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.350-1189T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501555 | |||||||
chr7:1501562 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0019c0043t0001g0113 |
3 | NA19009.hp1 NA19081.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.350-1196G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501562 | |||||||
chr7:1501621 | G | A | 1 | a0001c0036t0012g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.350-1255C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501621 | |||||||
chr7:1501626 | G | C | 1 | a0001c0002t0002g0048 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.350-1260C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501626 | |||||||
chr7:1501640 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02630.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.349+1261G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501640 | |||||||
chr7:1501801 | C | G | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.349+1100G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501801 | |||||||
chr7:1501811 | C | G | 1 | a0001c0005t0001g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.349+1090G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501811 | |||||||
chr7:1501847 | C | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.349+1054G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501847 | |||||||
chr7:1501852 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.349+1049C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501852 | |||||||
chr7:1501933 | T | G | 2 | a0001c0001t0001g0129 a0001c0041t0006g0045 |
2 | NA19068.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.349+968A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501933 | |||||||
chr7:1501993 | C | A | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+908G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501993 | |||||||
chr7:1501994 | C | G | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+907G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501994 | |||||||
chr7:1502070 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.349+831C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502070 | |||||||
chr7:1502202 | C | T | 6 | a0001c0002t0002g0002 a0001c0002t0002g0050 a0001c0002t0002g0051 others(3): Show |
11 | HG01255.hp1 HG01258.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.349+699G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502202 | |||||||
chr7:1502244 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.349+657A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502244 | |||||||
chr7:1502362 | G | A | 6 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+539C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502362 | |||||||
chr7:1502413 | G | A | 2 | a0001c0011t0001g0040 a0001c0011t0001g0208 |
3 | HG00639.hp1 HG01081.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.349+488C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502413 | |||||||
chr7:1502488 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.349+413C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502488 | |||||||
chr7:1502489 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.349+412T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502489 | |||||||
chr7:1502492 | G | A | 1 | a0001c0038t0001g0116 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.349+409C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502492 | |||||||
chr7:1502591 | C | T | 7 | a0001c0008t0004g0019 a0001c0008t0007g0044 a0001c0018t0004g0109 others(4): Show |
9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+310G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502591 | |||||||
chr7:1502658 | C | A | 2 | a0001c0009t0001g0042 a0001c0009t0001g0218 |
3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.349+243G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502658 | |||||||
chr7:1502691 | G | A | 1 | a0009c0033t0010g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.349+210C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502691 | |||||||
chr7:1502773 | A | C | 7 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(4): Show |
7 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+128T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502773 | |||||||
chr7:1502798 | C | T | 3 | a0001c0001t0001g0130 a0001c0009t0001g0042 a0001c0009t0001g0218 |
4 | HG02895.hp1 HG03130.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+103G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502798 | |||||||
chr7:1502830 | G | A | 3 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 |
4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+71C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502830 | |||||||
chr7:1502854 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
6 | HG00140.hp1 HG00280.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+47C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502854 | |||||||
chr7:1502869 | G | T | 1 | a0001c0002t0002g0049 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.349+32C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502869 | |||||||
chr7:1503279 | G | A | 5 | a0001c0005t0001g0117 a0001c0005t0001g0212 a0001c0005t0001g0213 others(2): Show |
5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-88C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503279 | |||||||
chr7:1503302 | G | A | 1 | a0001c0003t0001g0041 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.59-111C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503302 | |||||||
chr7:1503344 | C | T | 2 | a0001c0001t0001g0129 a0001c0041t0006g0045 |
2 | NA19068.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.59-153G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503344 | |||||||
chr7:1503563 | G | T | 1 | a0001c0002t0002g0048 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.58+340C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503563 | |||||||
chr7:1503652 | G | C | 1 | a0001c0020t0002g0104 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.58+251C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503652 | |||||||
chr7:1503663 | T | C | 1 | a0001c0034t0002g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.58+240A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503663 | |||||||
chr7:1503756 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.58+147C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503756 | |||||||
chr7:1503799 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0127 a0001c0001t0001g0128 |
4 | HG00140.hp1 HG00280.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+104G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503799 | |||||||
chr7:1503840 | T | TCCCCAAA others(3): Show |
125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.58+53_58+62dupGTCT others(6): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503840 | |||||||
chr7:1503840 | T | TCCCCAAA others(13): Show |
2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.58+43_58+62dupGTCT others(16): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503840 | |||||||
chr7:1503840 | T | TTCCCAAA others(3): Show |
2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | NA18959.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.58+62_58+63insGTCT others(6): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503840 | |||||||
chr7:1503840 | TCCCCAAA others(3): Show |
T | 3 | a0001c0005t0001g0117 a0001c0034t0002g0047 a0001c0038t0001g0116 |
3 | HG02897.hp1 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.58+53_58+62delGTCT others(6): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503840 | |||||||
chr7:1504007 | G | A | 1 | a0001c0002t0002g0015 | 3 | HG01069.hp1 HG01071.hp2 HG01175.hp1 |
splice_region_variant&intron_variant | LOW | c.-41-6C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504007 | |||||||
chr7:1504012 | G | A | 2 | a0001c0009t0001g0042 a0001c0009t0001g0218 |
3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-41-11C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504012 | |||||||
chr7:1504084 | G | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0019c0043t0001g0113 |
3 | NA19009.hp1 NA19081.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-41-83C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504084 | |||||||
chr7:1504093 | AC | A | 4 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG01496.hp2 HG02055.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41-93delG | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504093 | |||||||
chr7:1504098 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-41-97C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504098 | |||||||
chr7:1504105 | T | G | 5 | a0001c0018t0004g0109 a0001c0021t0004g0110 a0001c0022t0004g0111 others(2): Show |
6 | HG02280.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41-104A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504105 | |||||||
chr7:1504173 | G | A | 4 | a0001c0006t0005g0043 a0001c0006t0005g0225 a0001c0006t0005g0226 others(1): Show |
5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42+150C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504173 |