Item | Value |
---|---|
geneid | 55821 |
ensemblid | ENSG00000151360.10 |
hgncid | 17377 |
symbol | ALLC |
name | allantoicase |
refseq_nuc | NM_018436.4 |
refseq_prot | NP_060906.3 |
ensembl_nuc | ENST00000252505.4 |
ensembl_prot | ENSP00000252505.3 |
mane_status | MANE Select |
chr | chr2 |
start | 3658200 |
end | 3702671 |
strand | + |
ver | v1.2 |
region | chr2:3658200-3702671 |
region5000 | chr2:3653200-3707671 |
regionname0 | ALLC_chr2_3658200_3702671 |
regionname5000 | ALLC_chr2_3653200_3707671 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 391 | 117 | 25 | 34 | 45 | 4 | 8 | 37 | ALLC_chr2_3653200_3707671 | ALLC | MDMAS others(386): Show |
chr2 | 3653200 | 3707671 |
a0002 | 0/0 | 390 | 74 | 25 | 12 | 26 | 4 | 7 | 18 | ALLC_chr2_3653200_3707671 | ALLC | MDMAS others(385): Show |
chr2 | 3653200 | 3707671 |
a0003 | 0/1 | 390 | 60 | 23 | 15 | 14 | 4 | 3 | 9 | ALLC_chr2_3653200_3707671 | ALLC | MDMAS others(385): Show |
chr2 | 3653200 | 3707671 |
a0004 | 0/0 | 391 | 16 | 8 | 0 | 8 | 0 | 0 | 3 | ALLC_chr2_3653200_3707671 | ALLC | MDMAS others(386): Show |
chr2 | 3653200 | 3707671 |
a0005 | 0/0 | 390 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | MDMAS others(385): Show |
chr2 | 3653200 | 3707671 |
a0006 | 0/0 | 390 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | MDMAS others(385): Show |
chr2 | 3653200 | 3707671 |
a0007 | 0/0 | 390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | MDMAS others(385): Show |
chr2 | 3653200 | 3707671 |
a0008 | 0/0 | 100 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALLC_chr2_3653200_3707671 | ALLC | MDMAS others(95): Show |
chr2 | 3653200 | 3707671 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1173 | 116 | 25 | 34 | 44 | 4 | 8 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1168): Show |
chr2 | 3653200 | 3707671 | ||
a0001c0012 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1168): Show |
chr2 | 3653200 | 3707671 | ||
a0002c0002 | 0/0 | 1170 | 61 | 13 | 12 | 25 | 4 | 7 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1165): Show |
chr2 | 3653200 | 3707671 | ||
a0002c0005 | 0/0 | 1170 | 6 | 6 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1165): Show |
chr2 | 3653200 | 3707671 | ||
a0002c0006 | 0/0 | 1170 | 3 | 3 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1165): Show |
chr2 | 3653200 | 3707671 | ||
a0002c0009 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1165): Show |
chr2 | 3653200 | 3707671 | ||
a0002c0013 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1165): Show |
chr2 | 3653200 | 3707671 | ||
a0002c0014 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1165): Show |
chr2 | 3653200 | 3707671 | ||
a0002c0015 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1165): Show |
chr2 | 3653200 | 3707671 | ||
a0003c0003 | 0/1 | 1170 | 59 | 22 | 15 | 14 | 4 | 3 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1165): Show |
chr2 | 3653200 | 3707671 | ||
a0003c0010 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1165): Show |
chr2 | 3653200 | 3707671 | ||
a0004c0004 | 0/0 | 1173 | 16 | 8 | 0 | 8 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1168): Show |
chr2 | 3653200 | 3707671 | ||
a0005c0007 | 0/0 | 1170 | 3 | 2 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1165): Show |
chr2 | 3653200 | 3707671 | ||
a0006c0008 | 0/0 | 1170 | 2 | 2 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1165): Show |
chr2 | 3653200 | 3707671 | ||
a0007c0011 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1165): Show |
chr2 | 3653200 | 3707671 | ||
a0008c0016 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATGGA others(1165): Show |
chr2 | 3653200 | 3707671 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1441 | 96 | 19 | 32 | 35 | 4 | 5 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1436): Show |
chr2 | 3653200 | 3707671 |
a0001c0001t0002 | 0/0 | 1441 | 17 | 4 | 2 | 8 | 0 | 3 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1436): Show |
chr2 | 3653200 | 3707671 |
a0001c0001t0003 | 0/0 | 1441 | 2 | 2 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1436): Show |
chr2 | 3653200 | 3707671 |
a0001c0001t0005 | 0/0 | 1416 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1411): Show |
chr2 | 3653200 | 3707671 |
a0001c0012t0002 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1436): Show |
chr2 | 3653200 | 3707671 |
a0002c0002t0001 | 0/0 | 1438 | 14 | 2 | 3 | 7 | 2 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0002c0002t0002 | 0/0 | 1438 | 47 | 11 | 9 | 18 | 2 | 7 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0002c0005t0001 | 0/0 | 1438 | 4 | 4 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0002c0005t0002 | 0/0 | 1438 | 2 | 2 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0002c0006t0001 | 0/0 | 1438 | 2 | 2 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0002c0006t0002 | 0/0 | 1438 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0002c0009t0002 | 0/0 | 1438 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0002c0013t0002 | 0/0 | 1438 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0002c0014t0002 | 0/0 | 1438 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0002c0015t0002 | 0/0 | 1438 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0003c0003t0001 | 0/0 | 1438 | 16 | 2 | 7 | 4 | 2 | 1 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0003c0003t0002 | 0/1 | 1438 | 43 | 20 | 8 | 10 | 2 | 2 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0003c0010t0004 | 0/0 | 1438 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0004c0004t0001 | 0/0 | 1441 | 7 | 5 | 0 | 2 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1436): Show |
chr2 | 3653200 | 3707671 |
a0004c0004t0002 | 0/0 | 1441 | 7 | 1 | 0 | 6 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1436): Show |
chr2 | 3653200 | 3707671 |
a0004c0004t0003 | 0/0 | 1441 | 2 | 2 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1436): Show |
chr2 | 3653200 | 3707671 |
a0005c0007t0004 | 0/0 | 1438 | 3 | 2 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0006c0008t0002 | 0/0 | 1438 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0006c0008t0003 | 0/0 | 1438 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0007c0011t0001 | 0/0 | 1438 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
a0008c0016t0002 | 0/0 | 1438 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | ATTCT others(1433): Show |
chr2 | 3653200 | 3707671 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 13 | 0 | 2 | 6 | 2 | 3 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0001c0012t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0005t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0005t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0005t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0005t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0006t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0006t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0009t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0013t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0014t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0002c0015t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0005 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0003c0010t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0004c0004t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0005c0007t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0005c0007t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0005c0007t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0006c0008t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0006c0008t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0007c0011t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
a0008c0016t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0002 | c0002 | t0002 | g0105 | EUR | FIN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0096 | EUR | FIN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00323 | hp2 | a0003 | c0003 | t0001 | g0005 | EUR | FIN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00408 | hp1 | a0004 | c0004 | t0002 | g0173 | EAS | CHS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | CHS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0090 | EAS | CHS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00423 | hp2 | a0004 | c0004 | t0002 | g0165 | EAS | CHS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | CHS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00558 | hp2 | a0004 | c0004 | t0001 | g0198 | EAS | CHS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | CHS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0139 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00642 | hp1 | a0003 | c0003 | t0001 | g0119 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0191 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00735 | hp2 | a0003 | c0003 | t0002 | g0136 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG00741 | hp2 | a0003 | c0003 | t0001 | g0117 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01070 | hp1 | a0003 | c0003 | t0002 | g0016 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01071 | hp1 | a0003 | c0003 | t0002 | g0016 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0062 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01081 | hp2 | a0003 | c0003 | t0002 | g0183 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01106 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0151 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01168 | hp2 | a0003 | c0003 | t0001 | g0116 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01169 | hp1 | a0003 | c0003 | t0001 | g0052 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01243 | hp2 | a0003 | c0003 | t0002 | g0006 | AMR | PUR | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01256 | hp2 | a0003 | c0003 | t0002 | g0014 | AMR | CLM | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01258 | hp2 | a0003 | c0003 | t0002 | g0014 | AMR | CLM | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01346 | hp1 | a0003 | c0003 | t0002 | g0193 | AMR | CLM | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0156 | AMR | CLM | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01361 | hp2 | a0003 | c0003 | t0001 | g0065 | AMR | CLM | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0186 | EUR | IBS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01516 | hp1 | a0003 | c0003 | t0002 | g0017 | EUR | IBS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01516 | hp2 | a0003 | c0003 | t0001 | g0115 | EUR | IBS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01517 | hp2 | a0003 | c0003 | t0002 | g0017 | EUR | IBS | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01891 | hp1 | a0003 | c0003 | t0002 | g0033 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01891 | hp2 | a0003 | c0003 | t0002 | g0221 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0106 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0061 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0081 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0194 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02055 | hp1 | a0003 | c0003 | t0002 | g0028 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02056 | hp2 | a0003 | c0003 | t0002 | g0178 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02071 | hp1 | a0003 | c0003 | t0001 | g0200 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02080 | hp2 | a0003 | c0003 | t0002 | g0018 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02083 | hp2 | a0003 | c0003 | t0001 | g0098 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02145 | hp2 | a0002 | c0002 | t0002 | g0210 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02148 | hp2 | a0003 | c0003 | t0001 | g0201 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02155 | hp1 | a0004 | c0004 | t0002 | g0170 | EAS | CDX | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CDX | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02257 | hp1 | a0004 | c0004 | t0001 | g0035 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02257 | hp2 | a0003 | c0003 | t0002 | g0159 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02258 | hp1 | a0003 | c0003 | t0002 | g0042 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02258 | hp2 | a0004 | c0004 | t0001 | g0137 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02280 | hp1 | a0003 | c0003 | t0002 | g0006 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02451 | hp1 | a0003 | c0003 | t0002 | g0030 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02451 | hp2 | a0002 | c0002 | t0002 | g0162 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02523 | hp1 | a0004 | c0004 | t0001 | g0079 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02523 | hp2 | a0003 | c0003 | t0002 | g0171 | EAS | KHV | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0024 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02647 | hp1 | a0002 | c0005 | t0001 | g0215 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0213 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02717 | hp1 | a0006 | c0008 | t0002 | g0181 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02717 | hp2 | a0003 | c0003 | t0002 | g0039 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02723 | hp1 | a0004 | c0004 | t0003 | g0224 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02723 | hp2 | a0005 | c0007 | t0004 | g0226 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02738 | hp1 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02738 | hp2 | a0003 | c0003 | t0002 | g0163 | SAS | PJL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0133 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02809 | hp2 | a0003 | c0003 | t0002 | g0015 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02818 | hp1 | a0002 | c0005 | t0001 | g0208 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02818 | hp2 | a0002 | c0002 | t0002 | g0134 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02886 | hp1 | a0002 | c0009 | t0002 | g0023 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0152 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02895 | hp1 | a0003 | c0003 | t0002 | g0048 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02896 | hp1 | a0003 | c0003 | t0002 | g0027 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02897 | hp2 | a0003 | c0003 | t0002 | g0026 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02922 | hp1 | a0003 | c0003 | t0002 | g0015 | AFR | ESN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02922 | hp2 | a0002 | c0006 | t0002 | g0135 | AFR | ESN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02970 | hp1 | a0002 | c0005 | t0002 | g0022 | AFR | ESN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03041 | hp1 | a0002 | c0014 | t0002 | g0218 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03130 | hp1 | a0003 | c0003 | t0002 | g0043 | AFR | ESN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03130 | hp2 | a0004 | c0004 | t0001 | g0036 | AFR | ESN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0212 | AFR | ESN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03139 | hp2 | a0003 | c0003 | t0002 | g0211 | AFR | ESN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | ESN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0142 | AFR | ESN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0209 | AFR | MSL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0214 | AFR | MSL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03453 | hp2 | a0002 | c0006 | t0001 | g0141 | AFR | MSL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03486 | hp2 | a0003 | c0003 | t0002 | g0150 | AFR | MSL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03516 | hp1 | a0004 | c0004 | t0001 | g0045 | AFR | ESN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03540 | hp1 | a0002 | c0005 | t0001 | g0206 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03579 | hp1 | a0003 | c0003 | t0002 | g0122 | AFR | MSL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03579 | hp2 | a0003 | c0003 | t0001 | g0038 | AFR | MSL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0060 | SAS | PJL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | STU | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0149 | SAS | STU | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03704 | hp2 | a0003 | c0003 | t0002 | g0153 | SAS | PJL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | STU | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | STU | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0155 | SAS | STU | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0157 | SAS | STU | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18522 | hp1 | a0004 | c0004 | t0003 | g0223 | AFR | YRI | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18522 | hp2 | a0002 | c0005 | t0001 | g0207 | AFR | YRI | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18906 | hp1 | a0006 | c0008 | t0003 | g0231 | AFR | YRI | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18906 | hp2 | a0003 | c0003 | t0002 | g0032 | AFR | YRI | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18942 | hp1 | a0002 | c0015 | t0002 | g0059 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18942 | hp2 | a0001 | c0012 | t0002 | g0216 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18952 | hp2 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18961 | hp2 | a0004 | c0004 | t0002 | g0180 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18969 | hp1 | a0003 | c0003 | t0002 | g0177 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18971 | hp2 | a0004 | c0004 | t0002 | g0174 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18995 | hp1 | a0003 | c0003 | t0002 | g0179 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19007 | hp2 | a0003 | c0003 | t0002 | g0176 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0205 | AFR | LWK | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19043 | hp2 | a0002 | c0005 | t0002 | g0047 | AFR | LWK | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19054 | hp1 | a0003 | c0003 | t0002 | g0169 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19063 | hp1 | a0003 | c0003 | t0001 | g0053 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19066 | hp2 | a0003 | c0003 | t0002 | g0168 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19068 | hp1 | a0004 | c0004 | t0002 | g0164 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19074 | hp2 | a0003 | c0003 | t0002 | g0172 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19082 | hp2 | a0008 | c0016 | t0002 | g0160 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19088 | hp1 | a0003 | c0003 | t0001 | g0097 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19240 | hp1 | a0002 | c0013 | t0002 | g0031 | AFR | YRI | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA20129 | hp1 | a0004 | c0004 | t0002 | g0110 | AFR | ASW | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA20129 | hp2 | a0004 | c0004 | t0001 | g0037 | AFR | ASW | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0085 | EUR | TSI | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0128 | AMR | CLM | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG01123 | hp2 | a0005 | c0007 | t0004 | g0225 | AMR | CLM | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0222 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02486 | hp1 | a0007 | c0011 | t0001 | g0124 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG02559 | hp2 | a0005 | c0007 | t0004 | g0229 | AFR | ACB | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03471 | hp1 | a0003 | c0003 | t0002 | g0158 | AFR | MSL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG03471 | hp2 | a0002 | c0006 | t0001 | g0041 | AFR | MSL | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | USA | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA20300 | hp1 | a0003 | c0003 | t0002 | g0123 | AFR | USA | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | USA | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA21309 | hp1 | a0003 | c0010 | t0004 | g0228 | AFR | LWK | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
NA21309 | hp2 | a0003 | c0003 | t0001 | g0120 | AFR | LWK | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
homoSapiens | chm13v2 | a0003 | c0003 | t0002 | g0167 | REF | REF | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0082 | REF | REF | ALLC_chr2_3653200_3707671 | ALLC | chr2 | 3653200 | 3707671 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:3678516 | T | C | 1 | a0007 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.133T>C | p.Trp45Arg | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/12 | 290/1441 | 133/1176 | 45/391 | chr2 | 3678516 | |||
chr2:3681636 | A | T | 1 | a0008 | 1 | NA19082.hp2 | stop_gained&splice_region_variant | HIGH | c.301A>T | p.Lys101* | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/12 | 458/1441 | 301/1176 | 101/391 | chr2 | 3681636 | |||
chr2:3681664 | C | T | 4 | a0003 a0004 a0005 others(1): Show |
80 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
missense_variant | MODERATE | c.329C>T | p.Thr110Ile | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/12 | 486/1441 | 329/1176 | 110/391 | chr2 | 3681664 | |||
chr2:3681713 | G | T | 1 | a0008 | 1 | NA19082.hp2 | missense_variant&splice_region_variant | MODERATE | c.378G>T | p.Glu126Asp | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/12 | 535/1441 | 378/1176 | 126/391 | chr2 | 3681713 | |||
chr2:3697400 | G | A | 1 | a0005 | 3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
missense_variant | MODERATE | c.794G>A | p.Arg265Gln | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/12 | 951/1441 | 794/1176 | 265/391 | chr2 | 3697400 | |||
chr2:3701529 | T | C | 2 | a0005 a0006 |
5 | HG01123.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
missense_variant | MODERATE | c.868T>C | p.Cys290Arg | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 11/12 | 1025/1441 | 868/1176 | 290/391 | chr2 | 3701529 | |||
chr2:3701561 | GGAA | G | 6 | a0002 a0003 a0005 others(3): Show |
140 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
disruptive_inframe_deletion | MODERATE | c.908_910delAAG | p.Glu303del | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 11/12 | 1065/1441 | 908/1176 | 303/391 | INFO_REALIGN_3_PRIME | chr2 | 3701561 | ||
chr2:3702447 | C | G | 1 | a0002 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1060C>G | p.Pro354Ala | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 12/12 | 1217/1441 | 1060/1176 | 354/391 | chr2 | 3702447 | |||
chr2:3702471 | C | T | 1 | a0002 | 3 | HG02922.hp2 HG03453.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.1084C>T | p.Arg362Trp | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 12/12 | 1241/1441 | 1084/1176 | 362/391 | chr2 | 3702471 | |||
chr2:3702646 | ATTTAATA others(53): Show |
A | 1 | a0001 | 1 | HG00423.hp1 | splice_region_variant | LOW | c.*84_*143delTTTAATA others(53): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 12/12 | chr2 | 3702646 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:3678500 | T | C | 2 | a0002c0005 a0002c0009 |
7 | HG02647.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
synonymous_variant | LOW | c.117T>C | p.Tyr39Tyr | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/12 | 274/1441 | 117/1176 | 39/391 | chr2 | 3678500 | |||
chr2:3678503 | G | A | 1 | a0003c0010 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.120G>A | p.Thr40Thr | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/12 | 277/1441 | 120/1176 | 40/391 | chr2 | 3678503 | |||
chr2:3697386 | A | G | 1 | a0002c0015 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.780A>G | p.Glu260Glu | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/12 | 937/1441 | 780/1176 | 260/391 | chr2 | 3697386 | |||
chr2:3701543 | G | A | 1 | a0002c0009 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.882G>A | p.Gly294Gly | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 11/12 | 1039/1441 | 882/1176 | 294/391 | chr2 | 3701543 | |||
chr2:3702521 | G | A | 1 | a0002c0013 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.1134G>A | p.Lys378Lys | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 12/12 | 1291/1441 | 1134/1176 | 378/391 | chr2 | 3702521 | |||
chr2:3702539 | G | C | 1 | a0001c0012 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.1152G>C | p.Ser384Ser | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 12/12 | 1309/1441 | 1152/1176 | 384/391 | chr2 | 3702539 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:3658227 | C | T | 5 | a0001c0001t0003 a0003c0010t0004 a0004c0004t0003 others(2): Show |
9 | HG01123.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-130C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/12 | chr2 | 3658227 | |||||||
chr2:3658255 | C | G | 5 | a0001c0001t0003 a0003c0010t0004 a0004c0004t0003 others(2): Show |
9 | HG01123.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-102C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/12 | 12903 | chr2 | 3658255 | ||||||
chr2:3671102 | C | T | 15 | a0001c0001t0002 a0001c0012t0002 a0002c0002t0002 others(12): Show |
127 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-56C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/12 | chr2 | 3671102 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:3658392 | C | A | 6 | a0001c0001t0001g0025 a0002c0002t0002g0024 a0002c0005t0002g0022 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-63+98C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3658392 | |||||||
chr2:3658396 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-63+102C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3658396 | |||||||
chr2:3658397 | G | A | 23 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0040 others(20): Show |
25 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-63+103G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3658397 | |||||||
chr2:3658465 | C | T | 146 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(143): Show |
159 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.-63+171C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3658465 | |||||||
chr2:3658470 | C | T | 9 | a0001c0001t0003g0227 a0001c0001t0003g0230 a0003c0010t0004g0228 others(6): Show |
9 | HG01123.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-63+176C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3658470 | |||||||
chr2:3658484 | C | A | 1 | a0002c0005t0002g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-63+190C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3658484 | |||||||
chr2:3658568 | TA | T | 39 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0204 others(36): Show |
44 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-63+283delA | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3658568 | ||||||
chr2:3658694 | C | T | 9 | a0001c0001t0003g0227 a0001c0001t0003g0230 a0003c0010t0004g0228 others(6): Show |
9 | HG01123.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-63+400C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3658694 | |||||||
chr2:3658792 | C | T | 2 | a0003c0003t0002g0123 a0007c0011t0001g0124 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-63+498C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3658792 | |||||||
chr2:3658876 | C | CA | 20 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(17): Show |
20 | HG00735.hp2 HG01123.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.-63+601dupA | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3658876 | ||||||
chr2:3658876 | C | CAA | 31 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0204 others(28): Show |
36 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-63+600_-63+601dup others(2): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3658876 | ||||||
chr2:3658876 | C | CAAAA | 6 | a0001c0001t0003g0227 a0004c0004t0003g0223 a0004c0004t0003g0224 others(3): Show |
6 | HG01123.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-63+598_-63+601dup others(4): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3658876 | ||||||
chr2:3658876 | CA | C | 9 | a0001c0001t0002g0187 a0002c0002t0002g0186 a0002c0005t0002g0022 others(6): Show |
9 | HG01515.hp2 HG02486.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-63+601delA | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3658876 | ||||||
chr2:3658944 | G | A | 9 | a0001c0001t0003g0227 a0001c0001t0003g0230 a0003c0010t0004g0228 others(6): Show |
9 | HG01123.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-63+650G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3658944 | |||||||
chr2:3659032 | C | T | 30 | a0001c0001t0001g0166 a0001c0001t0001g0184 a0001c0001t0002g0187 others(27): Show |
34 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-63+738C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659032 | |||||||
chr2:3659222 | G | A | 41 | a0001c0001t0001g0166 a0001c0001t0001g0184 a0001c0001t0001g0232 others(38): Show |
45 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.-63+928G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659222 | |||||||
chr2:3659392 | C | T | 6 | a0001c0001t0003g0227 a0001c0001t0003g0230 a0005c0007t0004g0225 others(3): Show |
6 | HG01123.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-63+1098C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659392 | |||||||
chr2:3659430 | A | G | 41 | a0001c0001t0001g0166 a0001c0001t0001g0184 a0001c0001t0001g0232 others(38): Show |
45 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.-63+1136A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659430 | |||||||
chr2:3659496 | A | G | 9 | a0001c0001t0003g0227 a0001c0001t0003g0230 a0003c0010t0004g0228 others(6): Show |
9 | HG01123.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-63+1202A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659496 | |||||||
chr2:3659546 | T | C | 75 | a0001c0001t0001g0025 a0001c0001t0001g0166 a0001c0001t0001g0184 others(72): Show |
84 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.-63+1252T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659546 | |||||||
chr2:3659652 | A | G | 13 | a0002c0002t0001g0205 a0002c0002t0002g0209 a0002c0002t0002g0210 others(10): Show |
13 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-63+1358A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659652 | |||||||
chr2:3659663 | C | T | 9 | a0001c0001t0001g0114 a0001c0001t0001g0118 a0003c0003t0001g0005 others(6): Show |
11 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-63+1369C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659663 | |||||||
chr2:3659701 | G | C | 1 | a0003c0010t0004g0228 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-63+1407G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659701 | |||||||
chr2:3659719 | C | T | 9 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(6): Show |
9 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-63+1425C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659719 | |||||||
chr2:3659804 | C | T | 28 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0002g0127 others(25): Show |
30 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.-63+1510C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659804 | |||||||
chr2:3659833 | C | T | 106 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(103): Show |
115 | HG00544.hp1 HG00558.hp2 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.-63+1539C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659833 | |||||||
chr2:3659932 | G | T | 30 | a0001c0001t0001g0166 a0001c0001t0001g0184 a0001c0001t0002g0187 others(27): Show |
34 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-63+1638G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659932 | |||||||
chr2:3659992 | A | G | 3 | a0002c0005t0002g0022 a0003c0003t0002g0026 a0003c0003t0002g0027 |
3 | HG02896.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-63+1698A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3659992 | |||||||
chr2:3660056 | C | A | 43 | a0001c0001t0001g0025 a0001c0001t0001g0199 a0001c0001t0001g0203 others(40): Show |
48 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-63+1762C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3660056 | |||||||
chr2:3660185 | G | T | 37 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0143 others(34): Show |
39 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.-63+1891G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3660185 | |||||||
chr2:3660262 | T | C | 73 | a0001c0001t0001g0025 a0001c0001t0001g0166 a0001c0001t0001g0184 others(70): Show |
82 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-63+1968T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3660262 | |||||||
chr2:3660316 | T | C | 1 | a0001c0001t0002g0029 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-63+2022T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3660316 | |||||||
chr2:3660350 | T | C | 2 | a0001c0001t0002g0127 a0001c0001t0002g0138 |
2 | NA18995.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-63+2056T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3660350 | |||||||
chr2:3660659 | G | GC | 78 | a0001c0001t0001g0025 a0001c0001t0001g0166 a0001c0001t0001g0184 others(75): Show |
87 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-63+2369dupC | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3660659 | ||||||
chr2:3660721 | T | C | 79 | a0001c0001t0001g0025 a0001c0001t0001g0166 a0001c0001t0001g0184 others(76): Show |
88 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.-63+2427T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3660721 | |||||||
chr2:3660793 | A | T | 139 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(136): Show |
152 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.-63+2499A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3660793 | |||||||
chr2:3660819 | A | AATCGGAA others(21): Show |
9 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(6): Show |
9 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-63+2585_-63+2612d others(30): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3660819 | ||||||
chr2:3660819 | AATCGGAA others(21): Show |
A | 1 | a0002c0002t0002g0139 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-63+2585_-63+2612d others(30): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3660819 | ||||||
chr2:3660879 | G | GGAATGAG others(21): Show |
71 | a0001c0001t0001g0025 a0001c0001t0001g0166 a0001c0001t0001g0184 others(68): Show |
80 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-63+2612_-63+2613i others(30): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3660879 | ||||||
chr2:3660879 | G | GGATTGAG others(21): Show |
7 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0220 others(4): Show |
7 | HG00558.hp2 HG02071.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-63+2587_-63+2588i others(30): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3660879 | ||||||
chr2:3660913 | G | A | 78 | a0001c0001t0001g0025 a0001c0001t0001g0166 a0001c0001t0001g0184 others(75): Show |
87 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-63+2619G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3660913 | |||||||
chr2:3660997 | G | A | 1 | a0002c0002t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-63+2703G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3660997 | |||||||
chr2:3661095 | C | T | 72 | a0001c0001t0001g0166 a0001c0001t0001g0184 a0001c0001t0001g0199 others(69): Show |
81 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-63+2801C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661095 | |||||||
chr2:3661196 | T | G | 29 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0148 others(26): Show |
31 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.-63+2902T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661196 | |||||||
chr2:3661213 | C | G | 1 | a0002c0005t0002g0047 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-63+2919C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661213 | |||||||
chr2:3661270 | T | C | 1 | a0003c0003t0002g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-63+2976T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661270 | |||||||
chr2:3661292 | CAT | C | 72 | a0001c0001t0001g0166 a0001c0001t0001g0184 a0001c0001t0001g0199 others(69): Show |
81 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-63+2999_-63+3000d others(4): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661292 | |||||||
chr2:3661304 | A | T | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0003c0010t0004g0228 others(2): Show |
5 | HG01884.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-63+3010A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661304 | |||||||
chr2:3661376 | A | G | 148 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(145): Show |
161 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.-63+3082A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661376 | |||||||
chr2:3661518 | A | G | 139 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(136): Show |
152 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.-63+3224A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661518 | |||||||
chr2:3661539 | T | C | 72 | a0001c0001t0001g0166 a0001c0001t0001g0184 a0001c0001t0001g0199 others(69): Show |
81 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-63+3245T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661539 | |||||||
chr2:3661547 | C | G | 1 | a0002c0005t0001g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-63+3253C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661547 | |||||||
chr2:3661549 | G | C | 1 | a0002c0009t0002g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-63+3255G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661549 | |||||||
chr2:3661707 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-63+3413A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661707 | |||||||
chr2:3661743 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-63+3449C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661743 | |||||||
chr2:3661761 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-63+3467G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661761 | |||||||
chr2:3661785 | T | C | 29 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0148 others(26): Show |
31 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.-63+3491T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3661785 | |||||||
chr2:3662029 | CAA | C | 23 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0040 others(20): Show |
25 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-63+3736_-63+3737d others(4): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662029 | |||||||
chr2:3662032 | G | T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0040 others(20): Show |
25 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-63+3738G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662032 | |||||||
chr2:3662053 | A | T | 1 | a0001c0001t0001g0126 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-63+3759A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662053 | |||||||
chr2:3662171 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-63+3877G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662171 | |||||||
chr2:3662256 | C | T | 1 | a0002c0002t0002g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-63+3962C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662256 | |||||||
chr2:3662317 | A | G | 148 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(145): Show |
161 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.-63+4023A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662317 | |||||||
chr2:3662498 | G | A | 1 | a0003c0003t0002g0014 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-63+4204G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662498 | |||||||
chr2:3662525 | A | G | 3 | a0001c0001t0001g0025 a0002c0002t0002g0024 a0002c0009t0002g0023 |
3 | HG01884.hp1 HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-63+4231A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662525 | |||||||
chr2:3662538 | C | T | 16 | a0001c0001t0002g0020 a0001c0001t0002g0189 a0001c0001t0002g0190 others(13): Show |
21 | HG00544.hp1 HG00733.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.-63+4244C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662538 | |||||||
chr2:3662558 | A | G | 1 | a0002c0002t0002g0121 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-63+4264A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662558 | |||||||
chr2:3662579 | C | T | 16 | a0001c0001t0002g0020 a0001c0001t0002g0189 a0001c0001t0002g0190 others(13): Show |
21 | HG00544.hp1 HG00733.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.-63+4285C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662579 | |||||||
chr2:3662873 | G | A | 67 | a0001c0001t0001g0166 a0001c0001t0001g0184 a0001c0001t0001g0199 others(64): Show |
76 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.-63+4579G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662873 | |||||||
chr2:3662925 | C | T | 30 | a0001c0001t0001g0166 a0001c0001t0001g0184 a0001c0001t0002g0187 others(27): Show |
34 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-63+4631C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662925 | |||||||
chr2:3662957 | C | T | 1 | a0002c0002t0002g0197 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-63+4663C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662957 | |||||||
chr2:3662986 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-63+4692T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3662986 | |||||||
chr2:3663001 | G | A | 1 | a0002c0009t0002g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-63+4707G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3663001 | |||||||
chr2:3663216 | C | T | 31 | a0001c0001t0001g0025 a0001c0001t0001g0143 a0001c0001t0001g0148 others(28): Show |
33 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.-63+4922C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3663216 | |||||||
chr2:3663250 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0232 a0001c0001t0001g0233 others(2): Show |
5 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-63+4956G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3663250 | |||||||
chr2:3663348 | G | A | 98 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(95): Show |
109 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.-63+5054G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3663348 | |||||||
chr2:3663427 | G | A | 7 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0220 others(4): Show |
7 | HG00558.hp2 HG02071.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-63+5133G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3663427 | |||||||
chr2:3663535 | C | T | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-63+5241C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3663535 | |||||||
chr2:3663584 | G | GA | 29 | a0001c0001t0002g0020 a0001c0001t0002g0189 a0001c0001t0002g0190 others(26): Show |
34 | HG00544.hp1 HG00733.hp2 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.-63+5301dupA | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3663584 | ||||||
chr2:3663584 | GA | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0046 others(12): Show |
16 | HG00642.hp1 HG01106.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.-63+5301delA | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3663584 | ||||||
chr2:3663598 | C | G | 2 | a0004c0004t0003g0223 a0004c0004t0003g0224 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-63+5304C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3663598 | |||||||
chr2:3663631 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-63+5337A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3663631 | |||||||
chr2:3663881 | T | G | 3 | a0001c0001t0001g0025 a0002c0002t0002g0024 a0002c0009t0002g0023 |
3 | HG01884.hp1 HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-63+5587T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3663881 | |||||||
chr2:3663991 | C | T | 3 | a0002c0006t0001g0041 a0003c0003t0002g0042 a0003c0003t0002g0043 |
3 | HG02258.hp1 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-63+5697C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3663991 | |||||||
chr2:3664073 | G | A | 30 | a0001c0001t0001g0166 a0001c0001t0001g0184 a0001c0001t0002g0187 others(27): Show |
34 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-63+5779G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664073 | |||||||
chr2:3664329 | G | T | 98 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(95): Show |
109 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.-63+6035G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664329 | |||||||
chr2:3664348 | A | C | 1 | a0002c0002t0002g0217 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-63+6054A>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664348 | |||||||
chr2:3664349 | T | A | 1 | a0002c0002t0002g0217 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-63+6055T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664349 | |||||||
chr2:3664382 | A | G | 139 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(136): Show |
152 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.-63+6088A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664382 | |||||||
chr2:3664399 | A | G | 66 | a0001c0001t0001g0166 a0001c0001t0001g0184 a0001c0001t0001g0199 others(63): Show |
75 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.-63+6105A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664399 | |||||||
chr2:3664458 | T | G | 30 | a0001c0001t0001g0166 a0001c0001t0001g0184 a0001c0001t0002g0187 others(27): Show |
34 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-63+6164T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664458 | |||||||
chr2:3664472 | C | G | 16 | a0001c0001t0002g0020 a0001c0001t0002g0189 a0001c0001t0002g0190 others(13): Show |
21 | HG00544.hp1 HG00733.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.-63+6178C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664472 | |||||||
chr2:3664479 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-63+6185G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664479 | |||||||
chr2:3664502 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-63+6208G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664502 | |||||||
chr2:3664565 | G | A | 12 | a0002c0002t0001g0205 a0002c0002t0002g0209 a0002c0002t0002g0210 others(9): Show |
12 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-63+6271G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664565 | |||||||
chr2:3664693 | G | A | 31 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0148 others(28): Show |
33 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.-63+6399G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664693 | |||||||
chr2:3664751 | G | T | 1 | a0002c0002t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-62-6345G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664751 | |||||||
chr2:3664807 | C | T | 31 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0148 others(28): Show |
33 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.-62-6289C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664807 | |||||||
chr2:3664838 | C | A | 1 | a0004c0004t0001g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-62-6258C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664838 | |||||||
chr2:3664884 | C | CA | 15 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0232 others(12): Show |
15 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-62-6201dupA | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3664884 | ||||||
chr2:3664905 | A | AC | 4 | a0003c0010t0004g0228 a0004c0004t0001g0137 a0004c0004t0003g0223 others(1): Show |
4 | HG02258.hp2 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-62-6191_-62-6190i others(3): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664905 | |||||||
chr2:3664906 | A | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0040 others(30): Show |
35 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.-62-6190A>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664906 | |||||||
chr2:3664940 | ATTTCATT others(28): Show |
A | 1 | a0002c0002t0002g0217 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-62-6155_-62-6121d others(37): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3664940 | |||||||
chr2:3665139 | G | T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0040 others(20): Show |
25 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-62-5957G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3665139 | |||||||
chr2:3665272 | C | CT | 30 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0148 others(27): Show |
32 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-62-5815dupT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3665272 | ||||||
chr2:3665307 | T | G | 67 | a0001c0001t0001g0166 a0001c0001t0001g0184 a0001c0001t0001g0199 others(64): Show |
76 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.-62-5789T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3665307 | |||||||
chr2:3665311 | TTTTTAAA others(5): Show |
T | 1 | a0001c0001t0001g0111 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-62-5778_-62-5767d others(14): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3665311 | ||||||
chr2:3665316 | A | T | 4 | a0002c0009t0002g0023 a0002c0013t0002g0031 a0003c0003t0002g0006 others(1): Show |
5 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62-5780A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3665316 | |||||||
chr2:3665337 | G | A | 1 | a0002c0002t0002g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-62-5759G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3665337 | |||||||
chr2:3665512 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-62-5584G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3665512 | |||||||
chr2:3665582 | C | T | 1 | a0008c0016t0002g0160 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-62-5514C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3665582 | |||||||
chr2:3665590 | T | G | 37 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(34): Show |
39 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.-62-5506T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3665590 | |||||||
chr2:3665640 | A | C | 2 | a0002c0002t0002g0212 a0002c0002t0002g0213 |
2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-62-5456A>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3665640 | |||||||
chr2:3665653 | T | A | 3 | a0002c0005t0002g0022 a0003c0003t0002g0026 a0003c0003t0002g0027 |
3 | HG02896.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-62-5443T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3665653 | |||||||
chr2:3665810 | T | C | 11 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(8): Show |
11 | HG02486.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.-62-5286T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3665810 | |||||||
chr2:3665841 | G | A | 16 | a0001c0001t0002g0020 a0001c0001t0002g0189 a0001c0001t0002g0190 others(13): Show |
21 | HG00544.hp1 HG00733.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.-62-5255G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3665841 | |||||||
chr2:3665852 | T | C | 1 | a0002c0002t0002g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-62-5244T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3665852 | |||||||
chr2:3665932 | TG | T | 4 | a0002c0002t0001g0205 a0002c0005t0001g0207 a0002c0005t0001g0208 others(1): Show |
4 | HG02647.hp1 HG02818.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-62-5163delG | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3665932 | |||||||
chr2:3666068 | G | C | 16 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0189 others(13): Show |
21 | HG00544.hp1 HG00733.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.-62-5028G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666068 | |||||||
chr2:3666116 | G | C | 56 | a0001c0001t0001g0166 a0001c0001t0002g0020 a0001c0001t0002g0140 others(53): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-62-4980G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666116 | |||||||
chr2:3666165 | C | T | 1 | a0001c0001t0001g0013 | 2 | NA18944.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.-62-4931C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666165 | |||||||
chr2:3666216 | A | T | 133 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(130): Show |
146 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(143): Show |
intron_variant | MODIFIER | c.-62-4880A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666216 | |||||||
chr2:3666218 | T | G | 133 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(130): Show |
146 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(143): Show |
intron_variant | MODIFIER | c.-62-4878T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666218 | |||||||
chr2:3666308 | C | T | 1 | a0002c0002t0001g0109 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-62-4788C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666308 | |||||||
chr2:3666392 | C | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-62-4704C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666392 | |||||||
chr2:3666430 | G | A | 16 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0189 others(13): Show |
21 | HG00544.hp1 HG00733.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.-62-4666G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666430 | |||||||
chr2:3666461 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-62-4635T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666461 | |||||||
chr2:3666477 | C | A | 86 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(83): Show |
97 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.-62-4619C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666477 | |||||||
chr2:3666531 | C | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG02056.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-62-4565C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666531 | |||||||
chr2:3666539 | C | A | 79 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(76): Show |
90 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-62-4557C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666539 | |||||||
chr2:3666656 | C | T | 3 | a0002c0005t0001g0207 a0002c0005t0001g0208 a0002c0005t0001g0215 |
3 | HG02647.hp1 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-62-4440C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666656 | |||||||
chr2:3666660 | C | A | 1 | a0004c0004t0001g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-62-4436C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666660 | |||||||
chr2:3666671 | A | C | 28 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0189 others(25): Show |
33 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-62-4425A>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666671 | |||||||
chr2:3666675 | C | T | 10 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(7): Show |
10 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-62-4421C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666675 | |||||||
chr2:3666864 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-62-4232C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666864 | |||||||
chr2:3666968 | T | C | 1 | a0004c0004t0002g0110 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-62-4128T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3666968 | |||||||
chr2:3667075 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-62-4021T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667075 | |||||||
chr2:3667078 | G | A | 7 | a0002c0002t0002g0024 a0002c0002t0002g0162 a0002c0002t0002g0209 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-62-4018G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667078 | |||||||
chr2:3667243 | G | T | 1 | a0003c0003t0002g0193 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-62-3853G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667243 | |||||||
chr2:3667291 | C | T | 5 | a0001c0001t0001g0040 a0002c0002t0001g0205 a0002c0005t0001g0207 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-62-3805C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667291 | |||||||
chr2:3667374 | G | A | 4 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0146 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-62-3722G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667374 | |||||||
chr2:3667376 | T | G | 112 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0044 others(109): Show |
127 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-62-3720T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667376 | |||||||
chr2:3667377 | G | T | 112 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0044 others(109): Show |
127 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-62-3719G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667377 | |||||||
chr2:3667381 | A | G | 20 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0189 others(17): Show |
25 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-62-3715A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667381 | |||||||
chr2:3667382 | A | AT | 10 | a0001c0001t0001g0025 a0002c0013t0002g0031 a0003c0003t0002g0006 others(7): Show |
12 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-62-3713dupT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3667382 | ||||||
chr2:3667425 | C | T | 133 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(130): Show |
148 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.-62-3671C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667425 | |||||||
chr2:3667481 | G | A | 95 | a0001c0001t0001g0025 a0001c0001t0001g0166 a0001c0001t0001g0232 others(92): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-62-3615G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667481 | |||||||
chr2:3667494 | G | A | 7 | a0002c0002t0002g0212 a0002c0002t0002g0213 a0002c0005t0002g0022 others(4): Show |
7 | HG02647.hp2 HG02886.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-62-3602G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667494 | |||||||
chr2:3667561 | G | A | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0002c0002t0002g0212 others(6): Show |
9 | HG01346.hp2 HG02293.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-62-3535G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667561 | |||||||
chr2:3667707 | T | C | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0004c0004t0001g0137 |
3 | HG01884.hp2 HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-62-3389T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667707 | |||||||
chr2:3667737 | C | T | 27 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(24): Show |
30 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.-62-3359C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667737 | |||||||
chr2:3667833 | C | T | 19 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0006t0002g0135 others(16): Show |
21 | HG01123.hp2 HG01243.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.-62-3263C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667833 | |||||||
chr2:3667878 | C | T | 2 | a0004c0004t0003g0223 a0004c0004t0003g0224 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-62-3218C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667878 | |||||||
chr2:3667913 | C | T | 5 | a0001c0001t0001g0040 a0002c0002t0001g0205 a0002c0005t0001g0207 others(2): Show |
5 | HG02647.hp1 HG02818.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-62-3183C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3667913 | |||||||
chr2:3668089 | G | A | 1 | a0002c0005t0001g0206 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-62-3007G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668089 | |||||||
chr2:3668158 | G | A | 19 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0006t0002g0135 others(16): Show |
21 | HG01123.hp2 HG01243.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.-62-2938G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668158 | |||||||
chr2:3668200 | G | A | 1 | a0003c0003t0002g0183 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-62-2896G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668200 | |||||||
chr2:3668242 | G | A | 108 | a0001c0001t0001g0166 a0001c0001t0002g0020 a0001c0001t0002g0029 others(105): Show |
122 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-62-2854G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668242 | |||||||
chr2:3668400 | G | T | 7 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0220 others(4): Show |
7 | HG02071.hp1 HG02083.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.-62-2696G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668400 | |||||||
chr2:3668442 | C | T | 60 | a0001c0001t0002g0020 a0001c0001t0002g0029 a0001c0001t0002g0104 others(57): Show |
68 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.-62-2654C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668442 | |||||||
chr2:3668501 | C | T | 33 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(30): Show |
36 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.-62-2595C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668501 | |||||||
chr2:3668527 | T | C | 7 | a0002c0002t0002g0212 a0002c0002t0002g0213 a0002c0005t0002g0022 others(4): Show |
7 | HG02647.hp2 HG02886.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-62-2569T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668527 | |||||||
chr2:3668566 | C | CT | 11 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0001g0099 others(8): Show |
12 | HG01517.hp1 HG01934.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.-62-2503dupT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668566 | C | CTT | 5 | a0001c0001t0001g0132 a0001c0001t0001g0233 a0002c0006t0001g0041 others(2): Show |
5 | HG01884.hp2 HG03209.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-62-2504_-62-2503d others(4): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668566 | C | CTTT | 24 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(21): Show |
27 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.-62-2505_-62-2503d others(5): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668566 | C | CTTTT | 7 | a0001c0001t0002g0154 a0002c0002t0002g0061 a0002c0002t0002g0062 others(4): Show |
7 | HG00639.hp1 HG01081.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.-62-2506_-62-2503d others(6): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668566 | C | CTTTTT | 6 | a0002c0002t0002g0212 a0002c0002t0002g0213 a0002c0005t0002g0047 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-62-2507_-62-2503d others(7): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668566 | C | CTTTTTTT others(3): Show |
1 | a0002c0005t0002g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-62-2512_-62-2503d others(12): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668566 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-62-2514_-62-2503d others(14): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668566 | CT | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
30 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-62-2503delT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668566 | CTT | C | 15 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0220 others(12): Show |
15 | HG01123.hp2 HG01891.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-62-2504_-62-2503d others(4): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668566 | CTTT | C | 5 | a0002c0013t0002g0031 a0003c0003t0002g0006 a0003c0003t0002g0015 others(2): Show |
7 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-62-2505_-62-2503d others(5): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668566 | CTTTT | C | 8 | a0001c0001t0001g0046 a0001c0001t0003g0227 a0003c0003t0002g0030 others(5): Show |
8 | HG02109.hp2 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-62-2506_-62-2503d others(6): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668566 | CTTTTT | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0044 others(19): Show |
25 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.-62-2507_-62-2503d others(7): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668566 | CTTTTTT | C | 12 | a0002c0002t0002g0024 a0002c0002t0002g0162 a0002c0002t0002g0192 others(9): Show |
12 | HG01891.hp2 HG02056.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-62-2508_-62-2503d others(8): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668566 | CTTTTTTT | C | 45 | a0001c0001t0001g0166 a0001c0001t0002g0020 a0001c0001t0002g0140 others(42): Show |
54 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.-62-2509_-62-2503d others(9): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668566 | ||||||
chr2:3668622 | C | G | 24 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0044 others(21): Show |
27 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-62-2474C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668622 | |||||||
chr2:3668653 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0003g0227 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-62-2443G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668653 | |||||||
chr2:3668695 | C | T | 89 | a0001c0001t0001g0166 a0001c0001t0002g0020 a0001c0001t0002g0029 others(86): Show |
101 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-62-2401C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668695 | |||||||
chr2:3668791 | G | A | 28 | a0001c0001t0001g0166 a0001c0001t0002g0187 a0002c0002t0002g0019 others(25): Show |
32 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.-62-2305G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668791 | |||||||
chr2:3668795 | C | T | 1 | a0003c0003t0002g0159 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-62-2301C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668795 | |||||||
chr2:3668796 | G | A | 89 | a0001c0001t0001g0166 a0001c0001t0002g0020 a0001c0001t0002g0029 others(86): Show |
101 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-62-2300G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668796 | |||||||
chr2:3668866 | G | A | 87 | a0001c0001t0001g0166 a0001c0001t0002g0020 a0001c0001t0002g0029 others(84): Show |
99 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-62-2230G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668866 | |||||||
chr2:3668889 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-62-2207T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3668889 | |||||||
chr2:3668976 | TCACCAGC others(7): Show |
T | 1 | a0004c0004t0002g0180 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-62-2117_-62-2104d others(16): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3668976 | ||||||
chr2:3669190 | C | A | 115 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0203 others(112): Show |
129 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.-62-1906C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669190 | |||||||
chr2:3669211 | C | T | 1 | a0003c0003t0002g0122 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-62-1885C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669211 | |||||||
chr2:3669239 | C | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0220 others(3): Show |
6 | HG02071.hp1 HG02083.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.-62-1857C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669239 | |||||||
chr2:3669309 | T | A | 36 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0203 others(33): Show |
40 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-62-1787T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669309 | |||||||
chr2:3669366 | C | T | 14 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0002c0002t0001g0205 others(11): Show |
14 | HG01884.hp1 HG02647.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.-62-1730C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669366 | |||||||
chr2:3669408 | C | T | 90 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0203 others(87): Show |
99 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.-62-1688C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669408 | |||||||
chr2:3669432 | C | A | 1 | a0002c0002t0002g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-62-1664C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669432 | |||||||
chr2:3669433 | C | T | 2 | a0001c0001t0001g0025 a0006c0008t0003g0231 |
2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-62-1663C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669433 | |||||||
chr2:3669504 | C | T | 36 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0203 others(33): Show |
40 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-62-1592C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669504 | |||||||
chr2:3669646 | T | G | 1 | a0003c0003t0002g0016 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-62-1450T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669646 | |||||||
chr2:3669683 | C | T | 1 | a0002c0006t0001g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-62-1413C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669683 | |||||||
chr2:3669786 | G | A | 4 | a0003c0003t0002g0030 a0003c0003t0002g0039 a0003c0003t0002g0048 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-62-1310G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669786 | |||||||
chr2:3669792 | C | T | 5 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0146 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-62-1304C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669792 | |||||||
chr2:3669797 | C | T | 20 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0189 others(17): Show |
25 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-62-1299C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669797 | |||||||
chr2:3669798 | G | A | 7 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0220 others(4): Show |
7 | HG02071.hp1 HG02083.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.-62-1298G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669798 | |||||||
chr2:3669859 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-62-1237C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669859 | |||||||
chr2:3669906 | T | G | 154 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(151): Show |
171 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.-62-1190T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669906 | |||||||
chr2:3669924 | C | T | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.-62-1172C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669924 | |||||||
chr2:3669933 | G | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG01071.hp2 HG01952.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-62-1163G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669933 | |||||||
chr2:3669977 | A | C | 113 | a0001c0001t0001g0166 a0001c0001t0002g0020 a0001c0001t0002g0029 others(110): Show |
127 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-62-1119A>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3669977 | |||||||
chr2:3670077 | C | T | 32 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0144 others(29): Show |
37 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.-62-1019C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670077 | |||||||
chr2:3670083 | C | T | 32 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0144 others(29): Show |
37 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.-62-1013C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670083 | |||||||
chr2:3670235 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-62-861T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670235 | |||||||
chr2:3670260 | A | G | 3 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-62-836A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670260 | |||||||
chr2:3670355 | G | A | 7 | a0002c0002t0002g0212 a0002c0002t0002g0213 a0002c0005t0002g0022 others(4): Show |
7 | HG02647.hp2 HG02886.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-62-741G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670355 | |||||||
chr2:3670374 | C | T | 1 | a0003c0003t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-62-722C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670374 | |||||||
chr2:3670395 | C | T | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.-62-701C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670395 | |||||||
chr2:3670440 | G | A | 2 | a0004c0004t0003g0223 a0004c0004t0003g0224 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-62-656G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670440 | |||||||
chr2:3670615 | C | T | 1 | a0003c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-62-481C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670615 | |||||||
chr2:3670637 | T | C | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.-62-459T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670637 | |||||||
chr2:3670783 | C | T | 47 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(44): Show |
52 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.-62-313C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670783 | |||||||
chr2:3670803 | A | C | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.-62-293A>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670803 | |||||||
chr2:3670832 | G | T | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.-62-264G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670832 | |||||||
chr2:3670863 | T | A | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.-62-233T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670863 | |||||||
chr2:3670865 | T | TAGAAGGG others(310): Show |
3 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-62-225_-62-224ins others(317): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3670865 | ||||||
chr2:3670865 | T | TAGAAGGG others(309): Show |
4 | a0003c0003t0002g0030 a0003c0003t0002g0039 a0003c0003t0002g0048 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-62-225_-62-224ins others(316): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3670865 | ||||||
chr2:3670865 | T | TAGAAGGG others(309): Show |
1 | a0003c0003t0002g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-62-225_-62-224ins others(316): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3670865 | ||||||
chr2:3670865 | T | TAGAAGGG others(310): Show |
9 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0002t0002g0212 others(6): Show |
9 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-62-225_-62-224ins others(317): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3670865 | ||||||
chr2:3670865 | T | TAGAAGGG others(311): Show |
2 | a0003c0003t0002g0026 a0003c0003t0002g0027 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-62-225_-62-224ins others(318): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3670865 | ||||||
chr2:3670865 | T | TAGAAGGG others(308): Show |
4 | a0001c0001t0002g0127 a0002c0002t0002g0062 a0002c0002t0002g0186 others(1): Show |
4 | HG01081.hp1 HG01515.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-62-225_-62-224ins others(315): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3670865 | ||||||
chr2:3670865 | T | TAGAAGGG others(309): Show |
28 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0138 others(25): Show |
33 | HG00639.hp1 HG01081.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.-62-225_-62-224ins others(316): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3670865 | ||||||
chr2:3670865 | T | TAGAAGGG others(310): Show |
1 | a0003c0010t0004g0228 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-62-225_-62-224ins others(317): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3670865 | ||||||
chr2:3670865 | T | TAGAAGGG others(309): Show |
1 | a0002c0002t0002g0121 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-62-225_-62-224ins others(316): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3670865 | ||||||
chr2:3670865 | T | TAGAAGGG others(309): Show |
1 | a0006c0008t0002g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-62-225_-62-224ins others(316): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3670865 | ||||||
chr2:3670903 | C | T | 1 | a0002c0006t0001g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-62-193C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670903 | |||||||
chr2:3670918 | T | C | 3 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-62-178T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670918 | |||||||
chr2:3670921 | C | CT | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.-62-170dupT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 3670921 | ||||||
chr2:3670959 | A | G | 1 | a0003c0003t0001g0098 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-62-137A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670959 | |||||||
chr2:3670972 | A | G | 1 | a0004c0004t0001g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-62-124A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3670972 | |||||||
chr2:3671056 | G | A | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.-62-40G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3671056 | |||||||
chr2:3671065 | A | G | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.-62-31A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 1/11 | chr2 | 3671065 | |||||||
chr2:3671279 | C | A | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.33+89C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671279 | |||||||
chr2:3671395 | A | G | 114 | a0001c0001t0001g0166 a0001c0001t0002g0020 a0001c0001t0002g0029 others(111): Show |
128 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.33+205A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671395 | |||||||
chr2:3671525 | AGGAGGTC others(201): Show |
A | 1 | a0002c0009t0002g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.33+361_33+568del | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 3671525 | ||||||
chr2:3671551 | A | G | 53 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(50): Show |
58 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.33+361A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671551 | |||||||
chr2:3671554 | AGGTCCTC others(149): Show |
A | 53 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(50): Show |
58 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.33+405_33+560del | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 3671554 | ||||||
chr2:3671710 | TGGTCCTC others(149): Show |
T | 1 | a0002c0002t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.33+569_33+724del | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 3671710 | ||||||
chr2:3671747 | C | T | 53 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(50): Show |
58 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.33+557C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671747 | |||||||
chr2:3671759 | C | G | 55 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(52): Show |
60 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.33+569C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671759 | |||||||
chr2:3671768 | T | C | 53 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(50): Show |
58 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.33+578T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671768 | |||||||
chr2:3671799 | C | T | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.33+609C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671799 | |||||||
chr2:3671837 | T | C | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.33+647T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671837 | |||||||
chr2:3671837 | T | G | 30 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(27): Show |
33 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.33+647T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671837 | |||||||
chr2:3671841 | G | A | 28 | a0001c0001t0001g0166 a0001c0001t0002g0187 a0002c0002t0002g0019 others(25): Show |
32 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.33+651G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671841 | |||||||
chr2:3671855 | G | A | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.33+665G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671855 | |||||||
chr2:3671872 | T | C | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.33+682T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671872 | |||||||
chr2:3671883 | T | G | 32 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0144 others(29): Show |
37 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.33+693T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671883 | |||||||
chr2:3671916 | GGAGGTCC others(45): Show |
G | 1 | a0001c0001t0001g0166 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.33+770_33+821delTT others(50): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 3671916 | ||||||
chr2:3671924 | T | C | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.33+734T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671924 | |||||||
chr2:3671933 | A | G | 2 | a0004c0004t0003g0223 a0004c0004t0003g0224 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.33+743A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671933 | |||||||
chr2:3671934 | T | G | 2 | a0004c0004t0003g0223 a0004c0004t0003g0224 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.33+744T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671934 | |||||||
chr2:3671934 | TTTAGATC others(71): Show |
T | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.33+770_33+847delTT others(76): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 3671934 | ||||||
chr2:3671941 | C | G | 2 | a0004c0004t0003g0223 a0004c0004t0003g0224 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.33+751C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671941 | |||||||
chr2:3671942 | C | G | 2 | a0004c0004t0003g0223 a0004c0004t0003g0224 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.33+752C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671942 | |||||||
chr2:3671960 | TTTAGATC others(45): Show |
T | 11 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0146 others(8): Show |
11 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.33+796_33+847delTT others(50): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 3671960 | ||||||
chr2:3671968 | CGAGGTCC others(383): Show |
C | 27 | a0001c0001t0002g0187 a0002c0002t0002g0019 a0002c0002t0002g0175 others(24): Show |
31 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.33+828_33+1217del | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 3671968 | ||||||
chr2:3671985 | ATTTAGAT others(617): Show |
A | 36 | a0001c0001t0002g0104 a0001c0001t0002g0127 a0002c0002t0002g0004 others(33): Show |
36 | HG00639.hp1 HG01081.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.33+796_33+1419del | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671985 | |||||||
chr2:3671985 | ATTTAGAT others(643): Show |
A | 22 | a0001c0001t0002g0029 a0001c0001t0002g0138 a0001c0001t0002g0154 others(19): Show |
23 | HG01081.hp2 HG01243.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.33+796_34-1440del | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3671985 | |||||||
chr2:3671986 | TTTAGATC others(19): Show |
T | 27 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0220 others(24): Show |
32 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.33+828_33+853delTC others(24): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 3671986 | ||||||
chr2:3672018 | T | C | 1 | a0004c0004t0001g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.33+828T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672018 | |||||||
chr2:3672020 | C | T | 1 | a0004c0004t0001g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.33+830C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672020 | |||||||
chr2:3672022 | A | T | 1 | a0004c0004t0001g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.33+832A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672022 | |||||||
chr2:3672035 | CTAGTTAG others(45): Show |
C | 1 | a0004c0004t0001g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.33+847_33+898delAG others(50): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 3672035 | ||||||
chr2:3672087 | G | C | 72 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(69): Show |
80 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.33+897G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672087 | |||||||
chr2:3672097 | C | G | 1 | a0004c0004t0001g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.33+907C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672097 | |||||||
chr2:3672115 | A | G | 1 | a0004c0004t0001g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.33+925A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672115 | |||||||
chr2:3672123 | T | G | 20 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0189 others(17): Show |
25 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.33+933T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672123 | |||||||
chr2:3672163 | G | T | 2 | a0004c0004t0003g0223 a0004c0004t0003g0224 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.33+973G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672163 | |||||||
chr2:3672194 | A | G | 20 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0189 others(17): Show |
25 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.33+1004A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672194 | |||||||
chr2:3672306 | G | A | 31 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(28): Show |
34 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.33+1116G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672306 | |||||||
chr2:3672309 | A | G | 20 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0189 others(17): Show |
25 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.33+1119A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672309 | |||||||
chr2:3672331 | A | G | 20 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0189 others(17): Show |
25 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.33+1141A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672331 | |||||||
chr2:3672375 | A | G | 32 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0144 others(29): Show |
37 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.33+1185A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672375 | |||||||
chr2:3672399 | C | T | 1 | a0002c0002t0002g0188 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.33+1209C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672399 | |||||||
chr2:3672461 | C | G | 27 | a0001c0001t0002g0187 a0002c0002t0002g0019 a0002c0002t0002g0175 others(24): Show |
31 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.33+1271C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672461 | |||||||
chr2:3672488 | G | A | 1 | a0001c0001t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.33+1298G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672488 | |||||||
chr2:3672539 | AGGAGGTC others(45): Show |
A | 59 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0144 others(56): Show |
68 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.33+1375_33+1426del others(52): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 3672539 | ||||||
chr2:3672616 | T | C | 36 | a0001c0001t0002g0104 a0001c0001t0002g0127 a0002c0002t0002g0004 others(33): Show |
36 | HG00639.hp1 HG01081.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.33+1426T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672616 | |||||||
chr2:3672617 | AGGAGGTC others(19): Show |
C | 36 | a0001c0001t0002g0104 a0001c0001t0002g0127 a0002c0002t0002g0004 others(33): Show |
36 | HG00639.hp1 HG01081.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.33+1427_34-1432del others(31): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672617 | |||||||
chr2:3672642 | T | C | 22 | a0001c0001t0002g0029 a0001c0001t0002g0138 a0001c0001t0002g0154 others(19): Show |
23 | HG01081.hp2 HG01243.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.34-1433T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672642 | |||||||
chr2:3672643 | G | C | 22 | a0001c0001t0002g0029 a0001c0001t0002g0138 a0001c0001t0002g0154 others(19): Show |
23 | HG01081.hp2 HG01243.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.34-1432G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672643 | |||||||
chr2:3672644 | G | T | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.34-1431G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672644 | |||||||
chr2:3672646 | A | T | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.34-1429A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672646 | |||||||
chr2:3672663 | T | C | 1 | a0001c0001t0002g0144 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.34-1412T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672663 | |||||||
chr2:3672673 | GGTCCTCT others(45): Show |
G | 2 | a0004c0004t0003g0223 a0004c0004t0003g0224 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.34-1380_34-1329del others(52): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 3672673 | ||||||
chr2:3672747 | A | G | 1 | a0002c0002t0002g0185 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.34-1328A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672747 | |||||||
chr2:3672798 | C | T | 2 | a0004c0004t0003g0223 a0004c0004t0003g0224 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.34-1277C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672798 | |||||||
chr2:3672830 | G | A | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.34-1245G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672830 | |||||||
chr2:3672916 | G | A | 27 | a0001c0001t0002g0187 a0002c0002t0002g0019 a0002c0002t0002g0175 others(24): Show |
31 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.34-1159G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3672916 | |||||||
chr2:3673012 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG02056.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.34-1063G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3673012 | |||||||
chr2:3673074 | T | C | 113 | a0001c0001t0002g0020 a0001c0001t0002g0029 a0001c0001t0002g0104 others(110): Show |
127 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.34-1001T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3673074 | |||||||
chr2:3673117 | C | G | 47 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(44): Show |
52 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.34-958C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3673117 | |||||||
chr2:3673222 | C | A | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.34-853C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3673222 | |||||||
chr2:3673246 | C | A | 32 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0144 others(29): Show |
37 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.34-829C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3673246 | |||||||
chr2:3673310 | G | A | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.34-765G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3673310 | |||||||
chr2:3673537 | A | G | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.34-538A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3673537 | |||||||
chr2:3673606 | T | C | 5 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0146 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.34-469T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3673606 | |||||||
chr2:3673713 | C | T | 1 | a0003c0003t0002g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.34-362C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3673713 | |||||||
chr2:3673763 | G | C | 49 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(46): Show |
54 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.34-312G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3673763 | |||||||
chr2:3674010 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0078 |
2 | HG00735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.34-65G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3674010 | |||||||
chr2:3674042 | G | A | 108 | a0001c0001t0002g0020 a0001c0001t0002g0029 a0001c0001t0002g0104 others(105): Show |
122 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.34-33G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | chr2 | 3674042 | |||||||
chr2:3674047 | ATCTT | A | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
splice_region_variant&intron_variant | LOW | c.34-10_34-7delCTTT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 3674047 | ||||||
chr2:3674139 | A | G | 163 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(160): Show |
180 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.84+14A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3674139 | |||||||
chr2:3674231 | A | G | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.84+106A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3674231 | |||||||
chr2:3674271 | C | A | 1 | a0003c0003t0002g0168 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.84+146C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3674271 | |||||||
chr2:3674346 | C | A | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.84+221C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3674346 | |||||||
chr2:3674378 | T | A | 4 | a0003c0003t0002g0016 a0003c0003t0002g0017 a0003c0003t0002g0136 others(1): Show |
6 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+253T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3674378 | |||||||
chr2:3674514 | C | A | 33 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0144 others(30): Show |
38 | HG00280.hp1 HG00544.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.84+389C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3674514 | |||||||
chr2:3674550 | C | T | 31 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(28): Show |
34 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.84+425C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3674550 | |||||||
chr2:3674660 | T | C | 54 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(51): Show |
59 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.84+535T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3674660 | |||||||
chr2:3674673 | C | T | 1 | a0002c0002t0002g0024 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.84+548C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3674673 | |||||||
chr2:3674744 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0046 others(1): Show |
5 | HG01106.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+619A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3674744 | |||||||
chr2:3674904 | A | G | 59 | a0001c0001t0002g0020 a0001c0001t0002g0140 a0001c0001t0002g0144 others(56): Show |
68 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.84+779A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3674904 | |||||||
chr2:3674989 | A | G | 56 | a0001c0001t0002g0029 a0001c0001t0002g0104 a0001c0001t0002g0127 others(53): Show |
61 | HG00639.hp1 HG01081.hp1 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.84+864A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3674989 | |||||||
chr2:3675037 | T | A | 6 | a0001c0001t0001g0203 a0001c0001t0001g0220 a0002c0002t0001g0202 others(3): Show |
6 | HG02071.hp1 HG02083.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+912T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3675037 | |||||||
chr2:3675387 | C | CAA | 6 | a0002c0002t0002g0212 a0002c0002t0002g0213 a0002c0005t0002g0022 others(3): Show |
6 | HG02647.hp2 HG02886.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+1279_84+1280dup others(2): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 3675387 | ||||||
chr2:3675387 | CA | C | 16 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(13): Show |
16 | HG00544.hp2 HG01081.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.84+1280delA | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 3675387 | ||||||
chr2:3675387 | CAA | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(146): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.84+1279_84+1280del others(2): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 3675387 | ||||||
chr2:3675436 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(139): Show |
174 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.84+1311G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3675436 | |||||||
chr2:3675583 | C | CAT | 24 | a0001c0001t0002g0190 a0001c0012t0002g0216 a0002c0002t0002g0003 others(21): Show |
28 | HG00280.hp1 HG00733.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.84+1474_84+1475dup others(2): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 3675583 | ||||||
chr2:3675595 | T | TAC | 3 | a0002c0005t0002g0022 a0002c0005t0002g0047 a0002c0009t0002g0023 |
3 | HG02886.hp1 HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.84+1471_84+1472ins others(2): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 3675595 | ||||||
chr2:3675597 | T | C | 5 | a0001c0001t0001g0025 a0002c0005t0002g0022 a0002c0005t0002g0047 others(2): Show |
5 | HG01884.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+1472T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3675597 | |||||||
chr2:3675597 | TATAC | T | 7 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0006t0002g0135 others(4): Show |
7 | HG01123.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+1474_84+1477del others(4): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 3675597 | ||||||
chr2:3675599 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(159): Show |
191 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.84+1474T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3675599 | |||||||
chr2:3675599 | T | TAC | 3 | a0003c0003t0002g0017 a0003c0003t0002g0136 a0003c0003t0002g0163 |
4 | HG00735.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+1486_84+1487dup others(2): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 3675599 | ||||||
chr2:3675613 | T | C | 14 | a0001c0001t0002g0144 a0002c0005t0001g0206 a0003c0003t0001g0038 others(11): Show |
14 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.84+1488T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3675613 | |||||||
chr2:3675728 | C | T | 1 | a0002c0002t0002g0155 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.84+1603C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3675728 | |||||||
chr2:3675729 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.84+1604G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3675729 | |||||||
chr2:3675817 | G | A | 1 | a0002c0005t0002g0047 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.84+1692G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3675817 | |||||||
chr2:3675826 | G | A | 5 | a0002c0002t0002g0133 a0002c0005t0002g0022 a0002c0005t0002g0047 others(2): Show |
5 | HG02809.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+1701G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3675826 | |||||||
chr2:3675874 | G | A | 21 | a0003c0003t0002g0016 a0003c0003t0002g0017 a0003c0003t0002g0018 others(18): Show |
24 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.84+1749G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3675874 | |||||||
chr2:3675962 | C | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(161): Show |
200 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.84+1837C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3675962 | |||||||
chr2:3675967 | T | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(191): Show |
232 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.84+1842T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3675967 | |||||||
chr2:3675993 | G | A | 1 | a0002c0002t0002g0103 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.84+1868G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3675993 | |||||||
chr2:3676020 | A | G | 10 | a0002c0005t0001g0206 a0002c0005t0002g0022 a0002c0005t0002g0047 others(7): Show |
10 | HG02451.hp1 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+1895A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3676020 | |||||||
chr2:3676054 | C | T | 3 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0014t0002g0218 |
3 | HG02809.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.84+1929C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3676054 | |||||||
chr2:3676090 | G | A | 1 | a0002c0002t0002g0222 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.84+1965G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3676090 | |||||||
chr2:3676280 | T | C | 2 | a0001c0001t0002g0127 a0001c0001t0002g0138 |
2 | NA18995.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.84+2155T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3676280 | |||||||
chr2:3676284 | T | C | 17 | a0002c0005t0001g0206 a0002c0005t0001g0207 a0002c0005t0001g0208 others(14): Show |
17 | HG01123.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.84+2159T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3676284 | |||||||
chr2:3676344 | A | G | 9 | a0003c0003t0002g0030 a0003c0003t0002g0039 a0003c0003t0002g0048 others(6): Show |
9 | HG01123.hp2 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-2124A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3676344 | |||||||
chr2:3676430 | C | T | 1 | a0002c0013t0002g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.85-2038C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3676430 | |||||||
chr2:3676478 | C | A | 21 | a0001c0001t0002g0190 a0002c0002t0001g0070 a0002c0002t0001g0109 others(18): Show |
25 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.85-1990C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3676478 | |||||||
chr2:3676746 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.85-1722G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3676746 | |||||||
chr2:3676766 | G | A | 1 | a0003c0003t0002g0163 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.85-1702G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3676766 | |||||||
chr2:3676780 | T | TTC | 44 | a0001c0001t0001g0040 a0001c0001t0001g0125 a0001c0001t0001g0126 others(41): Show |
47 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.85-1672_85-1671dup others(2): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 3676780 | ||||||
chr2:3676796 | C | CT | 17 | a0001c0001t0002g0190 a0002c0002t0001g0070 a0002c0002t0001g0109 others(14): Show |
21 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.85-1663dupT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 3676796 | ||||||
chr2:3676975 | A | AG | 8 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0044 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-1488dupG | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 3676975 | ||||||
chr2:3677030 | C | T | 2 | a0003c0003t0002g0026 a0003c0003t0002g0027 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.85-1438C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3677030 | |||||||
chr2:3677077 | C | T | 42 | a0003c0003t0001g0053 a0003c0003t0001g0065 a0003c0003t0001g0097 others(39): Show |
45 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.85-1391C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3677077 | |||||||
chr2:3677352 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85-1116C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3677352 | |||||||
chr2:3677531 | A | G | 82 | a0001c0001t0001g0040 a0001c0001t0001g0125 a0001c0001t0001g0126 others(79): Show |
90 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.85-937A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3677531 | |||||||
chr2:3677577 | A | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0094 a0001c0001t0001g0113 |
3 | HG00642.hp2 HG01192.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.85-891A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3677577 | |||||||
chr2:3677605 | G | A | 2 | a0003c0003t0002g0221 a0007c0011t0001g0124 |
2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.85-863G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3677605 | |||||||
chr2:3677629 | G | T | 5 | a0002c0002t0002g0024 a0003c0003t0002g0028 a0003c0003t0002g0123 others(2): Show |
5 | HG02055.hp1 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-839G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3677629 | |||||||
chr2:3677679 | C | T | 26 | a0001c0001t0001g0040 a0001c0001t0001g0125 a0001c0001t0001g0126 others(23): Show |
29 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.85-789C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3677679 | |||||||
chr2:3677784 | T | G | 47 | a0001c0001t0002g0190 a0002c0002t0001g0069 a0002c0002t0001g0070 others(44): Show |
54 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.85-684T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3677784 | |||||||
chr2:3677815 | A | T | 1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.85-653A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3677815 | |||||||
chr2:3677847 | C | T | 9 | a0003c0003t0001g0038 a0004c0004t0001g0035 a0004c0004t0001g0036 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-621C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3677847 | |||||||
chr2:3677908 | A | C | 1 | a0002c0002t0001g0086 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.85-560A>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3677908 | |||||||
chr2:3677996 | A | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0002g0187 |
3 | NA18965.hp1 NA19057.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.85-472A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3677996 | |||||||
chr2:3678050 | C | T | 1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.85-418C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3678050 | |||||||
chr2:3678171 | G | A | 8 | a0003c0003t0001g0052 a0003c0003t0001g0115 a0003c0003t0001g0116 others(5): Show |
9 | HG00642.hp1 HG00741.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-297G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3678171 | |||||||
chr2:3678374 | C | T | 47 | a0001c0001t0002g0190 a0002c0002t0001g0069 a0002c0002t0001g0070 others(44): Show |
54 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.85-94C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3678374 | |||||||
chr2:3678392 | G | A | 1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.85-76G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3678392 | |||||||
chr2:3678462 | C | A | 7 | a0002c0005t0001g0206 a0002c0005t0001g0207 a0002c0005t0001g0208 others(4): Show |
7 | HG02647.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.85-6C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 3/11 | chr2 | 3678462 | |||||||
chr2:3678572 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0184 |
3 | NA18979.hp2 NA18999.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.172+17G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3678572 | |||||||
chr2:3678573 | T | C | 143 | a0001c0001t0001g0040 a0001c0001t0001g0074 a0001c0001t0001g0125 others(140): Show |
158 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.172+18T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3678573 | |||||||
chr2:3678654 | A | G | 14 | a0003c0003t0002g0006 a0003c0003t0002g0015 a0003c0003t0002g0030 others(11): Show |
16 | HG01123.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.172+99A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3678654 | |||||||
chr2:3678722 | G | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG03486.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.172+167G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3678722 | |||||||
chr2:3678728 | G | A | 5 | a0003c0003t0002g0006 a0003c0003t0002g0015 a0003c0003t0002g0032 others(2): Show |
7 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+173G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3678728 | |||||||
chr2:3678783 | G | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0044 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.172+228G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3678783 | |||||||
chr2:3678785 | G | A | 2 | a0002c0002t0002g0149 a0002c0002t0002g0155 |
2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.172+230G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3678785 | |||||||
chr2:3678811 | C | G | 3 | a0002c0002t0002g0162 a0002c0002t0002g0210 a0002c0002t0002g0214 |
3 | HG02145.hp2 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.172+256C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3678811 | |||||||
chr2:3678933 | A | G | 1 | a0002c0002t0002g0152 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.172+378A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3678933 | |||||||
chr2:3679019 | G | A | 5 | a0002c0002t0002g0024 a0003c0003t0002g0028 a0003c0003t0002g0123 others(2): Show |
5 | HG02055.hp1 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+464G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3679019 | |||||||
chr2:3679051 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.172+496C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3679051 | |||||||
chr2:3679083 | C | T | 1 | a0002c0002t0002g0191 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.172+528C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3679083 | |||||||
chr2:3679232 | A | G | 14 | a0003c0003t0002g0006 a0003c0003t0002g0015 a0003c0003t0002g0030 others(11): Show |
16 | HG01123.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.173-637A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3679232 | |||||||
chr2:3679266 | A | G | 14 | a0003c0003t0002g0006 a0003c0003t0002g0015 a0003c0003t0002g0030 others(11): Show |
16 | HG01123.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.173-603A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3679266 | |||||||
chr2:3679318 | G | T | 3 | a0003c0003t0002g0028 a0006c0008t0002g0181 a0006c0008t0003g0231 |
3 | HG02055.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.173-551G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3679318 | |||||||
chr2:3679410 | A | G | 30 | a0002c0002t0001g0069 a0002c0002t0001g0071 a0002c0002t0001g0080 others(27): Show |
33 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.173-459A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3679410 | |||||||
chr2:3679413 | G | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG03195.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-456G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3679413 | |||||||
chr2:3679558 | A | G | 1 | a0003c0003t0001g0201 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.173-311A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3679558 | |||||||
chr2:3679588 | T | C | 2 | a0002c0002t0002g0149 a0002c0002t0002g0155 |
2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.173-281T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3679588 | |||||||
chr2:3679626 | C | G | 15 | a0003c0003t0002g0006 a0003c0003t0002g0015 a0003c0003t0002g0028 others(12): Show |
17 | HG01123.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.173-243C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3679626 | |||||||
chr2:3679678 | G | C | 7 | a0003c0003t0002g0028 a0003c0003t0002g0030 a0003c0003t0002g0039 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.173-191G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3679678 | |||||||
chr2:3679707 | A | C | 17 | a0001c0001t0002g0190 a0002c0002t0001g0070 a0002c0002t0001g0109 others(14): Show |
21 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.173-162A>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 4/11 | chr2 | 3679707 | |||||||
chr2:3680040 | T | G | 7 | a0003c0003t0002g0028 a0003c0003t0002g0030 a0003c0003t0002g0039 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+46T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3680040 | |||||||
chr2:3680133 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0101 |
2 | NA18943.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.298+139G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3680133 | |||||||
chr2:3680211 | T | C | 5 | a0001c0001t0001g0040 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG03195.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+217T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3680211 | |||||||
chr2:3680273 | G | A | 12 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0014t0002g0218 others(9): Show |
12 | HG02257.hp1 HG02258.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.298+279G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3680273 | |||||||
chr2:3680328 | C | T | 3 | a0003c0003t0002g0042 a0003c0003t0002g0043 a0003c0003t0002g0122 |
3 | HG02258.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.298+334C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3680328 | |||||||
chr2:3680403 | T | TGTGATGG others(57): Show |
1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.298+418_298+419ins others(64): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 3680403 | ||||||
chr2:3680514 | G | A | 10 | a0003c0003t0002g0028 a0003c0003t0002g0030 a0003c0003t0002g0039 others(7): Show |
10 | HG01123.hp2 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.298+520G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3680514 | |||||||
chr2:3680620 | C | G | 1 | a0002c0002t0002g0128 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.298+626C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3680620 | |||||||
chr2:3680687 | A | G | 26 | a0003c0003t0001g0005 a0003c0003t0001g0052 a0003c0003t0001g0115 others(23): Show |
31 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.298+693A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3680687 | |||||||
chr2:3680715 | T | C | 26 | a0003c0003t0001g0005 a0003c0003t0001g0052 a0003c0003t0001g0115 others(23): Show |
31 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.298+721T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3680715 | |||||||
chr2:3680764 | G | T | 7 | a0002c0005t0001g0206 a0002c0005t0001g0207 a0002c0005t0001g0208 others(4): Show |
7 | HG02647.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.298+770G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3680764 | |||||||
chr2:3680767 | G | A | 2 | a0002c0002t0001g0142 a0002c0002t0002g0209 |
2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298+773G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3680767 | |||||||
chr2:3680774 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.298+780G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3680774 | |||||||
chr2:3680995 | T | A | 2 | a0002c0002t0001g0142 a0002c0002t0002g0209 |
2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299-639T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3680995 | |||||||
chr2:3681086 | G | A | 2 | a0002c0002t0001g0142 a0002c0002t0002g0209 |
2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299-548G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3681086 | |||||||
chr2:3681088 | T | C | 3 | a0002c0002t0002g0162 a0002c0002t0002g0210 a0002c0002t0002g0214 |
3 | HG02145.hp2 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.299-546T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3681088 | |||||||
chr2:3681159 | T | C | 26 | a0003c0003t0001g0005 a0003c0003t0001g0052 a0003c0003t0001g0115 others(23): Show |
31 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.299-475T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3681159 | |||||||
chr2:3681220 | C | T | 9 | a0002c0002t0002g0222 a0002c0013t0002g0031 a0003c0003t0002g0028 others(6): Show |
9 | HG02055.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-414C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3681220 | |||||||
chr2:3681573 | G | C | 3 | a0002c0002t0002g0162 a0002c0002t0002g0210 a0002c0002t0002g0214 |
3 | HG02145.hp2 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.299-61G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3681573 | |||||||
chr2:3681613 | G | T | 1 | a0008c0016t0002g0160 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.299-21G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3681613 | |||||||
chr2:3681618 | G | T | 1 | a0008c0016t0002g0160 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.299-16G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3681618 | |||||||
chr2:3681623 | T | C | 1 | a0008c0016t0002g0160 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.299-11T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3681623 | |||||||
chr2:3681625 | C | T | 1 | a0008c0016t0002g0160 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.299-9C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3681625 | |||||||
chr2:3681626 | A | G | 1 | a0008c0016t0002g0160 | 1 | NA19082.hp2 | splice_region_variant&intron_variant | LOW | c.299-8A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3681626 | |||||||
chr2:3681628 | C | A | 1 | a0008c0016t0002g0160 | 1 | NA19082.hp2 | splice_region_variant&intron_variant | LOW | c.299-6C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 5/11 | chr2 | 3681628 | |||||||
chr2:3681720 | C | T | 1 | a0008c0016t0002g0160 | 1 | NA19082.hp2 | splice_region_variant&intron_variant | LOW | c.378+7C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3681720 | |||||||
chr2:3681721 | T | G | 1 | a0008c0016t0002g0160 | 1 | NA19082.hp2 | splice_region_variant&intron_variant | LOW | c.378+8T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3681721 | |||||||
chr2:3681723 | C | G | 1 | a0008c0016t0002g0160 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.378+10C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3681723 | |||||||
chr2:3681781 | C | T | 2 | a0002c0002t0002g0222 a0002c0013t0002g0031 |
2 | HG02109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.378+68C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3681781 | |||||||
chr2:3681783 | C | T | 7 | a0003c0003t0002g0006 a0003c0003t0002g0015 a0003c0003t0002g0032 others(4): Show |
9 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.378+70C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3681783 | |||||||
chr2:3681879 | A | AT | 60 | a0003c0003t0001g0005 a0003c0003t0001g0038 a0003c0003t0001g0053 others(57): Show |
68 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.378+167dupT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 3681879 | ||||||
chr2:3681963 | C | T | 3 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.378+250C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3681963 | |||||||
chr2:3682038 | C | T | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.378+325C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682038 | |||||||
chr2:3682257 | C | T | 6 | a0003c0003t0002g0006 a0003c0003t0002g0015 a0003c0003t0002g0032 others(3): Show |
8 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+544C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682257 | |||||||
chr2:3682402 | C | G | 8 | a0002c0002t0002g0024 a0003c0003t0002g0006 a0003c0003t0002g0015 others(5): Show |
10 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.379-540C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682402 | |||||||
chr2:3682403 | C | G | 30 | a0003c0003t0001g0053 a0003c0003t0001g0065 a0003c0003t0001g0097 others(27): Show |
33 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.379-539C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682403 | |||||||
chr2:3682417 | G | C | 9 | a0003c0003t0001g0038 a0004c0004t0001g0035 a0004c0004t0001g0036 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-525G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682417 | |||||||
chr2:3682545 | G | A | 1 | a0003c0003t0002g0016 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.379-397G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682545 | |||||||
chr2:3682548 | C | T | 1 | a0003c0003t0002g0016 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.379-394C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682548 | |||||||
chr2:3682583 | G | T | 1 | a0003c0003t0002g0016 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.379-359G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682583 | |||||||
chr2:3682584 | G | C | 1 | a0003c0003t0002g0016 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.379-358G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682584 | |||||||
chr2:3682585 | G | A | 1 | a0003c0003t0002g0016 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.379-357G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682585 | |||||||
chr2:3682619 | A | G | 64 | a0001c0001t0001g0040 a0001c0001t0001g0125 a0001c0001t0001g0126 others(61): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.379-323A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682619 | |||||||
chr2:3682640 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0093 a0001c0001t0001g0102 |
4 | HG01192.hp1 HG01952.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-302C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682640 | |||||||
chr2:3682651 | G | A | 8 | a0002c0002t0002g0024 a0003c0003t0002g0006 a0003c0003t0002g0015 others(5): Show |
10 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.379-291G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682651 | |||||||
chr2:3682677 | C | T | 1 | a0004c0004t0002g0174 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.379-265C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682677 | |||||||
chr2:3682687 | G | A | 1 | a0004c0004t0002g0174 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.379-255G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682687 | |||||||
chr2:3682705 | C | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0092 a0002c0002t0002g0157 |
3 | HG00733.hp1 HG01993.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.379-237C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682705 | |||||||
chr2:3682711 | C | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0092 a0002c0002t0002g0157 |
3 | HG00733.hp1 HG01993.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.379-231C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682711 | |||||||
chr2:3682746 | C | G | 1 | a0002c0002t0002g0103 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.379-196C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682746 | |||||||
chr2:3682750 | C | T | 70 | a0002c0002t0001g0069 a0002c0002t0001g0071 a0002c0002t0001g0080 others(67): Show |
79 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.379-192C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682750 | |||||||
chr2:3682767 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.379-175C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682767 | |||||||
chr2:3682768 | G | A | 41 | a0002c0002t0001g0069 a0002c0002t0001g0071 a0002c0002t0001g0080 others(38): Show |
47 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.379-174G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682768 | |||||||
chr2:3682772 | G | A | 41 | a0002c0002t0001g0069 a0002c0002t0001g0071 a0002c0002t0001g0080 others(38): Show |
47 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.379-170G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682772 | |||||||
chr2:3682816 | T | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0003c0003t0001g0038 others(4): Show |
7 | HG02257.hp1 HG03130.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-126T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 6/11 | chr2 | 3682816 | |||||||
chr2:3683287 | A | T | 64 | a0002c0002t0001g0054 a0002c0002t0001g0069 a0002c0002t0001g0070 others(61): Show |
76 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.511+213A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3683287 | |||||||
chr2:3683330 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0055 others(7): Show |
11 | HG01074.hp2 HG01934.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.511+256A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3683330 | |||||||
chr2:3683924 | C | T | 3 | a0002c0002t0002g0222 a0002c0009t0002g0023 a0002c0013t0002g0031 |
3 | HG02109.hp1 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.511+850C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3683924 | |||||||
chr2:3684000 | TGACA | T | 8 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01109.hp2 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.511+931_511+934del others(4): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3684000 | ||||||
chr2:3684388 | T | G | 69 | a0001c0001t0001g0088 a0001c0001t0001g0107 a0001c0001t0001g0108 others(66): Show |
81 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.511+1314T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3684388 | |||||||
chr2:3684570 | C | G | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.511+1496C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3684570 | |||||||
chr2:3684956 | T | C | 44 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(41): Show |
47 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.511+1882T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3684956 | |||||||
chr2:3684997 | C | T | 64 | a0002c0002t0001g0054 a0002c0002t0001g0069 a0002c0002t0001g0070 others(61): Show |
76 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.511+1923C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3684997 | |||||||
chr2:3685214 | TCGCTAGC others(5214): Show |
T | 15 | a0002c0002t0001g0070 a0002c0002t0001g0109 a0002c0002t0002g0003 others(12): Show |
19 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.511+2142_512-5281d others(2): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3685214 | ||||||
chr2:3685215 | C | T | 1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.511+2141C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3685215 | |||||||
chr2:3685236 | C | CT | 44 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(41): Show |
47 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.511+2162_511+2163i others(3): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3685236 | |||||||
chr2:3685291 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.511+2217A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3685291 | |||||||
chr2:3685395 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.511+2321C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3685395 | |||||||
chr2:3685428 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.511+2354C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3685428 | |||||||
chr2:3685447 | C | CAG | 3 | a0003c0003t0001g0200 a0003c0003t0001g0201 a0003c0003t0002g0183 |
3 | HG01081.hp2 HG02071.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.511+2387_511+2388d others(4): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3685447 | ||||||
chr2:3685985 | T | A | 6 | a0003c0003t0002g0028 a0003c0003t0002g0030 a0003c0003t0002g0039 others(3): Show |
6 | HG02055.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.511+2911T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3685985 | |||||||
chr2:3686065 | C | T | 3 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.511+2991C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3686065 | |||||||
chr2:3686161 | T | A | 1 | a0001c0001t0001g0091 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.511+3087T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3686161 | |||||||
chr2:3686175 | C | A | 3 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0014t0002g0218 |
3 | HG02809.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.511+3101C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3686175 | |||||||
chr2:3686189 | C | T | 6 | a0003c0003t0002g0006 a0003c0003t0002g0015 a0003c0003t0002g0032 others(3): Show |
8 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.511+3115C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3686189 | |||||||
chr2:3686279 | G | T | 1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.511+3205G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3686279 | |||||||
chr2:3686354 | C | G | 107 | a0001c0001t0001g0040 a0002c0002t0001g0054 a0002c0002t0001g0069 others(104): Show |
118 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.511+3280C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3686354 | |||||||
chr2:3686373 | C | T | 59 | a0001c0001t0001g0040 a0002c0002t0001g0054 a0002c0002t0001g0069 others(56): Show |
67 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.511+3299C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3686373 | |||||||
chr2:3686409 | G | GT | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0003c0003t0001g0038 others(8): Show |
11 | HG02257.hp1 HG02258.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.511+3342dupT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3686409 | ||||||
chr2:3686447 | T | G | 36 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(33): Show |
39 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.511+3373T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3686447 | |||||||
chr2:3686535 | T | C | 13 | a0002c0005t0001g0206 a0002c0005t0001g0207 a0002c0005t0001g0208 others(10): Show |
13 | HG02055.hp1 HG02451.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.511+3461T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3686535 | |||||||
chr2:3686574 | C | T | 49 | a0002c0002t0001g0054 a0002c0002t0001g0069 a0002c0002t0001g0071 others(46): Show |
57 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.511+3500C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3686574 | |||||||
chr2:3686575 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.511+3501G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3686575 | |||||||
chr2:3686815 | GT | G | 3 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.511+3744delT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3686815 | ||||||
chr2:3687366 | C | T | 33 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(30): Show |
36 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.511+4292C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3687366 | |||||||
chr2:3687546 | G | T | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.511+4472G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3687546 | |||||||
chr2:3687590 | T | G | 70 | a0001c0001t0001g0088 a0001c0001t0001g0107 a0001c0001t0001g0108 others(67): Show |
78 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.511+4516T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3687590 | |||||||
chr2:3687659 | A | C | 3 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.511+4585A>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3687659 | |||||||
chr2:3687665 | G | C | 71 | a0001c0001t0001g0040 a0001c0001t0001g0088 a0001c0001t0001g0107 others(68): Show |
79 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.511+4591G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3687665 | |||||||
chr2:3687769 | G | A | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0003c0003t0001g0038 others(8): Show |
11 | HG02257.hp1 HG02258.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.511+4695G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3687769 | |||||||
chr2:3687884 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.511+4810A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3687884 | |||||||
chr2:3687898 | G | A | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0003c0003t0001g0038 others(8): Show |
11 | HG02257.hp1 HG02258.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.511+4824G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3687898 | |||||||
chr2:3687915 | G | A | 33 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(30): Show |
36 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.511+4841G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3687915 | |||||||
chr2:3688236 | A | G | 123 | a0001c0001t0001g0040 a0001c0001t0001g0088 a0001c0001t0001g0107 others(120): Show |
134 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(131): Show |
intron_variant | MODIFIER | c.511+5162A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3688236 | |||||||
chr2:3688500 | C | T | 1 | a0003c0003t0002g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511+5426C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3688500 | |||||||
chr2:3688526 | T | C | 1 | a0003c0010t0004g0228 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.511+5452T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3688526 | |||||||
chr2:3688716 | C | T | 3 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0014t0002g0218 |
3 | HG02809.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.511+5642C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3688716 | |||||||
chr2:3688892 | G | A | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0003c0003t0001g0038 others(8): Show |
11 | HG02257.hp1 HG02258.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.511+5818G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3688892 | |||||||
chr2:3689326 | T | C | 1 | a0004c0004t0002g0110 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.511+6252T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3689326 | |||||||
chr2:3689396 | T | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0003c0003t0001g0038 others(4): Show |
7 | HG02257.hp1 HG03130.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.512-6321T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3689396 | |||||||
chr2:3689505 | G | T | 3 | a0002c0002t0002g0222 a0002c0009t0002g0023 a0002c0013t0002g0031 |
3 | HG02109.hp1 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.512-6212G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3689505 | |||||||
chr2:3689525 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0091 a0001c0001t0001g0100 |
3 | HG01074.hp2 HG01934.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.512-6192C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3689525 | |||||||
chr2:3689538 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.512-6179T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3689538 | |||||||
chr2:3689637 | C | A | 3 | a0003c0003t0002g0123 a0006c0008t0002g0181 a0006c0008t0003g0231 |
3 | HG02717.hp1 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.512-6080C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3689637 | |||||||
chr2:3689834 | T | C | 1 | a0001c0001t0002g0020 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.512-5883T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3689834 | |||||||
chr2:3689835 | C | T | 1 | a0001c0001t0002g0020 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.512-5882C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3689835 | |||||||
chr2:3689947 | C | CT | 93 | a0001c0001t0001g0040 a0002c0002t0001g0069 a0002c0002t0001g0071 others(90): Show |
104 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.512-5757dupT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3689947 | ||||||
chr2:3689947 | CT | C | 16 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0125 others(13): Show |
16 | HG01168.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.512-5757delT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3689947 | ||||||
chr2:3690246 | C | A | 3 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.512-5471C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690246 | |||||||
chr2:3690257 | C | T | 1 | a0002c0002t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.512-5460C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690257 | |||||||
chr2:3690260 | T | C | 13 | a0002c0005t0001g0206 a0002c0005t0001g0207 a0002c0005t0001g0208 others(10): Show |
13 | HG02055.hp1 HG02451.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.512-5457T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690260 | |||||||
chr2:3690261 | T | C | 3 | a0002c0002t0002g0134 a0002c0014t0002g0218 a0003c0003t0002g0221 |
3 | HG01891.hp2 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.512-5456T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690261 | |||||||
chr2:3690266 | C | CCCCCCT | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0003c0003t0001g0038 others(7): Show |
10 | HG02257.hp1 HG02258.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.512-5446_512-5441d others(8): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690266 | ||||||
chr2:3690267 | C | A | 1 | a0003c0003t0001g0005 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.512-5450C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690267 | |||||||
chr2:3690267 | C | CCCCCTCC others(17): Show |
1 | a0003c0003t0002g0183 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.512-5441_512-5440i others(26): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690267 | ||||||
chr2:3690267 | C | CCCCCTCC others(580): Show |
1 | a0005c0007t0004g0226 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.512-5441_512-5440i others(589): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690267 | ||||||
chr2:3690272 | T | C | 1 | a0002c0002t0002g0155 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.512-5445T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690272 | |||||||
chr2:3690272 | T | TC | 33 | a0002c0002t0001g0142 a0002c0002t0002g0209 a0002c0002t0002g0210 others(30): Show |
36 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.512-5441dupC | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690272 | ||||||
chr2:3690272 | T | TCCCCCTC others(523): Show |
1 | a0005c0007t0004g0225 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.512-5441_512-5440i others(532): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690272 | ||||||
chr2:3690273 | CCCCTCCC others(26): Show |
C | 1 | a0001c0001t0001g0143 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.512-5440_512-5408d others(35): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690273 | ||||||
chr2:3690277 | T | TCCCCCTC others(334): Show |
1 | a0003c0003t0002g0211 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.512-5424_512-5423i others(343): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690277 | ||||||
chr2:3690278 | C | CCCCCTCC others(194): Show |
1 | a0003c0003t0002g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.512-5429_512-5428i others(203): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690278 | ||||||
chr2:3690278 | C | CCCCCTCC others(516): Show |
1 | a0002c0005t0002g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.512-5424_512-5423i others(525): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690278 | ||||||
chr2:3690278 | C | CCCCCTCC others(16): Show |
2 | a0001c0001t0001g0083 a0001c0001t0001g0166 |
2 | HG00544.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.512-5405_512-5383d others(25): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690278 | ||||||
chr2:3690278 | C | CCCCCTCC others(68): Show |
1 | a0003c0003t0002g0015 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.512-5419_512-5418i others(77): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690278 | ||||||
chr2:3690278 | C | CCCCCTCC others(47): Show |
1 | a0002c0002t0002g0024 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.512-5419_512-5418i others(56): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690278 | ||||||
chr2:3690278 | C | CCCCCTCC others(42): Show |
7 | a0003c0003t0001g0005 a0003c0003t0001g0117 a0003c0003t0001g0119 others(4): Show |
9 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.512-5419_512-5418i others(51): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690278 | ||||||
chr2:3690278 | C | CCCCCTCC others(65): Show |
1 | a0003c0003t0001g0115 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.512-5419_512-5418i others(74): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690278 | ||||||
chr2:3690278 | C | CCCCCTCC others(41): Show |
1 | a0003c0003t0001g0005 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.512-5419_512-5418i others(50): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690278 | ||||||
chr2:3690278 | C | CCCCTCCC others(79): Show |
1 | a0004c0004t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.512-5436_512-5435i others(88): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690278 | ||||||
chr2:3690278 | C | CCCCTCCC others(85): Show |
1 | a0002c0014t0002g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.512-5436_512-5435i others(94): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690278 | ||||||
chr2:3690278 | C | CCTCTTCC others(43): Show |
1 | a0002c0009t0002g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.512-5438_512-5437i others(52): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690278 | ||||||
chr2:3690278 | C | CCTCTTCC others(220): Show |
1 | a0005c0007t0004g0229 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.512-5438_512-5437i others(229): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690278 | ||||||
chr2:3690280 | C | T | 31 | a0002c0002t0001g0142 a0002c0002t0002g0209 a0002c0002t0002g0210 others(28): Show |
34 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.512-5437C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690280 | |||||||
chr2:3690282 | C | T | 33 | a0002c0002t0001g0142 a0002c0002t0002g0209 a0002c0002t0002g0210 others(30): Show |
36 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.512-5435C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690282 | |||||||
chr2:3690283 | T | C | 14 | a0001c0001t0001g0088 a0001c0001t0001g0125 a0001c0001t0001g0126 others(11): Show |
14 | HG01123.hp2 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.512-5434T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690283 | |||||||
chr2:3690283 | T | TCCCCCTC others(435): Show |
1 | a0003c0003t0002g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.512-5424_512-5423i others(444): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690283 | ||||||
chr2:3690283 | T | TCCCCCTC others(30): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0099 |
2 | HG04184.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.512-5417_512-5416i others(39): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690283 | ||||||
chr2:3690283 | T | TCCCCCTC others(28): Show |
14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(11): Show |
19 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.512-5405_512-5371d others(37): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690283 | ||||||
chr2:3690283 | T | TCCCCCTC others(51): Show |
1 | a0004c0004t0002g0173 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.512-5383_512-5382i others(60): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690283 | ||||||
chr2:3690283 | T | TCCCCTCC others(23): Show |
1 | a0001c0001t0001g0002 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.512-5430_512-5429i others(32): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690283 | ||||||
chr2:3690284 | C | CCCCCTCC others(369): Show |
1 | a0002c0005t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.512-5424_512-5423i others(378): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690284 | ||||||
chr2:3690284 | C | CCCCCTCC others(368): Show |
1 | a0002c0005t0001g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.512-5424_512-5423i others(377): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690284 | ||||||
chr2:3690284 | C | CCCCTCCC others(14): Show |
1 | a0002c0002t0002g0062 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.512-5430_512-5429i others(23): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690284 | ||||||
chr2:3690284 | C | T | 12 | a0001c0001t0001g0088 a0001c0001t0001g0125 a0001c0001t0001g0126 others(9): Show |
12 | HG02257.hp1 HG02258.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.512-5433C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690284 | |||||||
chr2:3690289 | T | TC | 6 | a0002c0005t0001g0206 a0002c0005t0001g0208 a0002c0005t0002g0047 others(3): Show |
6 | HG02451.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.512-5424dupC | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690289 | ||||||
chr2:3690289 | T | TCCCCCTC others(606): Show |
1 | a0003c0003t0002g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.512-5424_512-5423i others(615): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690289 | ||||||
chr2:3690289 | T | TCCCTCCC others(9): Show |
1 | a0008c0016t0002g0160 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.512-5425_512-5424i others(18): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690289 | ||||||
chr2:3690293 | C | CCTCCCCC others(12): Show |
1 | a0001c0001t0001g0001 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.512-5424_512-5423i others(21): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690293 | |||||||
chr2:3690294 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0108 a0002c0002t0002g0214 others(1): Show |
5 | HG00741.hp1 HG01515.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.512-5423T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690294 | |||||||
chr2:3690295 | C | CCCCCTCC others(33): Show |
1 | a0002c0002t0001g0081 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.512-5418_512-5417i others(42): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690295 | ||||||
chr2:3690295 | C | CCCCT | 7 | a0002c0002t0001g0086 a0002c0002t0001g0202 a0002c0002t0002g0175 others(4): Show |
7 | HG02080.hp1 HG02083.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.512-5419_512-5418i others(6): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690295 | ||||||
chr2:3690295 | C | CCCCTCCC others(29): Show |
1 | a0002c0002t0001g0080 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.512-5419_512-5418i others(38): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690295 | ||||||
chr2:3690295 | C | CCCCTCCC others(53): Show |
2 | a0003c0003t0001g0052 a0003c0003t0001g0116 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.512-5419_512-5418i others(62): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690295 | ||||||
chr2:3690295 | C | T | 2 | a0002c0002t0002g0214 a0003c0003t0001g0201 |
2 | HG02148.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.512-5422C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690295 | |||||||
chr2:3690295 | CCCCCCTC others(4): Show |
C | 1 | a0001c0001t0001g0077 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.512-5405_512-5395d others(13): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690295 | ||||||
chr2:3690296 | C | CCCTCCCC others(2): Show |
9 | a0002c0002t0001g0069 a0002c0002t0002g0019 a0002c0002t0002g0060 others(6): Show |
9 | HG01123.hp1 HG01891.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.512-5419_512-5418i others(11): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(81): Show |
2 | a0003c0003t0002g0168 a0003c0003t0002g0176 |
2 | NA19007.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.512-5419_512-5418i others(90): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(90): Show |
1 | a0003c0003t0002g0016 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.512-5419_512-5418i others(99): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(95): Show |
1 | a0002c0002t0001g0142 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.512-5419_512-5418i others(104): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(512): Show |
1 | a0002c0005t0001g0208 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.512-5419_512-5418i others(521): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(609): Show |
1 | a0002c0005t0002g0047 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.512-5419_512-5418i others(618): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(19): Show |
1 | a0002c0002t0001g0095 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.512-5419_512-5418i others(28): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(577): Show |
1 | a0003c0003t0002g0048 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.512-5419_512-5418i others(586): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(554): Show |
1 | a0003c0003t0002g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.512-5419_512-5418i others(563): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(18): Show |
12 | a0002c0002t0001g0054 a0002c0002t0001g0071 a0002c0002t0001g0085 others(9): Show |
14 | HG00280.hp2 HG00639.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.512-5419_512-5418i others(27): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(272): Show |
1 | a0003c0003t0002g0159 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.512-5419_512-5418i others(281): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(283): Show |
1 | a0003c0003t0002g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.512-5419_512-5418i others(292): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(283): Show |
1 | a0003c0003t0002g0006 | 2 | HG01243.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.512-5419_512-5418i others(292): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(256): Show |
2 | a0003c0003t0002g0032 a0003c0003t0002g0150 |
2 | HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.512-5419_512-5418i others(265): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(28): Show |
1 | a0002c0002t0002g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.512-5419_512-5418i others(37): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(34): Show |
1 | a0002c0002t0002g0151 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.512-5419_512-5418i others(43): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(17): Show |
1 | a0002c0002t0002g0103 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.512-5419_512-5418i others(26): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690296 | C | CCCTCCCC others(100): Show |
1 | a0002c0002t0002g0061 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.512-5419_512-5418i others(109): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690296 | ||||||
chr2:3690299 | C | T | 25 | a0002c0002t0002g0133 a0002c0002t0002g0209 a0002c0002t0002g0210 others(22): Show |
27 | HG00735.hp2 HG01361.hp2 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.512-5418C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690299 | |||||||
chr2:3690300 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.512-5417C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690300 | |||||||
chr2:3690300 | CT | C | 23 | a0002c0002t0002g0209 a0002c0002t0002g0210 a0002c0002t0002g0222 others(20): Show |
25 | HG00735.hp2 HG01361.hp2 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.512-5416delT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690300 | |||||||
chr2:3690301 | T | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0002c0002t0002g0133 others(2): Show |
5 | HG01256.hp1 HG01515.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.512-5416T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690301 | |||||||
chr2:3690301 | T | TCCCCTCC others(25): Show |
1 | a0001c0001t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.512-5406_512-5405i others(34): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690301 | ||||||
chr2:3690305 | C | CCCCCCCT others(17): Show |
1 | a0001c0001t0001g0199 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.512-5412_512-5411i others(26): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690305 | |||||||
chr2:3690306 | T | C | 6 | a0001c0001t0001g0199 a0002c0002t0002g0162 a0002c0013t0002g0031 others(3): Show |
6 | HG02451.hp2 HG02895.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.512-5411T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690306 | |||||||
chr2:3690306 | T | TC | 9 | a0001c0001t0001g0002 a0002c0002t0001g0080 a0002c0002t0001g0081 others(6): Show |
9 | HG01109.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.512-5406dupC | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690306 | ||||||
chr2:3690306 | T | TCCCCCTC others(6): Show |
1 | a0001c0001t0001g0007 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.512-5401_512-5400i others(15): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690306 | ||||||
chr2:3690306 | T | TCCCCCTC others(5): Show |
2 | a0001c0001t0001g0074 a0001c0001t0001g0076 |
2 | NA18965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.512-5371_512-5360d others(14): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690306 | ||||||
chr2:3690306 | T | TCCCCCTC others(17): Show |
5 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0203 others(2): Show |
6 | HG01074.hp2 HG02293.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.512-5383_512-5360d others(26): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690306 | ||||||
chr2:3690306 | T | TCCCCCTC others(29): Show |
1 | a0001c0001t0001g0091 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.512-5395_512-5360d others(38): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690306 | ||||||
chr2:3690306 | T | TCCCCCTC others(40): Show |
1 | a0001c0001t0001g0001 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.512-5371_512-5370i others(49): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690306 | ||||||
chr2:3690306 | T | TCCCCTCC others(187): Show |
1 | a0002c0002t0002g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.512-5407_512-5406i others(196): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690306 | ||||||
chr2:3690306 | TCCCCCTC others(5): Show |
T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0064 others(6): Show |
9 | HG00323.hp1 HG00735.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.512-5371_512-5360d others(14): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690306 | ||||||
chr2:3690307 | C | CCCCCTCC others(72): Show |
1 | a0001c0001t0001g0089 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.512-5360_512-5359i others(81): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690307 | ||||||
chr2:3690307 | C | T | 5 | a0002c0002t0002g0162 a0002c0013t0002g0031 a0003c0003t0001g0053 others(2): Show |
5 | HG02451.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.512-5410C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690307 | |||||||
chr2:3690307 | CCCCCTCC others(34): Show |
C | 2 | a0002c0006t0001g0041 a0002c0006t0001g0141 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.512-5394_512-5354d others(43): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690307 | ||||||
chr2:3690311 | C | T | 1 | a0003c0003t0002g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.512-5406C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690311 | |||||||
chr2:3690312 | T | C | 3 | a0003c0003t0002g0015 a0003c0003t0002g0028 a0005c0007t0004g0225 |
3 | HG01123.hp2 HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.512-5405T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690312 | |||||||
chr2:3690312 | T | TC | 4 | a0003c0003t0001g0200 a0003c0003t0001g0201 a0003c0003t0002g0123 others(1): Show |
4 | HG01081.hp2 HG02071.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-5401dupC | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690312 | ||||||
chr2:3690317 | T | C | 4 | a0002c0005t0001g0206 a0002c0013t0002g0031 a0006c0008t0002g0181 others(1): Show |
4 | HG02717.hp1 HG03540.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.512-5400T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690317 | |||||||
chr2:3690317 | T | TCCCCCCT others(18): Show |
1 | a0001c0001t0001g0100 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.512-5394_512-5370d others(27): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690317 | ||||||
chr2:3690317 | TC | T | 8 | a0001c0001t0001g0143 a0002c0002t0002g0061 a0002c0002t0002g0134 others(5): Show |
8 | HG01168.hp1 HG01975.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.512-5394delC | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690317 | ||||||
chr2:3690317 | TCCCCCCT others(7): Show |
T | 1 | a0004c0004t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.512-5395_512-5382d others(16): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690317 | ||||||
chr2:3690318 | C | CCCCCCTC others(16): Show |
1 | a0001c0001t0001g0001 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.512-5393_512-5371d others(25): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690318 | ||||||
chr2:3690318 | C | CCCCT | 14 | a0002c0002t0001g0069 a0002c0002t0001g0086 a0002c0002t0001g0202 others(11): Show |
14 | HG01123.hp1 HG01891.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.512-5396_512-5395i others(6): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690318 | ||||||
chr2:3690318 | C | CCCCTCCC others(30): Show |
1 | a0003c0010t0004g0228 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.512-5396_512-5395i others(39): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690318 | ||||||
chr2:3690318 | C | T | 3 | a0002c0013t0002g0031 a0006c0008t0002g0181 a0006c0008t0003g0231 |
3 | HG02717.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.512-5399C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690318 | |||||||
chr2:3690319 | C | CCCCT | 25 | a0002c0002t0002g0209 a0002c0002t0002g0210 a0002c0005t0002g0022 others(22): Show |
27 | HG00735.hp2 HG01243.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.512-5395_512-5394i others(6): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690319 | ||||||
chr2:3690319 | C | CCCCTCCC others(54): Show |
1 | a0002c0002t0002g0222 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.512-5395_512-5394i others(63): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690319 | ||||||
chr2:3690319 | C | CCCTCCCC others(39): Show |
8 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0003c0003t0001g0038 others(5): Show |
8 | HG02257.hp1 HG02723.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.512-5396_512-5395i others(48): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690319 | ||||||
chr2:3690319 | C | CCCTCCCC others(44): Show |
1 | a0004c0004t0001g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.512-5396_512-5395i others(53): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690319 | ||||||
chr2:3690319 | C | T | 2 | a0002c0002t0002g0162 a0003c0003t0002g0211 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.512-5398C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690319 | |||||||
chr2:3690319 | CCCCCT | C | 8 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01109.hp2 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.512-5388_512-5384d others(7): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690319 | ||||||
chr2:3690322 | C | T | 8 | a0002c0002t0001g0205 a0002c0005t0001g0208 a0002c0005t0002g0047 others(5): Show |
8 | HG01081.hp2 HG02071.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.512-5395C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690322 | |||||||
chr2:3690323 | C | T | 1 | a0003c0003t0002g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.512-5394C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690323 | |||||||
chr2:3690324 | T | C | 9 | a0002c0002t0001g0205 a0002c0005t0001g0208 a0002c0005t0002g0047 others(6): Show |
9 | HG01081.hp2 HG02071.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.512-5393T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690324 | |||||||
chr2:3690325 | C | T | 1 | a0002c0002t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.512-5392C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690325 | |||||||
chr2:3690329 | T | C | 2 | a0002c0005t0001g0206 a0003c0003t0001g0053 |
2 | HG03540.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.512-5388T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690329 | |||||||
chr2:3690330 | C | CCCCCCCT others(342): Show |
1 | a0005c0007t0004g0229 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.512-5382_512-5381i others(351): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690330 | ||||||
chr2:3690330 | C | CCCCTCCC others(64): Show |
1 | a0005c0007t0004g0225 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.512-5384_512-5383i others(73): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690330 | ||||||
chr2:3690331 | C | CCCCCCCC others(349): Show |
1 | a0006c0008t0002g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.512-5382_512-5381i others(358): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690331 | ||||||
chr2:3690331 | C | CCCTCCCC others(214): Show |
1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.512-5384_512-5383i others(223): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690331 | ||||||
chr2:3690331 | C | T | 1 | a0003c0003t0001g0053 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.512-5386C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690331 | |||||||
chr2:3690334 | C | T | 3 | a0003c0003t0002g0026 a0003c0003t0002g0027 a0003c0003t0002g0048 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.512-5383C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690334 | |||||||
chr2:3690335 | C | T | 3 | a0002c0005t0001g0208 a0002c0005t0002g0047 a0002c0013t0002g0031 |
3 | HG02818.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.512-5382C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690335 | |||||||
chr2:3690336 | T | C | 26 | a0002c0002t0002g0162 a0002c0002t0002g0210 a0002c0005t0001g0208 others(23): Show |
28 | HG00735.hp2 HG01361.hp2 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.512-5381T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690336 | |||||||
chr2:3690338 | C | T | 17 | a0002c0002t0002g0162 a0002c0002t0002g0210 a0003c0003t0001g0065 others(14): Show |
18 | HG00735.hp2 HG01361.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.512-5379C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690338 | |||||||
chr2:3690341 | T | C | 21 | a0002c0002t0002g0162 a0002c0002t0002g0210 a0003c0003t0001g0065 others(18): Show |
22 | HG00735.hp2 HG01361.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.512-5376T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690341 | |||||||
chr2:3690341 | T | TCCCCCCT others(18): Show |
1 | a0001c0001t0001g0055 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.512-5360_512-5359i others(27): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690341 | ||||||
chr2:3690342 | C | CCCCCTCC others(3): Show |
5 | a0003c0003t0002g0006 a0003c0003t0002g0032 a0003c0003t0002g0033 others(2): Show |
6 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.512-5371_512-5370i others(12): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690342 | ||||||
chr2:3690342 | C | CCCCTCCC others(121): Show |
1 | a0002c0002t0002g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.512-5372_512-5371i others(130): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690342 | ||||||
chr2:3690343 | C | CCCCTCCC others(59): Show |
1 | a0001c0001t0001g0002 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.512-5371_512-5370i others(68): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690343 | ||||||
chr2:3690343 | C | CCCTCCCC others(3): Show |
1 | a0003c0003t0002g0211 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.512-5372_512-5371i others(12): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690343 | ||||||
chr2:3690343 | C | T | 21 | a0002c0002t0002g0162 a0002c0002t0002g0210 a0003c0003t0001g0065 others(18): Show |
22 | HG00735.hp2 HG01361.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.512-5374C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690343 | |||||||
chr2:3690346 | C | CTCCCCTC others(23): Show |
1 | a0001c0001t0001g0184 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.512-5371_512-5370i others(32): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690346 | |||||||
chr2:3690346 | C | T | 14 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0002c0002t0001g0205 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.512-5371C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690346 | |||||||
chr2:3690348 | T | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0125 a0001c0001t0001g0126 others(11): Show |
14 | HG02257.hp1 HG02723.hp1 HG03130.hp2 others(11): Show |
intron_variant | MODIFIER | c.512-5369T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690348 | |||||||
chr2:3690348 | T | TCCCCTC | 1 | a0003c0003t0001g0005 | 3 | HG00323.hp2 HG01106.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.512-5365_512-5360d others(8): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690348 | ||||||
chr2:3690348 | T | TCCCCTCC | 25 | a0001c0001t0001g0007 a0002c0002t0001g0071 a0002c0002t0001g0085 others(22): Show |
26 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.512-5366_512-5360d others(9): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690348 | ||||||
chr2:3690348 | T | TCCCCTCC others(12): Show |
1 | a0001c0001t0001g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.512-5360_512-5359i others(21): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690348 | ||||||
chr2:3690348 | T | TCCCCTCC others(44): Show |
1 | a0002c0002t0002g0152 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.512-5360_512-5359i others(53): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690348 | ||||||
chr2:3690348 | T | TCCCCTCC others(87): Show |
1 | a0002c0002t0002g0103 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.512-5360_512-5359i others(96): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690348 | ||||||
chr2:3690348 | T | TCCCCTCC others(41): Show |
1 | a0001c0001t0001g0001 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.512-5360_512-5359i others(50): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690348 | ||||||
chr2:3690348 | T | TCCCCTCC others(249): Show |
1 | a0002c0009t0002g0023 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.512-5354_512-5353i others(258): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690348 | ||||||
chr2:3690352 | C | G | 1 | a0002c0002t0002g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.512-5365C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690352 | |||||||
chr2:3690353 | T | TCCCCCCC others(106): Show |
1 | a0002c0002t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.512-5360_512-5359i others(115): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690353 | ||||||
chr2:3690353 | T | TCCCCCCT others(95): Show |
1 | a0002c0002t0001g0069 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.512-5360_512-5359i others(104): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690353 | ||||||
chr2:3690353 | T | TCCCCCCT others(83): Show |
1 | a0002c0002t0002g0019 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.512-5360_512-5359i others(92): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690353 | ||||||
chr2:3690353 | T | TCCCCCCT others(93): Show |
1 | a0002c0002t0002g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.512-5360_512-5359i others(102): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690353 | ||||||
chr2:3690353 | T | TCCCCCTC others(295): Show |
1 | a0003c0003t0002g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.512-5360_512-5359i others(304): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690353 | ||||||
chr2:3690353 | T | TCCCCCTC others(216): Show |
1 | a0003c0003t0002g0015 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.512-5360_512-5359i others(225): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690353 | ||||||
chr2:3690353 | T | TCCCCCTC others(182): Show |
1 | a0002c0002t0002g0024 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.512-5360_512-5359i others(191): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690353 | ||||||
chr2:3690358 | T | C | 10 | a0001c0001t0001g0002 a0002c0002t0001g0054 a0002c0002t0002g0004 others(7): Show |
12 | HG01123.hp1 HG02004.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.512-5359T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690358 | |||||||
chr2:3690358 | T | TCCCCCCT others(161): Show |
1 | a0002c0005t0001g0215 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.512-5354_512-5353i others(170): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690358 | ||||||
chr2:3690358 | T | TCCCCCCT others(159): Show |
1 | a0002c0005t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.512-5354_512-5353i others(168): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690358 | ||||||
chr2:3690358 | T | TCCCCCTC others(37): Show |
1 | a0002c0006t0002g0135 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.512-5338_512-5295d others(46): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690358 | ||||||
chr2:3690359 | C | CT | 3 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0003c0003t0002g0048 |
3 | HG01109.hp1 HG01978.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.512-5358_512-5357i others(3): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690359 | |||||||
chr2:3690359 | C | CTCCCCTC others(54): Show |
2 | a0002c0002t0002g0128 a0002c0002t0002g0194 |
2 | HG01123.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.512-5358_512-5357i others(63): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690359 | |||||||
chr2:3690359 | C | CTCCCCTC others(59): Show |
1 | a0002c0002t0002g0149 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.512-5358_512-5357i others(68): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690359 | |||||||
chr2:3690359 | C | CTCCCCTC others(43): Show |
1 | a0002c0002t0002g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.512-5358_512-5357i others(52): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690359 | |||||||
chr2:3690359 | C | CTCCCCTC others(74): Show |
1 | a0002c0002t0002g0060 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.512-5358_512-5357i others(83): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690359 | |||||||
chr2:3690359 | C | T | 3 | a0001c0001t0001g0002 a0002c0002t0001g0054 a0002c0002t0002g0004 |
5 | HG02004.hp2 HG02015.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.512-5358C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690359 | |||||||
chr2:3690359 | CCCCCT | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0056 others(1): Show |
4 | HG01106.hp2 HG01517.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.512-5333_512-5329d others(7): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690359 | ||||||
chr2:3690360 | C | CCCTCCCC others(57): Show |
1 | a0002c0015t0002g0059 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.512-5355_512-5354i others(66): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690360 | ||||||
chr2:3690362 | C | A | 15 | a0002c0002t0002g0162 a0002c0002t0002g0210 a0002c0002t0002g0214 others(12): Show |
17 | HG00735.hp2 HG01361.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.512-5355C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690362 | |||||||
chr2:3690362 | C | CCCTCCCC others(503): Show |
1 | a0002c0005t0001g0206 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.512-5354_512-5353i others(512): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690362 | ||||||
chr2:3690362 | C | CT | 11 | a0001c0001t0001g0040 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG02257.hp1 HG02723.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.512-5355_512-5354i others(3): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690362 | |||||||
chr2:3690363 | C | CCTCCCCT | 5 | a0003c0003t0002g0006 a0003c0003t0002g0032 a0003c0003t0002g0033 others(2): Show |
6 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.512-5354_512-5353i others(9): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690363 | |||||||
chr2:3690363 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0046 others(7): Show |
11 | HG01975.hp2 HG02109.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.512-5354C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690363 | |||||||
chr2:3690364 | T | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0040 others(25): Show |
30 | HG01243.hp2 HG01891.hp1 HG01975.hp2 others(27): Show |
intron_variant | MODIFIER | c.512-5353T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690364 | |||||||
chr2:3690366 | C | A | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0003c0003t0001g0038 others(6): Show |
9 | HG02257.hp1 HG02723.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.512-5351C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690366 | |||||||
chr2:3690369 | T | TC | 5 | a0002c0002t0001g0142 a0002c0002t0002g0134 a0002c0002t0002g0209 others(2): Show |
5 | HG02818.hp2 HG02886.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.512-5344dupC | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690369 | ||||||
chr2:3690369 | T | TCCCCTCC others(5): Show |
1 | a0001c0001t0001g0088 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.512-5345_512-5334d others(14): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690369 | ||||||
chr2:3690369 | T | TCCCCTCC others(63): Show |
1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.512-5334_512-5333i others(72): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690369 | ||||||
chr2:3690369 | T | TCCCCTCC others(10): Show |
1 | a0001c0001t0002g0154 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.512-5310_512-5294d others(19): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690369 | ||||||
chr2:3690372 | C | CCCTCCCC others(13): Show |
1 | a0001c0001t0001g0001 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.512-5344_512-5343i others(22): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690372 | ||||||
chr2:3690372 | C | CCCTCCCC others(120): Show |
1 | a0003c0003t0002g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.512-5344_512-5343i others(129): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690372 | ||||||
chr2:3690372 | C | T | 1 | a0003c0003t0002g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.512-5345C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690372 | |||||||
chr2:3690373 | C | CCTCCCCT others(456): Show |
1 | a0003c0010t0004g0228 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.512-5344_512-5343i others(465): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690373 | |||||||
chr2:3690374 | T | C | 5 | a0003c0003t0002g0016 a0003c0003t0002g0030 a0003c0003t0002g0039 others(2): Show |
6 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.512-5343T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690374 | |||||||
chr2:3690374 | T | CCCCCTCC others(36): Show |
1 | a0001c0001t0001g0001 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.512-5386_512-5344d others(45): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690374 | |||||||
chr2:3690374 | T | TC | 12 | a0002c0002t0002g0060 a0002c0002t0002g0128 a0002c0002t0002g0133 others(9): Show |
12 | HG01123.hp1 HG01123.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.512-5339dupC | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690374 | ||||||
chr2:3690374 | T | TCC | 11 | a0001c0001t0001g0040 a0002c0005t0001g0207 a0002c0005t0001g0208 others(8): Show |
11 | HG01081.hp2 HG02071.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.512-5340_512-5339d others(4): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690374 | ||||||
chr2:3690374 | T | TCCCCTCC others(36): Show |
1 | a0002c0002t0002g0004 | 3 | HG03490.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.512-5334_512-5333i others(45): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690374 | ||||||
chr2:3690378 | C | CCCTCCCC others(375): Show |
1 | a0003c0003t0002g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.512-5339_512-5338i others(384): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690378 | |||||||
chr2:3690379 | T | C | 1 | a0003c0003t0002g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.512-5338T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690379 | |||||||
chr2:3690379 | T | TCCCCCTC others(31): Show |
1 | a0002c0002t0001g0054 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.512-5334_512-5333i others(40): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690379 | ||||||
chr2:3690379 | T | TCCCCTCC others(90): Show |
1 | a0002c0002t0002g0062 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.512-5328_512-5327i others(99): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690379 | ||||||
chr2:3690383 | C | A | 1 | a0004c0004t0001g0037 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.512-5334C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690383 | |||||||
chr2:3690384 | T | C | 4 | a0002c0002t0002g0103 a0002c0002t0002g0155 a0002c0014t0002g0218 others(1): Show |
4 | HG03041.hp1 HG04228.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-5333T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690384 | |||||||
chr2:3690384 | T | TCCCCCTC others(87): Show |
1 | a0002c0002t0002g0186 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.512-5328_512-5327i others(96): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690384 | ||||||
chr2:3690384 | T | TCCCCCTC others(89): Show |
1 | a0003c0003t0001g0115 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.512-5328_512-5327i others(98): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690384 | ||||||
chr2:3690384 | T | TCCCCCTC others(90): Show |
7 | a0003c0003t0001g0005 a0003c0003t0001g0052 a0003c0003t0001g0116 others(4): Show |
8 | HG00323.hp2 HG00642.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.512-5328_512-5327i others(99): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690384 | ||||||
chr2:3690384 | T | TCCCCCTC others(91): Show |
1 | a0003c0003t0001g0117 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.512-5328_512-5327i others(100): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690384 | ||||||
chr2:3690384 | T | TCCCCCTC others(92): Show |
1 | a0003c0003t0002g0014 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.512-5328_512-5327i others(101): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690384 | ||||||
chr2:3690384 | TC | T | 17 | a0002c0002t0001g0071 a0002c0002t0001g0085 a0002c0002t0001g0086 others(14): Show |
17 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.512-5327delC | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690384 | ||||||
chr2:3690385 | C | CCCCCTCC others(56): Show |
1 | a0003c0003t0001g0053 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.512-5328_512-5327i others(65): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690385 | ||||||
chr2:3690385 | C | CCCCCTCC others(73): Show |
1 | a0003c0003t0001g0005 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.512-5328_512-5327i others(82): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690385 | ||||||
chr2:3690385 | C | CCCCCTCC others(52): Show |
1 | a0006c0008t0002g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.512-5328_512-5327i others(61): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690385 | ||||||
chr2:3690385 | C | CCCCT | 11 | a0002c0002t0001g0080 a0003c0003t0001g0097 a0003c0003t0001g0098 others(8): Show |
12 | HG01070.hp1 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.512-5329_512-5328i others(6): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690385 | ||||||
chr2:3690385 | C | CCCCTCCC others(400): Show |
1 | a0006c0008t0003g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.512-5329_512-5328i others(409): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690385 | ||||||
chr2:3690385 | C | CCCCTCCC others(119): Show |
1 | a0003c0003t0002g0183 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.512-5329_512-5328i others(128): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690385 | ||||||
chr2:3690385 | C | CCCCTCCC others(109): Show |
1 | a0003c0003t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.512-5329_512-5328i others(118): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690385 | ||||||
chr2:3690385 | C | CCCCTCCC others(124): Show |
1 | a0003c0003t0001g0201 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.512-5329_512-5328i others(133): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690385 | ||||||
chr2:3690385 | C | T | 2 | a0002c0002t0002g0103 a0002c0002t0002g0155 |
2 | HG04228.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.512-5332C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690385 | |||||||
chr2:3690386 | C | CCCCCTCC others(32): Show |
1 | a0001c0001t0001g0002 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.512-5294_512-5293i others(41): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690386 | ||||||
chr2:3690386 | C | CTCCCCCT others(66): Show |
1 | a0002c0014t0002g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.512-5331_512-5330i others(75): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690386 | |||||||
chr2:3690386 | C | T | 2 | a0003c0003t0002g0123 a0004c0004t0001g0037 |
2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.512-5331C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690386 | |||||||
chr2:3690388 | C | T | 1 | a0002c0002t0002g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.512-5329C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690388 | |||||||
chr2:3690389 | C | T | 2 | a0003c0003t0002g0042 a0003c0003t0002g0122 |
2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.512-5328C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690389 | |||||||
chr2:3690390 | C | T | 13 | a0002c0002t0001g0069 a0002c0002t0001g0202 a0002c0002t0002g0019 others(10): Show |
15 | HG01243.hp2 HG01891.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.512-5327C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690390 | |||||||
chr2:3690391 | T | C | 14 | a0002c0002t0001g0069 a0002c0002t0001g0202 a0002c0002t0001g0205 others(11): Show |
16 | HG01243.hp2 HG01891.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.512-5326T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690391 | |||||||
chr2:3690391 | T | TCCCCTCC others(161): Show |
1 | a0002c0002t0002g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.512-5317_512-5316i others(170): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690391 | ||||||
chr2:3690391 | T | TCCCCTCC others(5): Show |
1 | a0002c0005t0001g0206 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.512-5311_512-5300d others(14): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690391 | ||||||
chr2:3690396 | T | C | 1 | a0002c0006t0001g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.512-5321T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690396 | |||||||
chr2:3690396 | T | TC | 5 | a0002c0002t0001g0069 a0002c0002t0002g0019 a0002c0002t0002g0060 others(2): Show |
5 | HG01975.hp2 HG03669.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.512-5317dupC | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690396 | ||||||
chr2:3690396 | T | TCCCCCCT others(185): Show |
1 | a0003c0003t0002g0211 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.512-5317_512-5316i others(194): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690396 | ||||||
chr2:3690396 | T | TCCCCCTC others(27): Show |
6 | a0002c0002t0001g0054 a0002c0002t0002g0004 a0002c0002t0002g0128 others(3): Show |
8 | HG01123.hp1 HG02004.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.512-5317_512-5316i others(36): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690396 | ||||||
chr2:3690396 | T | TCCCCCTC others(77): Show |
1 | a0002c0002t0001g0086 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.512-5317_512-5316i others(86): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690396 | ||||||
chr2:3690396 | T | TCCCCCTC others(82): Show |
1 | a0002c0002t0001g0081 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.512-5317_512-5316i others(91): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690396 | ||||||
chr2:3690396 | T | TCCCCCTC others(76): Show |
12 | a0002c0002t0001g0071 a0002c0002t0001g0080 a0002c0002t0001g0085 others(9): Show |
12 | HG00280.hp2 HG00639.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.512-5317_512-5316i others(85): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690396 | ||||||
chr2:3690396 | T | TCCCCCTC others(114): Show |
2 | a0002c0002t0002g0212 a0002c0002t0002g0213 |
2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.512-5317_512-5316i others(123): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690396 | ||||||
chr2:3690397 | C | CCCCCTCC others(30): Show |
1 | a0002c0002t0002g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.512-5317_512-5316i others(39): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690397 | ||||||
chr2:3690401 | T | C | 3 | a0003c0003t0001g0005 a0003c0003t0001g0053 a0007c0011t0001g0124 |
3 | HG02486.hp1 HG02738.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.512-5316T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690401 | |||||||
chr2:3690402 | C | CCCACTCC others(111): Show |
2 | a0003c0003t0002g0026 a0003c0003t0002g0027 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.512-5313_512-5312i others(120): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCCTCC others(3): Show |
1 | a0003c0003t0002g0016 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.512-5311_512-5310i others(12): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCCTCC others(68): Show |
1 | a0003c0003t0002g0017 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.512-5311_512-5310i others(77): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCCTCC others(83): Show |
1 | a0003c0003t0002g0177 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.512-5311_512-5310i others(92): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCCTCC others(68): Show |
3 | a0003c0003t0002g0171 a0003c0003t0002g0178 a0003c0003t0002g0179 |
3 | HG02056.hp2 HG02523.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.512-5311_512-5310i others(77): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCCTCC others(67): Show |
4 | a0003c0003t0001g0065 a0003c0003t0002g0017 a0003c0003t0002g0136 others(1): Show |
4 | HG00735.hp2 HG01361.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.512-5311_512-5310i others(76): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCCTCC others(67): Show |
2 | a0003c0003t0001g0097 a0003c0003t0002g0172 |
2 | NA19074.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.512-5311_512-5310i others(76): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCCTCC others(66): Show |
1 | a0003c0003t0001g0098 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.512-5311_512-5310i others(75): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCCTCC others(70): Show |
1 | a0003c0003t0002g0043 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.512-5311_512-5310i others(79): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCCTCC others(69): Show |
3 | a0002c0002t0002g0210 a0003c0003t0002g0042 a0003c0003t0002g0122 |
3 | HG02145.hp2 HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.512-5311_512-5310i others(78): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCCTCC others(79): Show |
1 | a0003c0003t0002g0018 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.512-5311_512-5310i others(88): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCCTCC others(65): Show |
1 | a0003c0003t0002g0018 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.512-5311_512-5310i others(74): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCTCCC others(94): Show |
1 | a0002c0002t0002g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.512-5312_512-5311i others(103): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCTCCC others(88): Show |
1 | a0003c0003t0002g0163 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.512-5312_512-5311i others(97): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCTCCC others(110): Show |
1 | a0003c0003t0002g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.512-5312_512-5311i others(119): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCTCCC others(98): Show |
1 | a0002c0013t0002g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.512-5312_512-5311i others(107): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | CCCCTCCC others(123): Show |
1 | a0002c0002t0002g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.512-5312_512-5311i others(132): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690402 | ||||||
chr2:3690402 | C | T | 1 | a0003c0003t0001g0053 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.512-5315C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690402 | |||||||
chr2:3690403 | C | CCCCCTCC others(43): Show |
1 | a0001c0001t0001g0073 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.512-5305_512-5256d others(52): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690403 | ||||||
chr2:3690403 | C | T | 2 | a0002c0002t0002g0149 a0007c0011t0001g0124 |
2 | HG02486.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.512-5314C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690403 | |||||||
chr2:3690407 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.512-5310C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690407 | |||||||
chr2:3690407 | CTCCCCTC others(10): Show |
C | 19 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0002c0002t0002g0062 others(16): Show |
21 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.512-5299_512-5283d others(19): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690407 | ||||||
chr2:3690408 | T | C | 1 | a0005c0007t0004g0225 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.512-5309T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690408 | |||||||
chr2:3690408 | T | TC | 5 | a0002c0002t0001g0205 a0003c0003t0001g0200 a0003c0003t0001g0201 others(2): Show |
5 | HG01081.hp2 HG02071.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.512-5305dupC | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690408 | ||||||
chr2:3690418 | T | C | 3 | a0005c0007t0004g0226 a0005c0007t0004g0229 a0007c0011t0001g0124 |
3 | HG02486.hp1 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.512-5299T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690418 | |||||||
chr2:3690418 | T | TC | 6 | a0001c0001t0001g0001 a0002c0002t0001g0081 a0002c0002t0002g0061 others(3): Show |
6 | HG01515.hp1 HG01975.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.512-5294dupC | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690418 | ||||||
chr2:3690418 | T | TCCCCCTT others(50): Show |
1 | a0001c0001t0002g0195 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.512-5256_512-5255i others(59): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690418 | ||||||
chr2:3690420 | C | CCCTCCCC others(61): Show |
1 | a0001c0001t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.512-5295_512-5294i others(70): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690420 | ||||||
chr2:3690420 | C | T | 3 | a0005c0007t0004g0226 a0005c0007t0004g0229 a0007c0011t0001g0124 |
3 | HG02486.hp1 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.512-5297C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690420 | |||||||
chr2:3690420 | CCCCTTCC others(11): Show |
C | 5 | a0002c0002t0001g0142 a0002c0002t0002g0209 a0002c0009t0002g0023 others(2): Show |
5 | HG02717.hp1 HG02886.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.512-5293_512-5276d others(20): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690420 | ||||||
chr2:3690422 | C | A | 1 | a0004c0004t0001g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.512-5295C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690422 | |||||||
chr2:3690423 | C | T | 2 | a0003c0003t0002g0123 a0005c0007t0004g0225 |
2 | HG01123.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.512-5294C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690423 | |||||||
chr2:3690424 | T | C | 86 | a0001c0001t0001g0040 a0002c0002t0001g0054 a0002c0002t0001g0069 others(83): Show |
94 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.512-5293T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690424 | |||||||
chr2:3690424 | T | TCCCCCCT others(4): Show |
1 | a0002c0002t0002g0149 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.512-5293_512-5292i others(13): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690424 | |||||||
chr2:3690424 | T | TCCCCCTC others(23): Show |
1 | a0002c0002t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.512-5293_512-5292i others(32): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690424 | |||||||
chr2:3690424 | T | TCCCCTCC others(62): Show |
1 | a0002c0002t0002g0155 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.512-5293_512-5292i others(71): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690424 | |||||||
chr2:3690425 | T | C | 3 | a0002c0002t0001g0081 a0002c0002t0002g0134 a0005c0007t0004g0225 |
3 | HG01123.hp2 HG01978.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.512-5292T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690425 | |||||||
chr2:3690426 | C | CCCCTCCC others(32): Show |
1 | a0004c0004t0001g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.512-5283_512-5282i others(41): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690426 | ||||||
chr2:3690430 | T | C | 1 | a0002c0014t0002g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.512-5287T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690430 | |||||||
chr2:3690433 | C | CCTCCCCT others(179): Show |
1 | a0002c0002t0002g0222 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.512-5283_512-5282i others(188): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690433 | ||||||
chr2:3690433 | C | T | 1 | a0002c0014t0002g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.512-5284C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690433 | |||||||
chr2:3690435 | C | A | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0003c0003t0001g0038 others(8): Show |
11 | HG02257.hp1 HG02258.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.512-5282C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690435 | |||||||
chr2:3690435 | C | T | 28 | a0002c0002t0002g0162 a0002c0002t0002g0210 a0002c0002t0002g0214 others(25): Show |
31 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.512-5282C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690435 | |||||||
chr2:3690437 | CT | C | 27 | a0002c0002t0002g0162 a0002c0002t0002g0210 a0002c0002t0002g0214 others(24): Show |
30 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.512-5279delT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690437 | |||||||
chr2:3690438 | T | C | 18 | a0002c0002t0001g0070 a0002c0002t0001g0109 a0002c0002t0002g0003 others(15): Show |
22 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.512-5279T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690438 | |||||||
chr2:3690438 | T | TCCCCTCC others(6): Show |
1 | a0003c0003t0001g0053 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.512-5270_512-5269i others(15): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690438 | ||||||
chr2:3690439 | C | A | 12 | a0002c0005t0001g0206 a0002c0005t0001g0207 a0002c0005t0001g0208 others(9): Show |
12 | HG02055.hp1 HG02451.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.512-5278C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690439 | |||||||
chr2:3690443 | T | TCCCCCCC others(8): Show |
1 | a0002c0002t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.512-5270_512-5269i others(17): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690443 | ||||||
chr2:3690558 | G | T | 3 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.512-5159G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690558 | |||||||
chr2:3690612 | T | A | 1 | a0003c0003t0002g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.512-5105T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690612 | |||||||
chr2:3690652 | A | T | 1 | a0002c0002t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.512-5065A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690652 | |||||||
chr2:3690667 | A | G | 1 | a0002c0002t0001g0081 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.512-5050A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690667 | |||||||
chr2:3690668 | G | A | 1 | a0002c0002t0001g0081 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.512-5049G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690668 | |||||||
chr2:3690674 | C | A | 1 | a0002c0002t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.512-5043C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690674 | |||||||
chr2:3690674 | C | CA | 37 | a0001c0001t0001g0072 a0001c0001t0001g0078 a0001c0001t0001g0129 others(34): Show |
41 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.512-5034dupA | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690674 | ||||||
chr2:3690824 | G | T | 1 | a0002c0002t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.512-4893G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690824 | |||||||
chr2:3690869 | G | A | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.512-4848G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690869 | |||||||
chr2:3690875 | G | A | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.512-4842G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3690875 | |||||||
chr2:3690954 | G | GT | 42 | a0001c0001t0001g0093 a0002c0002t0001g0142 a0002c0002t0002g0209 others(39): Show |
45 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.512-4751dupT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690954 | ||||||
chr2:3690954 | GT | G | 66 | a0001c0001t0001g0088 a0001c0001t0001g0130 a0002c0002t0001g0054 others(63): Show |
78 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.512-4751delT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3690954 | ||||||
chr2:3691254 | CT | C | 7 | a0001c0001t0001g0074 a0001c0001t0001g0143 a0002c0002t0002g0133 others(4): Show |
7 | HG01168.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.512-4450delT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3691254 | ||||||
chr2:3691345 | TTTGGCTC others(6): Show |
T | 1 | a0001c0001t0001g0072 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.512-4369_512-4357d others(15): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 3691345 | ||||||
chr2:3691429 | T | G | 2 | a0006c0008t0002g0181 a0006c0008t0003g0231 |
2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.512-4288T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3691429 | |||||||
chr2:3691439 | T | A | 80 | a0002c0002t0001g0054 a0002c0002t0001g0069 a0002c0002t0001g0070 others(77): Show |
92 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.512-4278T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3691439 | |||||||
chr2:3691494 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.512-4223C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3691494 | |||||||
chr2:3691556 | C | T | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.512-4161C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3691556 | |||||||
chr2:3691651 | T | G | 81 | a0001c0001t0001g0040 a0002c0002t0001g0054 a0002c0002t0001g0069 others(78): Show |
93 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.512-4066T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3691651 | |||||||
chr2:3691774 | A | T | 121 | a0001c0001t0001g0040 a0002c0002t0001g0054 a0002c0002t0001g0069 others(118): Show |
136 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.512-3943A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3691774 | |||||||
chr2:3691906 | T | G | 36 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(33): Show |
39 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.512-3811T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3691906 | |||||||
chr2:3691925 | C | T | 3 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0014t0002g0218 |
3 | HG02809.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.512-3792C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3691925 | |||||||
chr2:3691995 | A | G | 1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.512-3722A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3691995 | |||||||
chr2:3691999 | C | G | 3 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0014t0002g0218 |
3 | HG02809.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.512-3718C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3691999 | |||||||
chr2:3692188 | T | C | 15 | a0002c0002t0001g0070 a0002c0002t0001g0109 a0002c0002t0002g0003 others(12): Show |
19 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.512-3529T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3692188 | |||||||
chr2:3692240 | T | A | 1 | a0004c0004t0002g0180 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.512-3477T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3692240 | |||||||
chr2:3692383 | A | T | 1 | a0003c0003t0002g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.512-3334A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3692383 | |||||||
chr2:3692597 | A | C | 1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.512-3120A>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3692597 | |||||||
chr2:3692785 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.512-2932G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3692785 | |||||||
chr2:3692853 | T | G | 1 | a0001c0001t0001g0199 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.512-2864T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3692853 | |||||||
chr2:3692886 | C | G | 27 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(24): Show |
30 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.512-2831C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3692886 | |||||||
chr2:3692955 | A | G | 3 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0014t0002g0218 |
3 | HG02809.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.512-2762A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3692955 | |||||||
chr2:3692963 | A | G | 1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.512-2754A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3692963 | |||||||
chr2:3693067 | C | A | 40 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(37): Show |
43 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.512-2650C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693067 | |||||||
chr2:3693125 | G | A | 40 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(37): Show |
43 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.512-2592G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693125 | |||||||
chr2:3693269 | G | A | 13 | a0002c0005t0001g0206 a0002c0005t0001g0207 a0002c0005t0001g0208 others(10): Show |
13 | HG02055.hp1 HG02451.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.512-2448G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693269 | |||||||
chr2:3693297 | T | A | 1 | a0003c0003t0002g0159 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.512-2420T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693297 | |||||||
chr2:3693345 | A | G | 6 | a0003c0003t0002g0006 a0003c0003t0002g0015 a0003c0003t0002g0032 others(3): Show |
8 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.512-2372A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693345 | |||||||
chr2:3693507 | G | T | 3 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.512-2210G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693507 | |||||||
chr2:3693804 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.512-1913A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693804 | |||||||
chr2:3693813 | C | A | 1 | a0002c0014t0002g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.512-1904C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693813 | |||||||
chr2:3693825 | T | C | 15 | a0002c0002t0001g0070 a0002c0002t0001g0109 a0002c0002t0002g0003 others(12): Show |
19 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.512-1892T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693825 | |||||||
chr2:3693913 | G | A | 1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.512-1804G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693913 | |||||||
chr2:3693936 | C | T | 42 | a0002c0002t0001g0054 a0002c0002t0001g0069 a0002c0002t0001g0071 others(39): Show |
48 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.512-1781C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693936 | |||||||
chr2:3693989 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.512-1728A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693989 | |||||||
chr2:3693994 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.512-1723G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693994 | |||||||
chr2:3693995 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.512-1722A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3693995 | |||||||
chr2:3694112 | A | G | 1 | a0004c0004t0002g0173 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.512-1605A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3694112 | |||||||
chr2:3694546 | C | T | 1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.512-1171C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3694546 | |||||||
chr2:3694566 | G | A | 42 | a0002c0002t0001g0054 a0002c0002t0001g0069 a0002c0002t0001g0071 others(39): Show |
48 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.512-1151G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3694566 | |||||||
chr2:3694881 | C | T | 13 | a0002c0005t0001g0206 a0002c0005t0001g0207 a0002c0005t0001g0208 others(10): Show |
13 | HG02055.hp1 HG02451.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.512-836C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3694881 | |||||||
chr2:3694899 | G | A | 1 | a0004c0004t0002g0173 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.512-818G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3694899 | |||||||
chr2:3695119 | C | T | 1 | a0004c0004t0003g0224 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.512-598C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3695119 | |||||||
chr2:3695232 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.512-485C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 7/11 | chr2 | 3695232 | |||||||
chr2:3696561 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0184 |
3 | NA18979.hp2 NA18999.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.741+213C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3696561 | |||||||
chr2:3696638 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.741+290T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3696638 | |||||||
chr2:3696748 | G | A | 13 | a0002c0005t0001g0206 a0002c0005t0001g0207 a0002c0005t0001g0208 others(10): Show |
13 | HG02055.hp1 HG02451.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.741+400G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3696748 | |||||||
chr2:3696767 | T | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0089 a0001c0001t0001g0093 others(1): Show |
5 | HG01192.hp1 HG01358.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.741+419T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3696767 | |||||||
chr2:3696940 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.742-408T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3696940 | |||||||
chr2:3696988 | G | A | 1 | a0003c0003t0002g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.742-360G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3696988 | |||||||
chr2:3697023 | A | G | 1 | a0001c0001t0003g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.742-325A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3697023 | |||||||
chr2:3697055 | A | T | 125 | a0001c0001t0001g0040 a0002c0002t0001g0054 a0002c0002t0001g0069 others(122): Show |
140 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.742-293A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3697055 | |||||||
chr2:3697060 | C | T | 1 | a0004c0004t0002g0173 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.742-288C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3697060 | |||||||
chr2:3697138 | A | G | 84 | a0002c0002t0001g0054 a0002c0002t0001g0069 a0002c0002t0001g0070 others(81): Show |
96 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.742-210A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3697138 | |||||||
chr2:3697230 | C | G | 3 | a0003c0003t0002g0168 a0003c0003t0002g0169 a0003c0003t0002g0176 |
3 | NA19007.hp2 NA19054.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.742-118C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3697230 | |||||||
chr2:3697245 | A | T | 7 | a0002c0002t0002g0024 a0003c0003t0002g0006 a0003c0003t0002g0015 others(4): Show |
9 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.742-103A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3697245 | |||||||
chr2:3697260 | G | A | 6 | a0003c0003t0002g0006 a0003c0003t0002g0015 a0003c0003t0002g0032 others(3): Show |
8 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.742-88G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3697260 | |||||||
chr2:3697266 | C | T | 1 | a0003c0003t0002g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.742-82C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 9/11 | chr2 | 3697266 | |||||||
chr2:3697609 | C | CTCTG | 11 | a0001c0001t0001g0125 a0001c0001t0001g0166 a0001c0001t0002g0145 others(8): Show |
11 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.850+165_850+168dup others(4): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697609 | ||||||
chr2:3697609 | C | CTCTGTCT others(1): Show |
3 | a0003c0003t0002g0028 a0003c0003t0002g0158 a0003c0003t0002g0211 |
3 | HG02055.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.850+161_850+168dup others(8): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697609 | ||||||
chr2:3697609 | C | CTCTGTCT others(5): Show |
3 | a0002c0005t0001g0208 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG02559.hp2 HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.850+157_850+168dup others(12): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697609 | ||||||
chr2:3697609 | CTCTG | C | 25 | a0001c0001t0001g0050 a0002c0002t0001g0069 a0002c0002t0001g0085 others(22): Show |
30 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.850+165_850+168del others(4): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697609 | ||||||
chr2:3697617 | GTCTGTCT others(1): Show |
G | 19 | a0002c0002t0001g0070 a0002c0002t0001g0071 a0002c0002t0001g0095 others(16): Show |
23 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.850+165_850+172del others(8): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697617 | ||||||
chr2:3697617 | GTCTGTCT others(5): Show |
G | 1 | a0002c0002t0002g0139 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.850+165_850+176del others(12): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697617 | ||||||
chr2:3697621 | G | A | 16 | a0001c0001t0002g0196 a0002c0002t0001g0054 a0002c0002t0001g0080 others(13): Show |
17 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.850+165G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3697621 | |||||||
chr2:3697621 | G | GTCTA | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(18): Show |
28 | HG00544.hp2 HG00735.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.850+209_850+212dup others(4): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697621 | ||||||
chr2:3697621 | G | GTCTATCT others(1): Show |
11 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00423.hp2 HG00558.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.850+205_850+212dup others(8): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697621 | ||||||
chr2:3697621 | G | GTCTGTCT others(1): Show |
12 | a0001c0001t0001g0044 a0001c0001t0001g0126 a0001c0001t0001g0129 others(9): Show |
12 | HG02055.hp2 HG02056.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.850+168_850+169ins others(8): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697621 | ||||||
chr2:3697621 | G | GTCTGTCT others(5): Show |
4 | a0002c0009t0002g0023 a0003c0003t0002g0026 a0003c0003t0002g0027 others(1): Show |
4 | HG02258.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+168_850+169ins others(12): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697621 | ||||||
chr2:3697621 | G | GTCTGTCT others(9): Show |
5 | a0001c0001t0001g0025 a0001c0001t0001g0131 a0001c0001t0001g0233 others(2): Show |
5 | HG01884.hp1 HG01884.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+168_850+169ins others(16): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697621 | ||||||
chr2:3697621 | G | GTCTGTCT others(5): Show |
4 | a0002c0005t0001g0206 a0002c0005t0001g0215 a0002c0005t0002g0022 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+168_850+169ins others(12): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697621 | ||||||
chr2:3697621 | G | GTCTGTCT others(9): Show |
1 | a0003c0003t0002g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.850+168_850+169ins others(16): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697621 | ||||||
chr2:3697621 | G | GTCTGTCT others(13): Show |
1 | a0003c0003t0002g0048 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.850+168_850+169ins others(20): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697621 | ||||||
chr2:3697621 | G | GTCTGTCT others(9): Show |
3 | a0002c0002t0002g0133 a0002c0005t0002g0047 a0005c0007t0004g0225 |
3 | HG01123.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.850+168_850+169ins others(16): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697621 | ||||||
chr2:3697621 | G | GTCTGTCT others(13): Show |
2 | a0002c0002t0002g0134 a0002c0014t0002g0218 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.850+168_850+169ins others(20): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697621 | ||||||
chr2:3697621 | G | GTCTGTCT others(17): Show |
1 | a0002c0005t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.850+168_850+169ins others(24): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697621 | ||||||
chr2:3697621 | GTCTA | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(41): Show |
51 | HG00423.hp1 HG00558.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.850+209_850+212del others(4): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697621 | ||||||
chr2:3697621 | GTCTATCT others(5): Show |
G | 2 | a0001c0001t0001g0040 a0003c0003t0002g0221 |
2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.850+201_850+212del others(12): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3697621 | ||||||
chr2:3697625 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0166 a0003c0003t0001g0053 others(8): Show |
11 | HG02083.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.850+169A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3697625 | |||||||
chr2:3697629 | A | G | 19 | a0001c0001t0005g0090 a0002c0002t0001g0142 a0002c0002t0002g0162 others(16): Show |
22 | HG00423.hp1 HG00735.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.850+173A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3697629 | |||||||
chr2:3697637 | A | G | 1 | a0003c0003t0002g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.850+181A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3697637 | |||||||
chr2:3697711 | C | G | 125 | a0001c0001t0001g0040 a0002c0002t0001g0054 a0002c0002t0001g0069 others(122): Show |
140 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.850+255C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3697711 | |||||||
chr2:3697930 | G | T | 3 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.850+474G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3697930 | |||||||
chr2:3697946 | T | C | 6 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0002g0128 others(3): Show |
6 | HG01109.hp1 HG01123.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+490T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3697946 | |||||||
chr2:3697960 | C | T | 3 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.850+504C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3697960 | |||||||
chr2:3698207 | C | T | 1 | a0002c0002t0002g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.850+751C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3698207 | |||||||
chr2:3698252 | C | T | 1 | a0002c0013t0002g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.850+796C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3698252 | |||||||
chr2:3698308 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.850+852C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3698308 | |||||||
chr2:3698377 | C | T | 38 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(35): Show |
41 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.850+921C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3698377 | |||||||
chr2:3698456 | C | G | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.850+1000C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3698456 | |||||||
chr2:3698619 | C | T | 27 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(24): Show |
30 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.850+1163C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3698619 | |||||||
chr2:3698778 | ATACTTT | A | 15 | a0002c0002t0001g0070 a0002c0002t0001g0109 a0002c0002t0002g0003 others(12): Show |
19 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.850+1323_850+1328d others(8): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3698778 | |||||||
chr2:3698782 | T | TTTAAGTT others(79): Show |
1 | a0001c0001t0001g0091 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.850+1373_850+1374i others(88): Show |
ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3698782 | ||||||
chr2:3698943 | A | G | 1 | a0003c0003t0002g0183 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.850+1487A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3698943 | |||||||
chr2:3699009 | C | T | 1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.850+1553C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3699009 | |||||||
chr2:3699022 | G | GT | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0003c0003t0001g0038 others(7): Show |
10 | HG02257.hp1 HG02258.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.850+1572dupT | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 3699022 | ||||||
chr2:3699026 | T | G | 3 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 |
3 | HG01123.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.850+1570T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3699026 | |||||||
chr2:3699070 | T | A | 1 | a0002c0002t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.850+1614T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3699070 | |||||||
chr2:3699072 | G | T | 1 | a0002c0002t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.850+1616G>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3699072 | |||||||
chr2:3699073 | T | G | 1 | a0002c0002t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.850+1617T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3699073 | |||||||
chr2:3699077 | A | G | 45 | a0002c0002t0001g0054 a0002c0002t0001g0069 a0002c0002t0001g0071 others(42): Show |
51 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.850+1621A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3699077 | |||||||
chr2:3699170 | C | T | 37 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(34): Show |
40 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.850+1714C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3699170 | |||||||
chr2:3699431 | T | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0094 a0001c0001t0001g0113 |
3 | HG00642.hp2 HG01192.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.850+1975T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3699431 | |||||||
chr2:3699609 | A | G | 1 | a0003c0003t0002g0014 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.851-1903A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3699609 | |||||||
chr2:3699647 | C | G | 38 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(35): Show |
41 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.851-1865C>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3699647 | |||||||
chr2:3699816 | T | G | 1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.851-1696T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3699816 | |||||||
chr2:3700010 | A | C | 1 | a0002c0002t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.851-1502A>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3700010 | |||||||
chr2:3700011 | T | A | 1 | a0002c0002t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.851-1501T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3700011 | |||||||
chr2:3700066 | C | A | 25 | a0002c0002t0002g0162 a0002c0002t0002g0210 a0002c0002t0002g0214 others(22): Show |
28 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.851-1446C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3700066 | |||||||
chr2:3700256 | T | G | 41 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(38): Show |
44 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.851-1256T>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3700256 | |||||||
chr2:3700330 | A | G | 3 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0014t0002g0218 |
3 | HG02809.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.851-1182A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3700330 | |||||||
chr2:3700490 | A | G | 1 | a0003c0003t0002g0183 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.851-1022A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3700490 | |||||||
chr2:3700688 | T | C | 41 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(38): Show |
44 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.851-824T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3700688 | |||||||
chr2:3700790 | G | A | 1 | a0003c0003t0002g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.851-722G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3700790 | |||||||
chr2:3700831 | T | A | 1 | a0002c0002t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.851-681T>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3700831 | |||||||
chr2:3700853 | G | C | 5 | a0005c0007t0004g0225 a0005c0007t0004g0226 a0005c0007t0004g0229 others(2): Show |
5 | HG01123.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.851-659G>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3700853 | |||||||
chr2:3701321 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.851-191C>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3701321 | |||||||
chr2:3701348 | G | A | 12 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0129 others(9): Show |
12 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.851-164G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3701348 | |||||||
chr2:3701381 | T | C | 40 | a0002c0002t0001g0142 a0002c0002t0002g0162 a0002c0002t0002g0209 others(37): Show |
43 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.851-131T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3701381 | |||||||
chr2:3701480 | G | A | 1 | a0001c0001t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.851-32G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3701480 | |||||||
chr2:3701494 | T | C | 83 | a0002c0002t0001g0054 a0002c0002t0001g0069 a0002c0002t0001g0070 others(80): Show |
95 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.851-18T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 10/11 | chr2 | 3701494 | |||||||
chr2:3701662 | C | T | 1 | a0007c0011t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.975+26C>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 11/11 | chr2 | 3701662 | |||||||
chr2:3701677 | G | A | 85 | a0002c0002t0001g0054 a0002c0002t0001g0069 a0002c0002t0001g0070 others(82): Show |
97 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.975+41G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 11/11 | chr2 | 3701677 | |||||||
chr2:3701848 | A | G | 118 | a0002c0002t0001g0054 a0002c0002t0001g0069 a0002c0002t0001g0070 others(115): Show |
133 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.975+212A>G | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 11/11 | chr2 | 3701848 | |||||||
chr2:3701870 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.975+234A>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 11/11 | chr2 | 3701870 | |||||||
chr2:3701936 | G | A | 3 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0014t0002g0218 |
3 | HG02809.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.975+300G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 11/11 | chr2 | 3701936 | |||||||
chr2:3701956 | T | C | 134 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0002c0002t0001g0054 others(131): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.975+320T>C | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 11/11 | chr2 | 3701956 | |||||||
chr2:3702139 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.976-224G>A | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 11/11 | chr2 | 3702139 | |||||||
chr2:3702151 | A | T | 15 | a0002c0002t0001g0070 a0002c0002t0001g0109 a0002c0002t0002g0003 others(12): Show |
19 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.976-212A>T | ALLC | ENSG00000151360.10 | transcript | ENST00000252505.4 | protein_coding | 11/11 | chr2 | 3702151 |