Item | Value |
---|---|
geneid | 26524 |
ensemblid | ENSG00000150457.9 |
hgncid | 6515 |
symbol | LATS2 |
name | large tumor suppressor kinase 2 |
refseq_nuc | NM_014572.3 |
refseq_prot | NP_055387.2 |
ensembl_nuc | ENST00000382592.5 |
ensembl_prot | ENSP00000372035.4 |
mane_status | MANE Select |
chr | chr13 |
start | 20973036 |
end | 21061586 |
strand | - |
ver | v1.2 |
region | chr13:20973036-21061586 |
region5000 | chr13:20968036-21066586 |
regionname0 | LATS2_chr13_20973036_21061586 |
regionname5000 | LATS2_chr13_20968036_21066586 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1090 | 101 | 10 | 24 | 53 | 4 | 9 | 42 | LATS2_chr13_20968036_21066586 | LATS2 | MRPKT others(1085): Show |
chr13 | 20968036 | 21066586 |
a0002 | 0/0 | 1088 | 83 | 12 | 17 | 48 | 1 | 5 | 38 | LATS2_chr13_20968036_21066586 | LATS2 | MRPKT others(1083): Show |
chr13 | 20968036 | 21066586 |
a0003 | 0/0 | 1088 | 78 | 32 | 14 | 22 | 1 | 9 | 17 | LATS2_chr13_20968036_21066586 | LATS2 | MRPKT others(1083): Show |
chr13 | 20968036 | 21066586 |
a0004 | 1/0 | 1088 | 34 | 15 | 6 | 0 | 4 | 8 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | MRPKT others(1083): Show |
chr13 | 20968036 | 21066586 |
a0005 | 0/0 | 1090 | 7 | 5 | 1 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | MRPKT others(1085): Show |
chr13 | 20968036 | 21066586 |
a0006 | 0/0 | 1088 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | LATS2_chr13_20968036_21066586 | LATS2 | MRPKT others(1083): Show |
chr13 | 20968036 | 21066586 |
a0007 | 0/0 | 1088 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | MRPKT others(1083): Show |
chr13 | 20968036 | 21066586 |
a0008 | 0/0 | 1088 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | MRPKT others(1083): Show |
chr13 | 20968036 | 21066586 |
a0009 | 0/0 | 1090 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | MRPKT others(1085): Show |
chr13 | 20968036 | 21066586 |
a0010 | 0/0 | 1092 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | MRPKT others(1087): Show |
chr13 | 20968036 | 21066586 |
a0011 | 0/0 | 1088 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | MRPKT others(1083): Show |
chr13 | 20968036 | 21066586 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3270 | 88 | 4 | 22 | 49 | 4 | 8 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3265): Show |
chr13 | 20968036 | 21066586 | ||
a0001c0010 | 0/0 | 3270 | 5 | 0 | 1 | 3 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3265): Show |
chr13 | 20968036 | 21066586 | ||
a0001c0011 | 0/0 | 3270 | 5 | 5 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3265): Show |
chr13 | 20968036 | 21066586 | ||
a0001c0022 | 0/0 | 3270 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3265): Show |
chr13 | 20968036 | 21066586 | ||
a0001c0030 | 0/0 | 3270 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3265): Show |
chr13 | 20968036 | 21066586 | ||
a0001c0031 | 0/0 | 3270 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3265): Show |
chr13 | 20968036 | 21066586 | ||
a0002c0002 | 0/0 | 3264 | 60 | 5 | 13 | 37 | 0 | 5 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0002c0006 | 0/0 | 3264 | 14 | 1 | 3 | 9 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0002c0014 | 0/0 | 3264 | 3 | 3 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0002c0017 | 0/0 | 3264 | 2 | 1 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0002c0024 | 0/0 | 3264 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0002c0027 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0002c0028 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0002c0034 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0003c0003 | 0/0 | 3264 | 30 | 6 | 7 | 11 | 0 | 6 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0003c0005 | 0/0 | 3264 | 26 | 7 | 4 | 11 | 1 | 3 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0003c0007 | 0/0 | 3264 | 7 | 7 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0003c0008 | 0/0 | 3264 | 6 | 4 | 2 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0003c0009 | 0/0 | 3264 | 6 | 6 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0003c0023 | 0/0 | 3264 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0003c0032 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0003c0036 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0004c0004 | 0/0 | 3264 | 28 | 11 | 5 | 0 | 4 | 8 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0004c0015 | 1/0 | 3264 | 3 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0004c0019 | 0/0 | 3264 | 2 | 1 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0004c0035 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0005c0012 | 0/0 | 3270 | 4 | 3 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3265): Show |
chr13 | 20968036 | 21066586 | ||
a0005c0016 | 0/0 | 3270 | 3 | 2 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3265): Show |
chr13 | 20968036 | 21066586 | ||
a0006c0013 | 0/0 | 3264 | 4 | 0 | 0 | 4 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0006c0021 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0007c0020 | 0/0 | 3264 | 2 | 0 | 2 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0008c0018 | 0/0 | 3264 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 | ||
a0009c0026 | 0/0 | 3270 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3265): Show |
chr13 | 20968036 | 21066586 | ||
a0009c0033 | 0/0 | 3270 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3265): Show |
chr13 | 20968036 | 21066586 | ||
a0010c0029 | 0/0 | 3276 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3271): Show |
chr13 | 20968036 | 21066586 | ||
a0011c0025 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | ATGAG others(3259): Show |
chr13 | 20968036 | 21066586 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5550 | 52 | 4 | 18 | 21 | 2 | 6 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5545): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0002 | 0/0 | 5549 | 9 | 0 | 3 | 5 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5544): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0003 | 0/0 | 5559 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5554): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0004 | 0/0 | 5552 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5547): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0006 | 0/0 | 5560 | 6 | 0 | 0 | 6 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5555): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0010 | 0/0 | 5551 | 4 | 0 | 0 | 3 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5546): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0012 | 0/0 | 5558 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5553): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0013 | 0/0 | 5548 | 4 | 0 | 0 | 4 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5543): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0017 | 0/0 | 5550 | 2 | 0 | 0 | 2 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5545): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0022 | 0/0 | 5550 | 2 | 0 | 0 | 2 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5545): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0027 | 0/0 | 5549 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5544): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0029 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5555): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0034 | 0/0 | 5550 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5545): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0037 | 0/0 | 5550 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5545): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0043 | 0/0 | 5549 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5544): Show |
chr13 | 20968036 | 21066586 |
a0001c0001t0047 | 0/0 | 5551 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5546): Show |
chr13 | 20968036 | 21066586 |
a0001c0010t0001 | 0/0 | 5550 | 4 | 0 | 1 | 2 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5545): Show |
chr13 | 20968036 | 21066586 |
a0001c0010t0015 | 0/0 | 5551 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5546): Show |
chr13 | 20968036 | 21066586 |
a0001c0011t0001 | 0/0 | 5550 | 5 | 5 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5545): Show |
chr13 | 20968036 | 21066586 |
a0001c0022t0004 | 0/0 | 5552 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5547): Show |
chr13 | 20968036 | 21066586 |
a0001c0030t0001 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5545): Show |
chr13 | 20968036 | 21066586 |
a0001c0031t0006 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5555): Show |
chr13 | 20968036 | 21066586 |
a0002c0002t0003 | 0/0 | 5553 | 44 | 0 | 11 | 29 | 0 | 4 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5548): Show |
chr13 | 20968036 | 21066586 |
a0002c0002t0006 | 0/0 | 5554 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5549): Show |
chr13 | 20968036 | 21066586 |
a0002c0002t0007 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5539): Show |
chr13 | 20968036 | 21066586 |
a0002c0002t0010 | 0/0 | 5545 | 2 | 1 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5540): Show |
chr13 | 20968036 | 21066586 |
a0002c0002t0011 | 0/0 | 5552 | 4 | 3 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5547): Show |
chr13 | 20968036 | 21066586 |
a0002c0002t0012 | 0/0 | 5552 | 3 | 0 | 0 | 3 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5547): Show |
chr13 | 20968036 | 21066586 |
a0002c0002t0023 | 0/0 | 5551 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5546): Show |
chr13 | 20968036 | 21066586 |
a0002c0002t0024 | 0/0 | 5552 | 2 | 0 | 0 | 2 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5547): Show |
chr13 | 20968036 | 21066586 |
a0002c0002t0040 | 0/0 | 5555 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5550): Show |
chr13 | 20968036 | 21066586 |
a0002c0002t0042 | 0/0 | 5553 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5548): Show |
chr13 | 20968036 | 21066586 |
a0002c0006t0004 | 0/0 | 5546 | 14 | 1 | 3 | 9 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0002c0014t0018 | 0/0 | 5547 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5542): Show |
chr13 | 20968036 | 21066586 |
a0002c0014t0038 | 0/0 | 5553 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5548): Show |
chr13 | 20968036 | 21066586 |
a0002c0017t0006 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5549): Show |
chr13 | 20968036 | 21066586 |
a0002c0017t0011 | 0/0 | 5552 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5547): Show |
chr13 | 20968036 | 21066586 |
a0002c0024t0023 | 0/0 | 5551 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5546): Show |
chr13 | 20968036 | 21066586 |
a0002c0027t0039 | 0/0 | 5553 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5548): Show |
chr13 | 20968036 | 21066586 |
a0002c0028t0041 | 0/0 | 5547 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5542): Show |
chr13 | 20968036 | 21066586 |
a0002c0034t0035 | 0/0 | 5553 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5548): Show |
chr13 | 20968036 | 21066586 |
a0003c0003t0001 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5539): Show |
chr13 | 20968036 | 21066586 |
a0003c0003t0002 | 0/0 | 5543 | 16 | 2 | 6 | 4 | 0 | 4 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5538): Show |
chr13 | 20968036 | 21066586 |
a0003c0003t0004 | 0/0 | 5546 | 3 | 3 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0003c0003t0007 | 0/0 | 5544 | 7 | 0 | 1 | 5 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5539): Show |
chr13 | 20968036 | 21066586 |
a0003c0003t0017 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5539): Show |
chr13 | 20968036 | 21066586 |
a0003c0003t0025 | 0/0 | 5548 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5543): Show |
chr13 | 20968036 | 21066586 |
a0003c0003t0044 | 0/0 | 5546 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0003c0005t0001 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5539): Show |
chr13 | 20968036 | 21066586 |
a0003c0005t0002 | 0/0 | 5543 | 20 | 5 | 3 | 8 | 1 | 3 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5538): Show |
chr13 | 20968036 | 21066586 |
a0003c0005t0004 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0003c0005t0012 | 0/0 | 5552 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5547): Show |
chr13 | 20968036 | 21066586 |
a0003c0005t0015 | 0/0 | 5545 | 2 | 0 | 0 | 2 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5540): Show |
chr13 | 20968036 | 21066586 |
a0003c0005t0033 | 0/0 | 5546 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0003c0007t0008 | 0/0 | 5546 | 5 | 5 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0003c0007t0016 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5539): Show |
chr13 | 20968036 | 21066586 |
a0003c0007t0036 | 0/0 | 5547 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5542): Show |
chr13 | 20968036 | 21066586 |
a0003c0008t0008 | 0/0 | 5546 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0003c0008t0009 | 0/0 | 5545 | 3 | 1 | 2 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5540): Show |
chr13 | 20968036 | 21066586 |
a0003c0008t0046 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0003c0009t0008 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0003c0009t0009 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5540): Show |
chr13 | 20968036 | 21066586 |
a0003c0009t0016 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5539): Show |
chr13 | 20968036 | 21066586 |
a0003c0009t0026 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0003c0009t0031 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0003c0009t0032 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5539): Show |
chr13 | 20968036 | 21066586 |
a0003c0023t0002 | 0/0 | 5543 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5538): Show |
chr13 | 20968036 | 21066586 |
a0003c0032t0016 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5539): Show |
chr13 | 20968036 | 21066586 |
a0003c0036t0009 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5540): Show |
chr13 | 20968036 | 21066586 |
a0004c0004t0001 | 0/0 | 5544 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5539): Show |
chr13 | 20968036 | 21066586 |
a0004c0004t0004 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0004c0004t0005 | 0/0 | 5547 | 16 | 3 | 5 | 0 | 3 | 5 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5542): Show |
chr13 | 20968036 | 21066586 |
a0004c0004t0014 | 0/0 | 5549 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5544): Show |
chr13 | 20968036 | 21066586 |
a0004c0004t0019 | 0/0 | 5550 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5545): Show |
chr13 | 20968036 | 21066586 |
a0004c0004t0021 | 0/0 | 5546 | 2 | 0 | 0 | 0 | 0 | 2 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0004c0004t0025 | 0/0 | 5548 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5543): Show |
chr13 | 20968036 | 21066586 |
a0004c0004t0028 | 0/0 | 5549 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5544): Show |
chr13 | 20968036 | 21066586 |
a0004c0004t0030 | 0/0 | 5550 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5545): Show |
chr13 | 20968036 | 21066586 |
a0004c0004t0045 | 0/0 | 5547 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5542): Show |
chr13 | 20968036 | 21066586 |
a0004c0015t0004 | 1/0 | 5546 | 1 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5541): Show |
chr13 | 20968036 | 21066586 |
a0004c0015t0005 | 0/0 | 5547 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5542): Show |
chr13 | 20968036 | 21066586 |
a0004c0015t0018 | 0/0 | 5547 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5542): Show |
chr13 | 20968036 | 21066586 |
a0004c0019t0020 | 0/0 | 5548 | 2 | 1 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5543): Show |
chr13 | 20968036 | 21066586 |
a0004c0035t0009 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5540): Show |
chr13 | 20968036 | 21066586 |
a0005c0012t0001 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5545): Show |
chr13 | 20968036 | 21066586 |
a0005c0012t0002 | 0/0 | 5549 | 3 | 3 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5544): Show |
chr13 | 20968036 | 21066586 |
a0005c0016t0005 | 0/0 | 5553 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5548): Show |
chr13 | 20968036 | 21066586 |
a0005c0016t0014 | 0/0 | 5555 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5550): Show |
chr13 | 20968036 | 21066586 |
a0006c0013t0002 | 0/0 | 5543 | 3 | 0 | 0 | 3 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5538): Show |
chr13 | 20968036 | 21066586 |
a0006c0013t0007 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5539): Show |
chr13 | 20968036 | 21066586 |
a0006c0021t0002 | 0/0 | 5543 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5538): Show |
chr13 | 20968036 | 21066586 |
a0007c0020t0009 | 0/0 | 5545 | 2 | 0 | 2 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5540): Show |
chr13 | 20968036 | 21066586 |
a0008c0018t0010 | 0/0 | 5545 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5540): Show |
chr13 | 20968036 | 21066586 |
a0009c0026t0011 | 0/0 | 5558 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5553): Show |
chr13 | 20968036 | 21066586 |
a0009c0033t0001 | 0/0 | 5550 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5545): Show |
chr13 | 20968036 | 21066586 |
a0010c0029t0001 | 0/0 | 5556 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5551): Show |
chr13 | 20968036 | 21066586 |
a0011c0025t0003 | 0/0 | 5553 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | GACGC others(5548): Show |
chr13 | 20968036 | 21066586 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0010g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0010g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0010g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0010g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0012g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0013g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0013g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0013g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0013g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0017g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0017g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0022g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0022g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0027g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0029g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0034g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0037g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0043g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0001t0047g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0010t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0010t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0010t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0010t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0010t0015g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0011t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0011t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0011t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0011t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0022t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0030t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0001c0031t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0006g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0010g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0011g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0011g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0011g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0011g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0012g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0012g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0012g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0023g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0024g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0024g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0040g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0002t0042g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0006t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0014t0018g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0014t0018g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0014t0038g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0017t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0017t0011g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0024t0023g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0027t0039g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0028t0041g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0002c0034t0035g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0007g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0007g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0007g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0007g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0007g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0017g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0025g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0003t0044g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0012g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0015g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0015g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0005t0033g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0007t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0007t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0007t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0007t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0007t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0007t0016g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0007t0036g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0008t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0008t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0008t0009g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0008t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0008t0009g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0008t0046g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0009t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0009t0009g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0009t0016g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0009t0026g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0009t0031g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0009t0032g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0023t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0032t0016g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0003c0036t0009g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0005g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0014g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0019g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0019g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0021g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0021g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0025g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0028g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0030g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0004t0045g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0015t0004g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0015t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0015t0018g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0019t0020g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0019t0020g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0004c0035t0009g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0005c0012t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0005c0012t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0005c0012t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0005c0012t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0005c0016t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0005c0016t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0005c0016t0014g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0006c0013t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0006c0013t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0006c0013t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0006c0013t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0006c0021t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0007c0020t0009g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0008c0018t0010g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0008c0018t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0009c0026t0011g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0009c0033t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0010c0029t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
a0011c0025t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00099 | hp2 | a0004 | c0004 | t0005 | g0004 | EUR | GBR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00280 | hp1 | a0001 | c0001 | t0037 | g0186 | EUR | FIN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00280 | hp2 | a0002 | c0006 | t0004 | g0254 | EUR | FIN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00423 | hp1 | a0001 | c0001 | t0006 | g0232 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00438 | hp1 | a0001 | c0001 | t0022 | g0174 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00438 | hp2 | a0002 | c0002 | t0003 | g0142 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00597 | hp2 | a0002 | c0006 | t0004 | g0208 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00621 | hp1 | a0002 | c0002 | t0003 | g0160 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00621 | hp2 | a0003 | c0005 | t0002 | g0063 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00639 | hp1 | a0002 | c0024 | t0023 | g0040 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00639 | hp2 | a0004 | c0004 | t0005 | g0256 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00642 | hp2 | a0003 | c0003 | t0002 | g0021 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00735 | hp1 | a0005 | c0012 | t0001 | g0035 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00735 | hp2 | a0002 | c0002 | t0011 | g0283 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00738 | hp2 | a0002 | c0002 | t0003 | g0096 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG00741 | hp2 | a0003 | c0005 | t0002 | g0052 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01070 | hp1 | a0003 | c0003 | t0002 | g0170 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01070 | hp2 | a0007 | c0020 | t0009 | g0003 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01071 | hp2 | a0007 | c0020 | t0009 | g0003 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01074 | hp2 | a0003 | c0003 | t0002 | g0175 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01099 | hp1 | a0001 | c0030 | t0001 | g0091 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01099 | hp2 | a0003 | c0003 | t0002 | g0173 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01106 | hp1 | a0004 | c0004 | t0005 | g0263 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01106 | hp2 | a0001 | c0001 | t0027 | g0224 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01109 | hp1 | a0003 | c0023 | t0002 | g0009 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01167 | hp2 | a0003 | c0005 | t0002 | g0070 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01168 | hp1 | a0002 | c0002 | t0003 | g0101 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01168 | hp2 | a0003 | c0005 | t0002 | g0069 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01175 | hp1 | a0004 | c0004 | t0005 | g0246 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01175 | hp2 | a0003 | c0005 | t0012 | g0079 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01243 | hp1 | a0004 | c0019 | t0020 | g0303 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01243 | hp2 | a0003 | c0008 | t0009 | g0088 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01255 | hp2 | a0002 | c0002 | t0010 | g0118 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01257 | hp1 | a0002 | c0002 | t0003 | g0134 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01257 | hp2 | a0003 | c0003 | t0007 | g0311 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01258 | hp1 | a0002 | c0002 | t0003 | g0116 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01258 | hp2 | a0003 | c0003 | t0002 | g0253 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01261 | hp1 | a0002 | c0002 | t0003 | g0115 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01261 | hp2 | a0001 | c0010 | t0001 | g0080 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01358 | hp1 | a0002 | c0006 | t0004 | g0024 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01361 | hp1 | a0004 | c0004 | t0005 | g0259 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01433 | hp1 | a0004 | c0004 | t0005 | g0268 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01433 | hp2 | a0003 | c0008 | t0009 | g0294 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01496 | hp2 | a0002 | c0006 | t0004 | g0025 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0225 | EUR | IBS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01515 | hp2 | a0004 | c0004 | t0025 | g0266 | EUR | IBS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01516 | hp1 | a0004 | c0004 | t0005 | g0089 | EUR | IBS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01516 | hp2 | a0004 | c0004 | t0005 | g0267 | EUR | IBS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01884 | hp1 | a0003 | c0036 | t0009 | g0308 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01928 | hp1 | a0002 | c0002 | t0003 | g0111 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01934 | hp1 | a0002 | c0002 | t0003 | g0113 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01943 | hp2 | a0002 | c0006 | t0004 | g0018 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG01981 | hp2 | a0002 | c0002 | t0003 | g0094 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02004 | hp2 | a0002 | c0002 | t0003 | g0107 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02015 | hp2 | a0002 | c0002 | t0003 | g0149 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02027 | hp1 | a0003 | c0005 | t0002 | g0059 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02027 | hp2 | a0001 | c0001 | t0013 | g0187 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02055 | hp1 | a0003 | c0005 | t0004 | g0076 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02055 | hp2 | a0003 | c0003 | t0025 | g0285 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02056 | hp1 | a0002 | c0002 | t0003 | g0147 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02071 | hp2 | a0003 | c0005 | t0002 | g0055 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02074 | hp2 | a0002 | c0002 | t0003 | g0155 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02083 | hp1 | a0001 | c0001 | t0029 | g0189 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02083 | hp2 | a0002 | c0002 | t0003 | g0154 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02135 | hp1 | a0003 | c0003 | t0007 | g0110 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02135 | hp2 | a0001 | c0010 | t0001 | g0064 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02145 | hp1 | a0003 | c0008 | t0008 | g0289 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02145 | hp2 | a0002 | c0006 | t0004 | g0023 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02148 | hp1 | a0003 | c0003 | t0002 | g0019 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02148 | hp2 | a0002 | c0002 | t0003 | g0148 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02155 | hp1 | a0003 | c0003 | t0007 | g0135 | EAS | CDX | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02155 | hp2 | a0002 | c0002 | t0012 | g0194 | EAS | CDX | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02257 | hp1 | a0003 | c0005 | t0002 | g0074 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02257 | hp2 | a0003 | c0007 | t0008 | g0072 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02258 | hp1 | a0003 | c0009 | t0032 | g0287 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02258 | hp2 | a0004 | c0004 | t0019 | g0290 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02280 | hp2 | a0003 | c0007 | t0036 | g0053 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02300 | hp1 | a0002 | c0002 | t0003 | g0120 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02451 | hp1 | a0001 | c0011 | t0001 | g0001 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02451 | hp2 | a0002 | c0014 | t0038 | g0043 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02572 | hp1 | a0008 | c0018 | t0010 | g0067 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02572 | hp2 | a0001 | c0022 | t0004 | g0010 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02602 | hp1 | a0002 | c0002 | t0006 | g0159 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02602 | hp2 | a0001 | c0010 | t0001 | g0054 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02615 | hp1 | a0004 | c0015 | t0005 | g0083 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02615 | hp2 | a0003 | c0003 | t0004 | g0257 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02622 | hp1 | a0003 | c0009 | t0016 | g0305 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02622 | hp2 | a0004 | c0004 | t0005 | g0309 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02630 | hp1 | a0003 | c0008 | t0046 | g0286 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02630 | hp2 | a0003 | c0003 | t0002 | g0172 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02647 | hp1 | a0008 | c0018 | t0010 | g0068 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02647 | hp2 | a0004 | c0004 | t0014 | g0297 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02683 | hp1 | a0001 | c0001 | t0034 | g0214 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02683 | hp2 | a0004 | c0004 | t0005 | g0255 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02723 | hp1 | a0003 | c0005 | t0002 | g0050 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02723 | hp2 | a0003 | c0009 | t0031 | g0033 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02735 | hp1 | a0002 | c0002 | t0003 | g0157 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02735 | hp2 | a0004 | c0004 | t0005 | g0227 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02738 | hp1 | a0004 | c0004 | t0021 | g0251 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02738 | hp2 | a0004 | c0004 | t0045 | g0312 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02809 | hp1 | a0002 | c0002 | t0011 | g0281 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02809 | hp2 | a0002 | c0002 | t0023 | g0087 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02886 | hp1 | a0002 | c0014 | t0018 | g0041 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02886 | hp2 | a0005 | c0012 | t0002 | g0034 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02895 | hp1 | a0003 | c0007 | t0008 | g0046 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02895 | hp2 | a0001 | c0011 | t0001 | g0082 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02897 | hp1 | a0003 | c0009 | t0026 | g0031 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02897 | hp2 | a0003 | c0007 | t0008 | g0047 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02922 | hp1 | a0004 | c0004 | t0001 | g0300 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02922 | hp2 | a0002 | c0014 | t0018 | g0042 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02965 | hp1 | a0002 | c0034 | t0035 | g0029 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02965 | hp2 | a0002 | c0028 | t0041 | g0280 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02970 | hp1 | a0001 | c0011 | t0001 | g0081 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02970 | hp2 | a0003 | c0008 | t0008 | g0291 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02976 | hp1 | a0004 | c0004 | t0005 | g0288 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02976 | hp2 | a0002 | c0017 | t0011 | g0075 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03017 | hp1 | a0002 | c0002 | t0003 | g0095 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03017 | hp2 | a0001 | c0001 | t0010 | g0099 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03041 | hp1 | a0004 | c0015 | t0018 | g0044 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03041 | hp2 | a0004 | c0004 | t0005 | g0249 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03098 | hp1 | a0003 | c0005 | t0002 | g0073 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03098 | hp2 | a0009 | c0026 | t0011 | g0284 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03139 | hp1 | a0005 | c0016 | t0014 | g0038 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03195 | hp1 | a0001 | c0011 | t0001 | g0086 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03195 | hp2 | a0005 | c0012 | t0002 | g0032 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03209 | hp1 | a0003 | c0005 | t0002 | g0051 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03209 | hp2 | a0004 | c0004 | t0030 | g0293 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03225 | hp1 | a0003 | c0009 | t0008 | g0307 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03225 | hp2 | a0003 | c0008 | t0009 | g0292 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03453 | hp1 | a0003 | c0005 | t0001 | g0085 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03453 | hp2 | a0009 | c0033 | t0001 | g0302 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03486 | hp1 | a0003 | c0009 | t0009 | g0306 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03486 | hp2 | a0003 | c0003 | t0004 | g0298 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03490 | hp1 | a0004 | c0004 | t0005 | g0197 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03490 | hp2 | a0003 | c0003 | t0002 | g0011 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03492 | hp1 | a0003 | c0003 | t0002 | g0017 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03540 | hp1 | a0004 | c0035 | t0009 | g0295 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03540 | hp2 | a0003 | c0032 | t0016 | g0313 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03654 | hp1 | a0002 | c0002 | t0003 | g0104 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03688 | hp1 | a0004 | c0004 | t0005 | g0228 | SAS | STU | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03688 | hp2 | a0003 | c0003 | t0001 | g0234 | SAS | STU | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03704 | hp1 | a0002 | c0002 | t0003 | g0158 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03704 | hp2 | a0003 | c0003 | t0002 | g0020 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03710 | hp2 | a0003 | c0005 | t0002 | g0056 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03831 | hp1 | a0003 | c0003 | t0002 | g0188 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03834 | hp1 | a0004 | c0004 | t0005 | g0250 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03834 | hp2 | a0003 | c0005 | t0002 | g0276 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03927 | hp1 | a0004 | c0004 | t0021 | g0258 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03927 | hp2 | a0003 | c0003 | t0007 | g0310 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03942 | hp1 | a0005 | c0016 | t0005 | g0233 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03942 | hp2 | a0003 | c0005 | t0002 | g0078 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18612 | hp1 | a0002 | c0027 | t0039 | g0114 | EAS | CHB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18612 | hp2 | a0002 | c0002 | t0003 | g0151 | EAS | CHB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18906 | hp1 | a0003 | c0007 | t0016 | g0060 | AFR | YRI | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18906 | hp2 | a0003 | c0005 | t0002 | g0066 | AFR | YRI | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18942 | hp1 | a0001 | c0001 | t0013 | g0167 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18942 | hp2 | a0002 | c0002 | t0003 | g0103 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18943 | hp1 | a0003 | c0003 | t0044 | g0109 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18943 | hp2 | a0003 | c0005 | t0002 | g0062 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18945 | hp2 | a0006 | c0013 | t0007 | g0137 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18946 | hp1 | a0001 | c0001 | t0017 | g0131 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18946 | hp2 | a0003 | c0003 | t0007 | g0119 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18950 | hp1 | a0002 | c0002 | t0003 | g0121 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18951 | hp1 | a0002 | c0002 | t0003 | g0146 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18951 | hp2 | a0002 | c0017 | t0006 | g0007 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18952 | hp1 | a0002 | c0002 | t0003 | g0125 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18952 | hp2 | a0003 | c0003 | t0002 | g0177 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18954 | hp1 | a0003 | c0003 | t0007 | g0105 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18956 | hp1 | a0006 | c0013 | t0002 | g0012 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18956 | hp2 | a0002 | c0002 | t0012 | g0179 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18959 | hp2 | a0002 | c0002 | t0003 | g0126 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18969 | hp1 | a0002 | c0006 | t0004 | g0169 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18969 | hp2 | a0003 | c0005 | t0002 | g0058 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18970 | hp2 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18971 | hp1 | a0001 | c0001 | t0010 | g0163 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18971 | hp2 | a0002 | c0002 | t0007 | g0141 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18973 | hp2 | a0002 | c0002 | t0003 | g0117 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18979 | hp1 | a0002 | c0002 | t0003 | g0106 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18979 | hp2 | a0001 | c0001 | t0012 | g0165 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18980 | hp2 | a0002 | c0002 | t0003 | g0124 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18982 | hp1 | a0003 | c0003 | t0017 | g0132 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18982 | hp2 | a0003 | c0003 | t0002 | g0178 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18983 | hp1 | a0001 | c0001 | t0043 | g0139 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18984 | hp1 | a0002 | c0002 | t0003 | g0098 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18984 | hp2 | a0010 | c0029 | t0001 | g0241 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18986 | hp2 | a0003 | c0005 | t0015 | g0008 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18988 | hp1 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18988 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18990 | hp1 | a0003 | c0005 | t0033 | g0077 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18990 | hp2 | a0002 | c0002 | t0003 | g0102 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18991 | hp1 | a0002 | c0002 | t0003 | g0108 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18991 | hp2 | a0002 | c0006 | t0004 | g0217 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18992 | hp1 | a0003 | c0005 | t0015 | g0071 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18992 | hp2 | a0001 | c0001 | t0013 | g0205 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18994 | hp1 | a0002 | c0002 | t0040 | g0143 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18994 | hp2 | a0001 | c0001 | t0006 | g0182 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18998 | hp1 | a0001 | c0001 | t0010 | g0112 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18998 | hp2 | a0002 | c0002 | t0003 | g0123 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18999 | hp1 | a0003 | c0003 | t0007 | g0136 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA18999 | hp2 | a0002 | c0006 | t0004 | g0211 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19000 | hp1 | a0002 | c0002 | t0003 | g0153 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19000 | hp2 | a0001 | c0001 | t0010 | g0162 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19001 | hp1 | a0001 | c0001 | t0017 | g0130 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19001 | hp2 | a0001 | c0010 | t0015 | g0006 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19002 | hp2 | a0002 | c0002 | t0003 | g0122 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19004 | hp1 | a0002 | c0002 | t0042 | g0127 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19005 | hp1 | a0002 | c0002 | t0024 | g0152 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19007 | hp1 | a0002 | c0002 | t0012 | g0242 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19007 | hp2 | a0001 | c0001 | t0022 | g0171 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19011 | hp1 | a0002 | c0006 | t0004 | g0022 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19012 | hp1 | a0003 | c0005 | t0002 | g0061 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19012 | hp2 | a0002 | c0006 | t0004 | g0210 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19030 | hp1 | a0004 | c0019 | t0020 | g0304 | AFR | LWK | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19043 | hp1 | a0003 | c0003 | t0004 | g0299 | AFR | LWK | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19043 | hp2 | a0004 | c0004 | t0019 | g0028 | AFR | LWK | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19057 | hp1 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19057 | hp2 | a0006 | c0021 | t0002 | g0016 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19058 | hp1 | a0011 | c0025 | t0003 | g0097 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19058 | hp2 | a0002 | c0006 | t0004 | g0164 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19063 | hp1 | a0003 | c0005 | t0002 | g0045 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19064 | hp1 | a0002 | c0006 | t0004 | g0014 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19064 | hp2 | a0001 | c0010 | t0001 | g0065 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19065 | hp1 | a0002 | c0002 | t0003 | g0129 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19066 | hp1 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19066 | hp2 | a0002 | c0002 | t0003 | g0145 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19070 | hp1 | a0002 | c0002 | t0003 | g0150 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19074 | hp1 | a0002 | c0002 | t0003 | g0140 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19076 | hp1 | a0002 | c0002 | t0024 | g0156 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19076 | hp2 | a0006 | c0013 | t0002 | g0093 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19078 | hp1 | a0001 | c0031 | t0006 | g0185 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19078 | hp2 | a0002 | c0002 | t0003 | g0133 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19079 | hp1 | a0001 | c0001 | t0047 | g0100 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19079 | hp2 | a0002 | c0006 | t0004 | g0015 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19081 | hp1 | a0001 | c0001 | t0013 | g0204 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19081 | hp2 | a0002 | c0002 | t0003 | g0144 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19084 | hp2 | a0003 | c0003 | t0002 | g0183 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19085 | hp1 | a0003 | c0005 | t0002 | g0057 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19087 | hp1 | a0002 | c0002 | t0003 | g0138 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19088 | hp2 | a0006 | c0013 | t0002 | g0026 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19091 | hp2 | a0002 | c0002 | t0003 | g0128 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19240 | hp1 | a0004 | c0004 | t0028 | g0027 | AFR | YRI | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA19240 | hp2 | a0005 | c0012 | t0002 | g0030 | AFR | YRI | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA20129 | hp1 | a0001 | c0011 | t0001 | g0001 | AFR | ASW | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA20129 | hp2 | a0004 | c0004 | t0004 | g0296 | AFR | ASW | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA20752 | hp1 | a0003 | c0005 | t0002 | g0039 | EUR | TSI | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02559 | hp1 | a0003 | c0007 | t0008 | g0049 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG02559 | hp2 | a0002 | c0002 | t0011 | g0036 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03471 | hp1 | a0002 | c0002 | t0011 | g0282 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG03471 | hp2 | a0003 | c0007 | t0008 | g0048 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG06807 | hp1 | a0005 | c0016 | t0014 | g0037 | AFR | USA | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
HG06807 | hp2 | a0003 | c0003 | t0002 | g0229 | AFR | USA | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA20300 | hp1 | a0002 | c0002 | t0010 | g0279 | AFR | USA | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
NA20300 | hp2 | a0004 | c0004 | t0001 | g0301 | AFR | USA | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0005 | REF | REF | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
homoSapiens | grch38p0 | a0004 | c0015 | t0004 | g0084 | REF | REF | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:20975096 | G | C | 1 | a0007 | 2 | HG01070.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.3041C>G | p.Ala1014Gly | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 3486/5546 | 3041/3267 | 1014/1088 | chr13 | 20975096 | |||
chr13:20975100 | C | T | 1 | a0001 | 5 | HG02451.hp1 HG02895.hp2 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.3037G>A | p.Asp1013Asn | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 3482/5546 | 3037/3267 | 1013/1088 | chr13 | 20975100 | |||
chr13:20981575 | G | C | 1 | a0001 | 5 | HG02451.hp1 HG02895.hp2 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.2556C>G | p.Asp852Glu | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/8 | 3001/5546 | 2556/3267 | 852/1088 | chr13 | 20981575 | |||
chr13:20983392 | T | C | 1 | a0008 | 2 | HG02572.hp1 HG02647.hp1 |
missense_variant | MODERATE | c.2314A>G | p.Ile772Val | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/8 | 2759/5546 | 2314/3267 | 772/1088 | chr13 | 20983392 | |||
chr13:20988093 | C | T | 1 | a0001 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1687G>A | p.Gly563Arg | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 2132/5546 | 1687/3267 | 563/1088 | chr13 | 20988093 | |||
chr13:20988343 | C | CGGGGCG | 3 | a0001 a0005 a0009 |
109 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(106): Show |
disruptive_inframe_insertion | MODERATE | c.1431_1436dupCGCCCC | p.Pro479_Ala480insAl others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1881/5546 | 1436/3267 | 479/1088 | chr13 | 20988343 | |||
chr13:20988343 | C | CGGGGCGG others(5): Show |
1 | a0010 | 1 | NA18984.hp2 | disruptive_inframe_insertion | MODERATE | c.1425_1436dupCGCCCC others(6): Show |
p.Pro479_Ala480insAl others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1881/5546 | 1436/3267 | 479/1088 | chr13 | 20988343 | |||
chr13:20988693 | C | T | 9 | a0001 a0002 a0003 others(6): Show |
274 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
missense_variant | MODERATE | c.1087G>A | p.Gly363Ser | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1532/5546 | 1087/3267 | 363/1088 | chr13 | 20988693 | |||
chr13:20988809 | G | A | 6 | a0001 a0003 a0006 others(3): Show |
188 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(185): Show |
missense_variant | MODERATE | c.971C>T | p.Ala324Val | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1416/5546 | 971/3267 | 324/1088 | chr13 | 20988809 | |||
chr13:20989172 | G | A | 1 | a0006 | 5 | NA18945.hp2 NA18956.hp1 NA19057.hp2 others(2): Show |
missense_variant | MODERATE | c.608C>T | p.Ala203Val | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1053/5546 | 608/3267 | 203/1088 | chr13 | 20989172 | |||
chr13:20989181 | C | G | 1 | a0011 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.599G>C | p.Gly200Ala | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1044/5546 | 599/3267 | 200/1088 | chr13 | 20989181 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:20975125 | G | A | 1 | a0002c0027 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.3012C>T | p.Pro1004Pro | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 3457/5546 | 3012/3267 | 1004/1088 | chr13 | 20975125 | |||
chr13:20975215 | G | A | 1 | a0002c0034 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.2922C>T | p.Ser974Ser | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 3367/5546 | 2922/3267 | 974/1088 | chr13 | 20975215 | |||
chr13:20975245 | G | A | 6 | a0002c0028 a0003c0007 a0003c0008 others(3): Show |
22 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(19): Show |
synonymous_variant | LOW | c.2892C>T | p.Ala964Ala | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 3337/5546 | 2892/3267 | 964/1088 | chr13 | 20975245 | |||
chr13:20981470 | G | A | 1 | a0004c0019 | 2 | HG01243.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.2661C>T | p.Arg887Arg | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/8 | 3106/5546 | 2661/3267 | 887/1088 | chr13 | 20981470 | |||
chr13:20981557 | C | T | 1 | a0001c0031 | 1 | NA19078.hp1 | synonymous_variant | LOW | c.2574G>A | p.Glu858Glu | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/8 | 3019/5546 | 2574/3267 | 858/1088 | chr13 | 20981557 | |||
chr13:20983240 | G | C | 1 | a0003c0032 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.2466C>G | p.Ser822Ser | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/8 | 2911/5546 | 2466/3267 | 822/1088 | chr13 | 20983240 | |||
chr13:20983591 | C | T | 1 | a0001c0030 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.2115G>A | p.Leu705Leu | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/8 | 2560/5546 | 2115/3267 | 705/1088 | chr13 | 20983591 | |||
chr13:20983780 | C | T | 1 | a0003c0023 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1926G>A | p.Glu642Glu | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/8 | 2371/5546 | 1926/3267 | 642/1088 | chr13 | 20983780 | |||
chr13:20988178 | G | A | 2 | a0003c0009 a0003c0036 |
7 | HG01884.hp1 HG02258.hp1 HG02622.hp1 others(4): Show |
synonymous_variant | LOW | c.1602C>T | p.Asp534Asp | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 2047/5546 | 1602/3267 | 534/1088 | chr13 | 20988178 | |||
chr13:20988223 | C | T | 1 | a0001c0022 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1557G>A | p.Pro519Pro | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 2002/5546 | 1557/3267 | 519/1088 | chr13 | 20988223 | |||
chr13:20988232 | C | T | 2 | a0002c0006 a0002c0014 |
17 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(14): Show |
synonymous_variant | LOW | c.1548G>A | p.Pro516Pro | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1993/5546 | 1548/3267 | 516/1088 | chr13 | 20988232 | |||
chr13:20988373 | A | T | 1 | a0001c0022 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1407T>A | p.Pro469Pro | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1852/5546 | 1407/3267 | 469/1088 | chr13 | 20988373 | |||
chr13:20988487 | G | A | 1 | a0005c0012 | 4 | HG00735.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.1293C>T | p.Thr431Thr | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1738/5546 | 1293/3267 | 431/1088 | chr13 | 20988487 | |||
chr13:20988940 | C | A | 3 | a0002c0024 a0002c0034 a0009c0033 |
3 | HG00639.hp1 HG02965.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.840G>T | p.Pro280Pro | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1285/5546 | 840/3267 | 280/1088 | chr13 | 20988940 | |||
chr13:20989021 | G | A | 1 | a0004c0035 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.759C>T | p.Tyr253Tyr | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1204/5546 | 759/3267 | 253/1088 | chr13 | 20989021 | |||
chr13:21045889 | G | A | 1 | a0003c0036 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.138C>T | p.Ser46Ser | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/8 | 583/5546 | 138/3267 | 46/1088 | chr13 | 21045889 | |||
chr13:21045946 | T | C | 25 | a0001c0001 a0001c0030 a0001c0031 others(22): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
synonymous_variant | LOW | c.81A>G | p.Lys27Lys | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/8 | 526/5546 | 81/3267 | 27/1088 | chr13 | 21045946 | |||
chr13:21046000 | C | T | 1 | a0006c0021 | 1 | NA19057.hp2 | synonymous_variant | LOW | c.27G>A | p.Thr9Thr | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/8 | 472/5546 | 27/3267 | 9/1088 | chr13 | 21046000 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:20973092 | G | T | 1 | a0001c0001t0034 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1778C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1778 | chr13 | 20973092 | ||||||
chr13:20973178 | T | C | 16 | a0001c0001t0002 a0001c0001t0027 a0001c0010t0015 others(13): Show |
69 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1692A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1692 | chr13 | 20973178 | ||||||
chr13:20973242 | T | C | 1 | a0001c0001t0029 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1628A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1628 | chr13 | 20973242 | ||||||
chr13:20973514 | C | CTG | 7 | a0002c0002t0023 a0002c0024t0023 a0004c0004t0014 others(4): Show |
9 | HG00639.hp1 HG02258.hp2 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1354_*1355dupCA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1355 | chr13 | 20973514 | ||||||
chr13:20973514 | C | CTGTG | 13 | a0001c0001t0003 a0001c0001t0012 a0002c0002t0003 others(10): Show |
62 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1352_*1355dupCACA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1355 | chr13 | 20973514 | ||||||
chr13:20973514 | C | CTGTGTG | 7 | a0001c0001t0006 a0001c0001t0029 a0001c0031t0006 others(4): Show |
12 | HG00423.hp1 HG02071.hp1 HG02083.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1350_*1355dupCACA others(2): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1355 | chr13 | 20973514 | ||||||
chr13:20973514 | CTG | C | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0010 others(43): Show |
174 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1354_*1355delCA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1354 | chr13 | 20973514 | ||||||
chr13:20973557 | C | T | 1 | a0002c0027t0039 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1313G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1313 | chr13 | 20973557 | ||||||
chr13:20973595 | T | G | 1 | a0003c0009t0032 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1275A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1275 | chr13 | 20973595 | ||||||
chr13:20973622 | T | A | 1 | a0001c0001t0022 | 2 | HG00438.hp1 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1248A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1248 | chr13 | 20973622 | ||||||
chr13:20973693 | A | G | 17 | a0002c0028t0041 a0003c0007t0008 a0003c0007t0016 others(14): Show |
25 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1177T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1177 | chr13 | 20973693 | ||||||
chr13:20973720 | A | T | 1 | a0004c0004t0019 | 2 | HG02258.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1150T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1150 | chr13 | 20973720 | ||||||
chr13:20973845 | C | T | 28 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0012 others(25): Show |
85 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1025G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1025 | chr13 | 20973845 | ||||||
chr13:20973887 | A | G | 88 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(85): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*983T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 983 | chr13 | 20973887 | ||||||
chr13:20973912 | C | T | 1 | a0004c0004t0028 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*958G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 958 | chr13 | 20973912 | ||||||
chr13:20973971 | T | TC | 43 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0012 others(40): Show |
123 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*898dupG | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 898 | chr13 | 20973971 | ||||||
chr13:20973971 | TC | T | 14 | a0001c0001t0002 a0001c0001t0027 a0001c0010t0015 others(11): Show |
67 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*898delG | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 898 | chr13 | 20973971 | ||||||
chr13:20974024 | TCA | T | 4 | a0001c0001t0013 a0001c0001t0017 a0001c0001t0043 others(1): Show |
8 | HG02027.hp2 NA18942.hp1 NA18946.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*844_*845delTG | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 844 | chr13 | 20974024 | ||||||
chr13:20974056 | A | G | 1 | a0004c0004t0019 | 2 | HG02258.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*814T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 814 | chr13 | 20974056 | ||||||
chr13:20974418 | G | A | 1 | a0002c0002t0042 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 452 | chr13 | 20974418 | ||||||
chr13:20974423 | C | CT | 30 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0012 others(27): Show |
91 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*446dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 446 | chr13 | 20974423 | ||||||
chr13:20974632 | C | T | 4 | a0002c0002t0011 a0002c0014t0038 a0002c0017t0011 others(1): Show |
7 | HG00735.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*238G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 238 | chr13 | 20974632 | ||||||
chr13:20974733 | A | G | 1 | a0001c0001t0027 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 137 | chr13 | 20974733 | ||||||
chr13:20974757 | G | A | 1 | a0001c0001t0037 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 113 | chr13 | 20974757 | ||||||
chr13:21046056 | A | G | 1 | a0003c0009t0026 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/8 | 30 | chr13 | 21046056 | ||||||
chr13:21046083 | T | TA | 28 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0017 others(25): Show |
85 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(82): Show |
5_prime_UTR_variant | MODIFIER | c.-58dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/8 | 58 | chr13 | 21046083 | ||||||
chr13:21046182 | T | C | 1 | a0001c0001t0047 | 1 | NA19079.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-156A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/8 | chr13 | 21046182 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:20975746 | C | T | 84 | a0001c0001t0003g0161 a0001c0001t0006g0168 a0001c0001t0006g0182 others(81): Show |
84 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.2773-382G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20975746 | |||||||
chr13:20975769 | C | T | 8 | a0002c0002t0003g0094 a0002c0002t0003g0096 a0002c0002t0003g0107 others(5): Show |
8 | HG00738.hp2 HG01175.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2773-405G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20975769 | |||||||
chr13:20975779 | G | A | 10 | a0002c0024t0023g0040 a0004c0004t0014g0297 a0004c0004t0019g0028 others(7): Show |
10 | HG00639.hp1 HG01243.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2773-415C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20975779 | |||||||
chr13:20975926 | A | C | 179 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(176): Show |
182 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.2773-562T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20975926 | |||||||
chr13:20975999 | C | T | 287 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(284): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.2773-635G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20975999 | |||||||
chr13:20976135 | CTTG | C | 85 | a0001c0001t0003g0161 a0001c0001t0006g0168 a0001c0001t0006g0182 others(82): Show |
85 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.2773-774_2773-772d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20976135 | |||||||
chr13:20976330 | C | T | 1 | a0003c0008t0046g0286 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2773-966G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20976330 | |||||||
chr13:20976366 | G | A | 1 | a0002c0034t0035g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2773-1002C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20976366 | |||||||
chr13:20976534 | C | T | 1 | a0003c0003t0004g0299 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2773-1170G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20976534 | |||||||
chr13:20976704 | A | T | 107 | a0001c0001t0003g0161 a0001c0001t0006g0168 a0001c0001t0006g0182 others(104): Show |
107 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.2773-1340T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20976704 | |||||||
chr13:20976830 | T | C | 287 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(284): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.2773-1466A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20976830 | |||||||
chr13:20977310 | C | T | 5 | a0003c0003t0002g0011 a0003c0003t0002g0017 a0003c0003t0002g0019 others(2): Show |
5 | HG00642.hp2 HG02148.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.2773-1946G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977310 | |||||||
chr13:20977385 | CA | C | 86 | a0001c0001t0002g0223 a0001c0001t0003g0161 a0001c0001t0006g0168 others(83): Show |
86 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.2773-2022delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977385 | |||||||
chr13:20977493 | G | C | 1 | a0004c0004t0005g0268 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2773-2129C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977493 | |||||||
chr13:20977622 | A | ATAAT | 85 | a0001c0001t0003g0161 a0001c0001t0006g0168 a0001c0001t0006g0182 others(82): Show |
85 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.2772+2068_2772+206 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977622 | |||||||
chr13:20977631 | AATTAAAA others(28): Show |
A | 1 | a0001c0001t0001g0248 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2772+2025_2772+205 others(39): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977631 | |||||||
chr13:20977644 | A | AAGATGGT others(27): Show |
66 | a0001c0001t0002g0002 a0001c0001t0002g0166 a0001c0001t0002g0199 others(63): Show |
67 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.2772+2013_2772+204 others(38): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977644 | |||||||
chr13:20977644 | A | AAGATGGT others(61): Show |
9 | a0002c0024t0023g0040 a0003c0005t0002g0052 a0004c0004t0014g0297 others(6): Show |
9 | HG00639.hp1 HG00741.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2772+1979_2772+204 others(72): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977644 | |||||||
chr13:20977644 | A | AAGATGGT others(95): Show |
1 | a0001c0001t0006g0184 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2772+1945_2772+204 others(106): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977644 | |||||||
chr13:20977644 | A | AAGATGGT others(129): Show |
72 | a0001c0001t0003g0161 a0001c0001t0006g0168 a0001c0001t0006g0182 others(69): Show |
72 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.2772+2046_2772+204 others(140): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977644 | |||||||
chr13:20977644 | A | AAGATGGT others(163): Show |
3 | a0002c0002t0012g0179 a0004c0019t0020g0303 a0004c0019t0020g0304 |
3 | HG01243.hp1 NA18956.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2772+2046_2772+204 others(174): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977644 | |||||||
chr13:20977792 | T | A | 1 | a0001c0001t0001g0272 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2772+1899A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977792 | |||||||
chr13:20977793 | C | A | 1 | a0001c0001t0001g0272 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2772+1898G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977793 | |||||||
chr13:20977816 | A | G | 15 | a0001c0001t0004g0274 a0002c0006t0004g0014 a0002c0006t0004g0015 others(12): Show |
15 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.2772+1875T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977816 | |||||||
chr13:20977838 | T | C | 22 | a0002c0028t0041g0280 a0003c0007t0008g0046 a0003c0007t0008g0047 others(19): Show |
22 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2772+1853A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977838 | |||||||
chr13:20977845 | G | A | 74 | a0001c0001t0003g0161 a0001c0001t0006g0168 a0001c0001t0006g0182 others(71): Show |
74 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2772+1846C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977845 | |||||||
chr13:20977848 | G | C | 5 | a0003c0003t0007g0105 a0003c0003t0007g0110 a0003c0003t0007g0135 others(2): Show |
5 | HG02071.hp2 HG02135.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.2772+1843C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977848 | |||||||
chr13:20978018 | C | T | 3 | a0004c0004t0019g0028 a0004c0004t0019g0290 a0004c0004t0030g0293 |
3 | HG02258.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2772+1673G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978018 | |||||||
chr13:20978065 | G | A | 3 | a0004c0004t0019g0028 a0004c0004t0019g0290 a0004c0004t0030g0293 |
3 | HG02258.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2772+1626C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978065 | |||||||
chr13:20978072 | T | C | 84 | a0001c0001t0003g0161 a0001c0001t0006g0168 a0001c0001t0006g0182 others(81): Show |
84 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.2772+1619A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978072 | |||||||
chr13:20978129 | C | T | 67 | a0001c0001t0002g0002 a0001c0001t0002g0166 a0001c0001t0002g0199 others(64): Show |
68 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.2772+1562G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978129 | |||||||
chr13:20978132 | G | A | 1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2772+1559C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978132 | |||||||
chr13:20978303 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2772+1388C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978303 | |||||||
chr13:20978323 | C | T | 104 | a0001c0001t0003g0161 a0001c0001t0004g0274 a0001c0001t0006g0168 others(101): Show |
104 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2772+1368G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978323 | |||||||
chr13:20978396 | T | C | 85 | a0001c0001t0003g0161 a0001c0001t0004g0274 a0001c0001t0006g0168 others(82): Show |
85 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.2772+1295A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978396 | |||||||
chr13:20978399 | T | C | 85 | a0001c0001t0003g0161 a0001c0001t0004g0274 a0001c0001t0006g0168 others(82): Show |
85 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.2772+1292A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978399 | |||||||
chr13:20978512 | A | T | 5 | a0004c0004t0014g0297 a0004c0004t0019g0028 a0004c0004t0019g0290 others(2): Show |
5 | HG02258.hp2 HG02647.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2772+1179T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978512 | |||||||
chr13:20978642 | C | T | 1 | a0005c0012t0002g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2772+1049G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978642 | |||||||
chr13:20978951 | C | T | 1 | a0003c0005t0002g0069 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2772+740G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978951 | |||||||
chr13:20978959 | G | A | 84 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(81): Show |
85 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.2772+732C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978959 | |||||||
chr13:20979095 | T | C | 70 | a0001c0001t0002g0002 a0001c0001t0002g0166 a0001c0001t0002g0199 others(67): Show |
71 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.2772+596A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20979095 | |||||||
chr13:20979832 | C | T | 74 | a0001c0001t0003g0161 a0001c0001t0004g0274 a0001c0001t0006g0168 others(71): Show |
74 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2666-35G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20979832 | |||||||
chr13:20979978 | G | A | 3 | a0003c0007t0016g0060 a0003c0009t0026g0031 a0003c0009t0031g0033 |
3 | HG02723.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2666-181C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20979978 | |||||||
chr13:20980016 | T | C | 2 | a0001c0022t0004g0010 a0003c0032t0016g0313 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2666-219A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980016 | |||||||
chr13:20980078 | A | T | 208 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(205): Show |
211 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.2666-281T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980078 | |||||||
chr13:20980254 | A | C | 233 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(230): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.2666-457T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980254 | |||||||
chr13:20980258 | G | A | 1 | a0002c0006t0004g0018 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2666-461C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980258 | |||||||
chr13:20980273 | G | A | 4 | a0003c0005t0002g0066 a0004c0004t0030g0293 a0004c0035t0009g0295 others(1): Show |
4 | HG03209.hp2 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2666-476C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980273 | |||||||
chr13:20980359 | G | A | 16 | a0001c0001t0001g0092 a0001c0001t0034g0214 a0002c0006t0004g0014 others(13): Show |
16 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.2666-562C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980359 | |||||||
chr13:20980498 | G | A | 1 | a0003c0009t0009g0306 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2666-701C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980498 | |||||||
chr13:20980629 | C | T | 1 | a0004c0004t0005g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2666-832G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980629 | |||||||
chr13:20980645 | G | A | 74 | a0001c0001t0002g0002 a0001c0001t0002g0166 a0001c0001t0002g0199 others(71): Show |
76 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.2665+821C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980645 | |||||||
chr13:20980703 | A | G | 1 | a0002c0002t0003g0113 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2665+763T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980703 | |||||||
chr13:20980921 | C | T | 202 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(199): Show |
205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2665+545G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980921 | |||||||
chr13:20981230 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2665+236G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20981230 | |||||||
chr13:20981405 | C | G | 118 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(115): Show |
120 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2665+61G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20981405 | |||||||
chr13:20981406 | T | A | 118 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(115): Show |
120 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2665+60A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20981406 | |||||||
chr13:20981415 | G | A | 95 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(92): Show |
97 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.2665+51C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20981415 | |||||||
chr13:20981419 | GA | G | 3 | a0002c0024t0023g0040 a0002c0034t0035g0029 a0009c0033t0001g0302 |
3 | HG00639.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2665+46delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20981419 | |||||||
chr13:20981461 | T | C | 3 | a0002c0002t0003g0148 a0002c0002t0003g0153 a0002c0002t0024g0152 |
3 | HG02148.hp2 NA19000.hp1 NA19005.hp1 |
splice_region_variant&intron_variant | LOW | c.2665+5A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20981461 | |||||||
chr13:20981702 | T | C | 1 | a0004c0004t0030g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2483-54A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20981702 | |||||||
chr13:20981953 | C | T | 1 | a0003c0003t0002g0170 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2483-305G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20981953 | |||||||
chr13:20982059 | G | A | 5 | a0002c0002t0010g0279 a0002c0024t0023g0040 a0002c0028t0041g0280 others(2): Show |
5 | HG00639.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2483-411C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982059 | |||||||
chr13:20982342 | G | T | 1 | a0001c0001t0001g0271 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2483-694C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982342 | |||||||
chr13:20982365 | G | A | 1 | a0003c0009t0008g0307 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2483-717C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982365 | |||||||
chr13:20982374 | C | T | 21 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0007t0008g0046 others(18): Show |
21 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2483-726G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982374 | |||||||
chr13:20982407 | G | A | 7 | a0003c0009t0008g0307 a0003c0009t0009g0306 a0003c0009t0016g0305 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2483-759C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982407 | |||||||
chr13:20982468 | G | A | 63 | a0002c0002t0003g0094 a0002c0002t0003g0095 a0002c0002t0003g0096 others(60): Show |
63 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.2482+756C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982468 | |||||||
chr13:20982489 | T | C | 5 | a0002c0002t0010g0279 a0002c0024t0023g0040 a0002c0028t0041g0280 others(2): Show |
5 | HG00639.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2482+735A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982489 | |||||||
chr13:20982630 | G | A | 4 | a0001c0001t0001g0195 a0001c0001t0001g0219 a0001c0001t0001g0277 others(1): Show |
4 | HG02056.hp2 NA18954.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2482+594C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982630 | |||||||
chr13:20982861 | C | T | 14 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(11): Show |
14 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.2482+363G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982861 | |||||||
chr13:20982948 | C | T | 202 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(199): Show |
205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.2482+276G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982948 | |||||||
chr13:20982992 | C | CA | 108 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(105): Show |
109 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.2482+231dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982992 | |||||||
chr13:20982992 | C | CAA | 19 | a0001c0001t0002g0225 a0001c0011t0001g0001 a0001c0011t0001g0081 others(16): Show |
20 | HG00280.hp2 HG00597.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.2482+230_2482+231d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982992 | |||||||
chr13:20982992 | C | CAAA | 62 | a0001c0001t0002g0216 a0001c0001t0002g0223 a0001c0001t0002g0226 others(59): Show |
63 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.2482+229_2482+231d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982992 | |||||||
chr13:20982999 | A | AC | 3 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 |
3 | HG02451.hp2 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2482+224_2482+225i others(3): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982999 | |||||||
chr13:20983011 | A | AC | 11 | a0001c0001t0003g0161 a0001c0001t0004g0274 a0001c0001t0006g0168 others(8): Show |
11 | HG00423.hp1 HG02071.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.2482+212_2482+213i others(3): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20983011 | |||||||
chr13:20983187 | C | T | 1 | a0004c0015t0018g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2482+37G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20983187 | |||||||
chr13:20983961 | C | T | 17 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(14): Show |
17 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.1900-155G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20983961 | |||||||
chr13:20984016 | C | T | 1 | a0003c0003t0002g0188 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1900-210G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984016 | |||||||
chr13:20984056 | G | A | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1900-250C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984056 | |||||||
chr13:20984059 | T | C | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1900-253A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984059 | |||||||
chr13:20984087 | T | A | 5 | a0002c0002t0011g0036 a0002c0002t0011g0281 a0002c0002t0011g0282 others(2): Show |
5 | HG00735.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1900-281A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984087 | |||||||
chr13:20984125 | C | T | 271 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(268): Show |
274 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.1900-319G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984125 | |||||||
chr13:20984154 | G | C | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1900-348C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984154 | |||||||
chr13:20984184 | T | C | 5 | a0002c0002t0010g0279 a0002c0024t0023g0040 a0002c0028t0041g0280 others(2): Show |
5 | HG00639.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1900-378A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984184 | |||||||
chr13:20984266 | G | A | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1900-460C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984266 | |||||||
chr13:20984315 | T | G | 272 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(269): Show |
275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.1900-509A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984315 | |||||||
chr13:20984407 | A | G | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0252 |
3 | HG00099.hp1 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1900-601T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984407 | |||||||
chr13:20984489 | A | G | 1 | a0002c0002t0006g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1900-683T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984489 | |||||||
chr13:20984671 | A | G | 203 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(200): Show |
206 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1900-865T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984671 | |||||||
chr13:20984881 | A | G | 21 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0007t0008g0046 others(18): Show |
21 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1900-1075T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984881 | |||||||
chr13:20984884 | T | G | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1900-1078A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984884 | |||||||
chr13:20984912 | G | C | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1900-1106C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984912 | |||||||
chr13:20985001 | G | A | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1900-1195C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985001 | |||||||
chr13:20985148 | A | G | 185 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(182): Show |
188 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1900-1342T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985148 | |||||||
chr13:20985266 | T | C | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1900-1460A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985266 | |||||||
chr13:20985381 | T | C | 5 | a0002c0002t0011g0036 a0002c0002t0011g0281 a0002c0002t0011g0282 others(2): Show |
5 | HG00735.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1900-1575A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985381 | |||||||
chr13:20985474 | C | T | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1900-1668G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985474 | |||||||
chr13:20985518 | T | C | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1900-1712A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985518 | |||||||
chr13:20985521 | T | C | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1900-1715A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985521 | |||||||
chr13:20985622 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1900-1816G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985622 | |||||||
chr13:20985719 | T | C | 272 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(269): Show |
275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.1900-1913A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985719 | |||||||
chr13:20985732 | C | T | 21 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0007t0008g0046 others(18): Show |
21 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1900-1926G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985732 | |||||||
chr13:20985748 | T | A | 110 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(107): Show |
113 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1900-1942A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985748 | |||||||
chr13:20985839 | A | C | 4 | a0002c0002t0003g0102 a0002c0002t0003g0113 a0002c0002t0003g0115 others(1): Show |
4 | HG01255.hp2 HG01261.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1900-2033T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985839 | |||||||
chr13:20985851 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1899+2030C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985851 | |||||||
chr13:20985875 | G | A | 1 | a0002c0006t0004g0210 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1899+2006C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985875 | |||||||
chr13:20985882 | C | CT | 272 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(269): Show |
275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.1899+1998_1899+199 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985882 | |||||||
chr13:20985912 | T | C | 272 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(269): Show |
275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.1899+1969A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985912 | |||||||
chr13:20985969 | G | A | 21 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0007t0008g0046 others(18): Show |
21 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1899+1912C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985969 | |||||||
chr13:20985996 | A | G | 24 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0007t0008g0046 others(21): Show |
25 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1899+1885T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985996 | |||||||
chr13:20986005 | T | C | 64 | a0002c0002t0003g0094 a0002c0002t0003g0095 a0002c0002t0003g0096 others(61): Show |
64 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1899+1876A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20986005 | |||||||
chr13:20986257 | A | T | 308 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(305): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1899+1624T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20986257 | |||||||
chr13:20986296 | T | G | 1 | a0005c0016t0014g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1899+1585A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20986296 | |||||||
chr13:20986410 | T | C | 64 | a0002c0002t0003g0094 a0002c0002t0003g0095 a0002c0002t0003g0096 others(61): Show |
64 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1899+1471A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20986410 | |||||||
chr13:20986849 | G | T | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1899+1032C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20986849 | |||||||
chr13:20986952 | G | A | 2 | a0004c0019t0020g0303 a0004c0019t0020g0304 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1899+929C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20986952 | |||||||
chr13:20987195 | A | C | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1899+686T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987195 | |||||||
chr13:20987212 | AAAAAATA others(5): Show |
A | 69 | a0001c0001t0002g0216 a0001c0001t0002g0223 a0001c0001t0002g0225 others(66): Show |
70 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.1899+657_1899+668d others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987212 | |||||||
chr13:20987224 | T | TA | 196 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(193): Show |
198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1899+656dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987224 | |||||||
chr13:20987267 | G | C | 14 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(11): Show |
14 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1899+614C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987267 | |||||||
chr13:20987314 | A | C | 4 | a0001c0001t0001g0181 a0001c0001t0001g0200 a0001c0001t0001g0209 others(1): Show |
4 | HG00642.hp1 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1899+567T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987314 | |||||||
chr13:20987338 | ATC | A | 5 | a0002c0002t0010g0279 a0002c0024t0023g0040 a0002c0028t0041g0280 others(2): Show |
5 | HG00639.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1899+541_1899+542d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987338 | |||||||
chr13:20987402 | C | G | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1899+479G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987402 | |||||||
chr13:20987443 | A | G | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1899+438T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987443 | |||||||
chr13:20987498 | C | T | 1 | a0002c0017t0006g0007 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1899+383G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987498 | |||||||
chr13:20987624 | T | C | 3 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 |
3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1899+257A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987624 | |||||||
chr13:20987707 | G | A | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1899+174C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987707 | |||||||
chr13:20987736 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1899+145A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987736 | |||||||
chr13:20987826 | T | C | 2 | a0003c0003t0004g0257 a0003c0003t0025g0285 |
2 | HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1899+55A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987826 | |||||||
chr13:20989408 | G | T | 2 | a0002c0024t0023g0040 a0002c0034t0035g0029 |
2 | HG00639.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.476-104C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20989408 | |||||||
chr13:20989503 | G | C | 22 | a0002c0002t0010g0279 a0002c0006t0004g0014 a0002c0006t0004g0015 others(19): Show |
22 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.476-199C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20989503 | |||||||
chr13:20989576 | C | T | 271 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(268): Show |
274 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.476-272G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20989576 | |||||||
chr13:20989862 | TA | T | 13 | a0003c0003t0002g0011 a0003c0003t0002g0013 a0003c0003t0002g0017 others(10): Show |
13 | HG00642.hp2 HG02148.hp1 HG03490.hp2 others(10): Show |
intron_variant | MODIFIER | c.476-559delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20989862 | |||||||
chr13:20990121 | A | G | 309 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.476-817T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990121 | |||||||
chr13:20990148 | T | C | 22 | a0002c0002t0010g0279 a0002c0006t0004g0014 a0002c0006t0004g0015 others(19): Show |
22 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.476-844A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990148 | |||||||
chr13:20990152 | T | C | 1 | a0003c0005t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.476-848A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990152 | |||||||
chr13:20990340 | A | AATGTGTG others(312): Show |
1 | a0002c0006t0004g0023 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.475+931_475+932ins others(319): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990340 | |||||||
chr13:20990340 | A | AATGTGTG others(315): Show |
3 | a0002c0006t0004g0024 a0002c0006t0004g0025 a0002c0006t0004g0254 |
3 | HG00280.hp2 HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.475+931_475+932ins others(322): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990340 | |||||||
chr13:20990340 | A | AATGTGTG others(328): Show |
2 | a0002c0014t0018g0042 a0002c0014t0038g0043 |
2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.475+931_475+932ins others(335): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990340 | |||||||
chr13:20990340 | A | AATGTGTG others(329): Show |
7 | a0002c0006t0004g0014 a0002c0006t0004g0018 a0002c0006t0004g0022 others(4): Show |
7 | HG01943.hp2 HG02886.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.475+931_475+932ins others(336): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990340 | |||||||
chr13:20990340 | A | AATGTGTG others(330): Show |
3 | a0002c0006t0004g0015 a0002c0006t0004g0164 a0002c0006t0004g0217 |
3 | NA18991.hp2 NA19058.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.475+931_475+932ins others(337): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990340 | |||||||
chr13:20990340 | A | AATGTGTG others(332): Show |
1 | a0002c0006t0004g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.475+931_475+932ins others(339): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990340 | |||||||
chr13:20990411 | T | G | 1 | a0001c0001t0017g0131 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.475+861A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990411 | |||||||
chr13:20990413 | T | A | 1 | a0001c0001t0017g0131 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.475+859A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990413 | |||||||
chr13:20990461 | A | AT | 77 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(74): Show |
80 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.475+810dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | |||||||
chr13:20990461 | A | ATT | 14 | a0001c0001t0001g0193 a0001c0001t0001g0213 a0001c0001t0001g0230 others(11): Show |
14 | HG01358.hp2 HG02027.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.475+809_475+810dup others(2): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | |||||||
chr13:20990461 | A | ATTTTTTT | 33 | a0001c0001t0002g0223 a0001c0001t0002g0226 a0001c0001t0027g0224 others(30): Show |
33 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.475+804_475+810dup others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | |||||||
chr13:20990461 | A | ATTTTTTT others(1): Show |
28 | a0001c0001t0002g0216 a0001c0001t0002g0225 a0003c0003t0002g0013 others(25): Show |
28 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.475+803_475+810dup others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | |||||||
chr13:20990461 | A | ATTTTTTT others(2): Show |
12 | a0003c0003t0002g0188 a0003c0003t0004g0298 a0003c0003t0044g0109 others(9): Show |
12 | HG01433.hp2 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.475+802_475+810dup others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | |||||||
chr13:20990461 | A | ATTTTTTT others(3): Show |
2 | a0003c0005t0002g0055 a0003c0008t0046g0286 |
2 | HG02071.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.475+801_475+810dup others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | |||||||
chr13:20990461 | A | ATTTTTTT others(5): Show |
1 | a0003c0036t0009g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.475+799_475+810dup others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | |||||||
chr13:20990461 | A | ATTTTTTT others(6): Show |
2 | a0008c0018t0010g0067 a0008c0018t0010g0068 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.475+798_475+810dup others(13): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | |||||||
chr13:20990461 | AT | A | 80 | a0002c0002t0003g0095 a0002c0002t0003g0096 a0002c0002t0003g0101 others(77): Show |
80 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.475+810delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | |||||||
chr13:20990461 | ATT | A | 10 | a0002c0002t0003g0094 a0002c0002t0003g0098 a0002c0002t0003g0133 others(7): Show |
10 | HG00639.hp1 HG01981.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+809_475+810del others(2): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | |||||||
chr13:20990461 | ATTTTTTT others(2): Show |
A | 10 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(7): Show |
10 | HG00597.hp2 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.475+802_475+810del others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | |||||||
chr13:20990461 | ATTTTTTT others(3): Show |
A | 4 | a0002c0006t0004g0217 a0002c0014t0018g0041 a0002c0014t0018g0042 others(1): Show |
4 | HG02451.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.475+801_475+810del others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | |||||||
chr13:20990462 | T | A | 1 | a0001c0001t0017g0131 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.475+810A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990462 | |||||||
chr13:20990478 | TTTTTTTT others(3): Show |
T | 3 | a0003c0003t0002g0172 a0003c0003t0002g0173 a0003c0003t0002g0175 |
3 | HG01074.hp2 HG01099.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.475+784_475+793del others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990478 | |||||||
chr13:20990488 | A | T | 183 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(180): Show |
186 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.475+784T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990488 | |||||||
chr13:20990502 | T | A | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.475+770A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990502 | |||||||
chr13:20990598 | A | C | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.475+674T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990598 | |||||||
chr13:20991158 | T | G | 1 | a0003c0005t0002g0055 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.475+114A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20991158 | |||||||
chr13:20991209 | G | A | 1 | a0001c0001t0004g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.475+63C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20991209 | |||||||
chr13:20991581 | G | T | 1 | a0002c0014t0018g0042 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.343-177C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991581 | |||||||
chr13:20991714 | T | C | 1 | a0004c0004t0001g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.343-310A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991714 | |||||||
chr13:20991861 | C | T | 1 | a0003c0003t0002g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.343-457G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991861 | |||||||
chr13:20991880 | C | T | 2 | a0002c0002t0011g0036 a0002c0002t0011g0283 |
2 | HG00735.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.343-476G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991880 | |||||||
chr13:20991903 | T | C | 1 | a0003c0003t0025g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.343-499A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991903 | |||||||
chr13:20991927 | G | A | 64 | a0002c0002t0003g0094 a0002c0002t0003g0095 a0002c0002t0003g0096 others(61): Show |
64 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.343-523C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991927 | |||||||
chr13:20991947 | G | A | 1 | a0003c0005t0002g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.343-543C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991947 | |||||||
chr13:20991992 | C | A | 185 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(182): Show |
188 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.343-588G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991992 | |||||||
chr13:20992104 | C | A | 20 | a0003c0003t0004g0257 a0003c0007t0008g0046 a0003c0007t0008g0047 others(17): Show |
20 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.343-700G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992104 | |||||||
chr13:20992230 | A | G | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-826T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992230 | |||||||
chr13:20992236 | G | A | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-832C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992236 | |||||||
chr13:20992250 | T | C | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-846A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992250 | |||||||
chr13:20992258 | G | A | 18 | a0004c0004t0005g0004 a0004c0004t0005g0089 a0004c0004t0005g0197 others(15): Show |
18 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.343-854C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992258 | |||||||
chr13:20992325 | G | A | 26 | a0003c0009t0008g0307 a0003c0009t0009g0306 a0003c0009t0016g0305 others(23): Show |
26 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.343-921C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992325 | |||||||
chr13:20992379 | T | C | 2 | a0003c0008t0009g0292 a0003c0008t0009g0294 |
2 | HG01433.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.343-975A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992379 | |||||||
chr13:20992436 | C | T | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-1032G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992436 | |||||||
chr13:20992437 | G | A | 7 | a0001c0001t0002g0216 a0001c0001t0002g0223 a0001c0001t0002g0225 others(4): Show |
7 | HG00741.hp1 HG01081.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-1033C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992437 | |||||||
chr13:20992465 | G | A | 1 | a0001c0010t0001g0080 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.343-1061C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992465 | |||||||
chr13:20992548 | G | A | 4 | a0005c0012t0001g0035 a0005c0012t0002g0030 a0005c0012t0002g0032 others(1): Show |
4 | HG00735.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-1144C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992548 | |||||||
chr13:20992763 | G | A | 17 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(14): Show |
17 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.343-1359C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992763 | |||||||
chr13:20992774 | C | T | 4 | a0005c0012t0001g0035 a0005c0012t0002g0030 a0005c0012t0002g0032 others(1): Show |
4 | HG00735.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-1370G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992774 | |||||||
chr13:20992784 | C | T | 16 | a0001c0001t0001g0090 a0001c0001t0001g0192 a0001c0001t0001g0206 others(13): Show |
16 | HG00280.hp1 HG00738.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.343-1380G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992784 | |||||||
chr13:20992906 | G | T | 1 | a0003c0003t0002g0188 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.343-1502C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992906 | |||||||
chr13:20992969 | G | A | 1 | a0004c0004t0021g0258 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.343-1565C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992969 | |||||||
chr13:20993015 | A | T | 1 | a0002c0017t0011g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.343-1611T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993015 | |||||||
chr13:20993035 | C | CA | 59 | a0001c0001t0002g0223 a0001c0001t0002g0226 a0001c0022t0004g0010 others(56): Show |
59 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.343-1632dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | |||||||
chr13:20993035 | C | CAA | 10 | a0002c0002t0003g0155 a0002c0002t0012g0242 a0002c0002t0024g0156 others(7): Show |
11 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.343-1633_343-1632d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | |||||||
chr13:20993035 | CA | C | 27 | a0002c0002t0003g0128 a0002c0006t0004g0014 a0002c0006t0004g0015 others(24): Show |
27 | HG00280.hp2 HG00597.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.343-1632delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | |||||||
chr13:20993035 | CAA | C | 16 | a0003c0007t0008g0046 a0003c0007t0008g0047 a0003c0007t0008g0048 others(13): Show |
16 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.343-1633_343-1632d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | |||||||
chr13:20993035 | CAAAAAA | C | 7 | a0001c0001t0001g0261 a0001c0001t0006g0182 a0001c0001t0006g0184 others(4): Show |
7 | HG00738.hp1 HG02071.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-1637_343-1632d others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | |||||||
chr13:20993035 | CAAAAAAA | C | 85 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(82): Show |
87 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.343-1638_343-1632d others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | |||||||
chr13:20993035 | CAAAAAAA others(6): Show |
C | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-1644_343-1632d others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | |||||||
chr13:20993063 | G | C | 1 | a0002c0002t0011g0281 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.343-1659C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993063 | |||||||
chr13:20993063 | G | T | 1 | a0002c0002t0003g0146 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.343-1659C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993063 | |||||||
chr13:20993090 | G | A | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.343-1686C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993090 | |||||||
chr13:20993145 | C | T | 1 | a0005c0012t0002g0034 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.343-1741G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993145 | |||||||
chr13:20993397 | G | A | 1 | a0002c0002t0003g0094 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.343-1993C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993397 | |||||||
chr13:20993400 | A | G | 176 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(173): Show |
179 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.343-1996T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993400 | |||||||
chr13:20993432 | A | G | 185 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(182): Show |
188 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.343-2028T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993432 | |||||||
chr13:20993469 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.343-2065G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993469 | |||||||
chr13:20993689 | A | G | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-2285T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993689 | |||||||
chr13:20993799 | G | A | 1 | a0003c0005t0002g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.343-2395C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993799 | |||||||
chr13:20993830 | A | G | 64 | a0002c0002t0003g0094 a0002c0002t0003g0095 a0002c0002t0003g0096 others(61): Show |
64 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.343-2426T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993830 | |||||||
chr13:20994006 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.343-2602A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994006 | |||||||
chr13:20994167 | A | G | 1 | a0003c0005t0033g0077 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.343-2763T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994167 | |||||||
chr13:20994235 | C | T | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-2831G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994235 | |||||||
chr13:20994294 | A | G | 3 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 |
3 | HG02451.hp2 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.343-2890T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994294 | |||||||
chr13:20994393 | C | T | 1 | a0002c0002t0003g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.343-2989G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994393 | |||||||
chr13:20994512 | C | T | 1 | a0001c0001t0037g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.343-3108G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994512 | |||||||
chr13:20994632 | T | C | 185 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(182): Show |
188 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.343-3228A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994632 | |||||||
chr13:20994675 | G | T | 4 | a0001c0001t0002g0223 a0001c0001t0002g0225 a0001c0001t0002g0226 others(1): Show |
4 | HG00741.hp1 HG01106.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-3271C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994675 | |||||||
chr13:20994854 | C | CA | 67 | a0001c0001t0002g0166 a0001c0001t0004g0274 a0002c0002t0003g0094 others(64): Show |
67 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.343-3451dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994854 | |||||||
chr13:20994854 | C | CAA | 184 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(181): Show |
187 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.343-3452_343-3451d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994854 | |||||||
chr13:20994854 | C | CAAA | 19 | a0001c0001t0006g0182 a0002c0002t0010g0279 a0002c0006t0004g0014 others(16): Show |
19 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.343-3453_343-3451d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994854 | |||||||
chr13:20994868 | T | A | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-3464A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994868 | |||||||
chr13:20994955 | A | T | 4 | a0004c0004t0005g0263 a0004c0004t0005g0267 a0004c0004t0005g0268 others(1): Show |
4 | HG01106.hp1 HG01433.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-3551T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994955 | |||||||
chr13:20995088 | T | C | 22 | a0003c0003t0025g0285 a0004c0004t0005g0004 a0004c0004t0005g0089 others(19): Show |
22 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.343-3684A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995088 | |||||||
chr13:20995193 | AT | A | 5 | a0002c0002t0010g0279 a0002c0024t0023g0040 a0002c0028t0041g0280 others(2): Show |
5 | HG00639.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-3790delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995193 | |||||||
chr13:20995205 | G | A | 3 | a0004c0015t0018g0044 a0004c0019t0020g0303 a0004c0019t0020g0304 |
3 | HG01243.hp1 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.343-3801C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995205 | |||||||
chr13:20995206 | A | G | 64 | a0002c0002t0003g0094 a0002c0002t0003g0095 a0002c0002t0003g0096 others(61): Show |
64 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.343-3802T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995206 | |||||||
chr13:20995450 | T | G | 271 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(268): Show |
274 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.343-4046A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995450 | |||||||
chr13:20995505 | G | C | 3 | a0001c0001t0001g0231 a0001c0001t0010g0162 a0001c0001t0010g0163 |
3 | HG00423.hp2 NA18971.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.343-4101C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995505 | |||||||
chr13:20995576 | T | C | 1 | a0005c0012t0002g0034 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.343-4172A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995576 | |||||||
chr13:20995665 | A | G | 1 | a0002c0034t0035g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.343-4261T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995665 | |||||||
chr13:20995764 | T | TA | 66 | a0001c0001t0002g0216 a0001c0001t0002g0223 a0001c0001t0002g0225 others(63): Show |
66 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.343-4361dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995764 | |||||||
chr13:20995766 | T | A | 66 | a0001c0001t0002g0216 a0001c0001t0002g0223 a0001c0001t0002g0225 others(63): Show |
66 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.343-4362A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995766 | |||||||
chr13:20995845 | G | A | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343-4441C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995845 | |||||||
chr13:20995876 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.343-4472A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995876 | |||||||
chr13:20995910 | G | A | 21 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0007t0008g0046 others(18): Show |
21 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.343-4506C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995910 | |||||||
chr13:20996042 | A | G | 293 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(290): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.343-4638T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996042 | |||||||
chr13:20996062 | A | G | 2 | a0003c0009t0026g0031 a0003c0009t0031g0033 |
2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.343-4658T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996062 | |||||||
chr13:20996063 | G | C | 271 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(268): Show |
274 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.343-4659C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996063 | |||||||
chr13:20996107 | T | G | 185 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(182): Show |
188 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.343-4703A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996107 | |||||||
chr13:20996171 | C | T | 99 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(96): Show |
101 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.343-4767G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996171 | |||||||
chr13:20996322 | A | G | 1 | a0002c0002t0003g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.343-4918T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996322 | |||||||
chr13:20996377 | A | AT | 34 | a0001c0001t0001g0244 a0001c0001t0001g0260 a0001c0001t0001g0261 others(31): Show |
34 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.343-4974dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996377 | |||||||
chr13:20996377 | AT | A | 78 | a0001c0001t0001g0207 a0001c0001t0001g0240 a0001c0001t0013g0167 others(75): Show |
78 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.343-4974delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996377 | |||||||
chr13:20996377 | ATT | A | 33 | a0002c0002t0003g0104 a0002c0002t0007g0141 a0002c0002t0011g0036 others(30): Show |
34 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.343-4975_343-4974d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996377 | |||||||
chr13:20996377 | ATTT | A | 61 | a0001c0010t0015g0006 a0003c0003t0002g0011 a0003c0003t0002g0013 others(58): Show |
61 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.343-4976_343-4974d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996377 | |||||||
chr13:20996439 | C | T | 2 | a0001c0001t0003g0161 a0001c0001t0012g0165 |
2 | HG02074.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.343-5035G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996439 | |||||||
chr13:20996492 | C | T | 1 | a0001c0030t0001g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.343-5088G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996492 | |||||||
chr13:20996497 | C | G | 1 | a0005c0016t0005g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.343-5093G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996497 | |||||||
chr13:20996529 | C | T | 186 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(183): Show |
189 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.343-5125G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996529 | |||||||
chr13:20996679 | G | A | 1 | a0004c0004t0005g0259 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.343-5275C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996679 | |||||||
chr13:20996723 | T | C | 1 | a0002c0002t0003g0142 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.343-5319A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996723 | |||||||
chr13:20996773 | T | C | 24 | a0004c0004t0005g0004 a0004c0004t0005g0089 a0004c0004t0005g0197 others(21): Show |
24 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.343-5369A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996773 | |||||||
chr13:20997002 | G | A | 64 | a0002c0002t0003g0094 a0002c0002t0003g0095 a0002c0002t0003g0096 others(61): Show |
64 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.343-5598C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997002 | |||||||
chr13:20997118 | G | A | 186 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(183): Show |
189 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.343-5714C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997118 | |||||||
chr13:20997234 | C | T | 308 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(305): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.343-5830G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997234 | |||||||
chr13:20997305 | T | C | 26 | a0002c0002t0010g0279 a0002c0006t0004g0014 a0002c0006t0004g0015 others(23): Show |
26 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.343-5901A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997305 | |||||||
chr13:20997639 | A | G | 94 | a0002c0002t0003g0094 a0002c0002t0003g0095 a0002c0002t0003g0096 others(91): Show |
94 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.343-6235T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997639 | |||||||
chr13:20997789 | A | G | 4 | a0004c0004t0019g0028 a0004c0004t0019g0290 a0004c0004t0030g0293 others(1): Show |
4 | HG02258.hp2 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-6385T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997789 | |||||||
chr13:20997890 | G | C | 101 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(98): Show |
103 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.343-6486C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997890 | |||||||
chr13:20997979 | T | C | 99 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0191 others(96): Show |
99 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.343-6575A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997979 | |||||||
chr13:20997980 | G | A | 1 | a0002c0002t0003g0148 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.343-6576C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997980 | |||||||
chr13:20998140 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.343-6736G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998140 | |||||||
chr13:20998170 | G | A | 1 | a0003c0003t0002g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.343-6766C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998170 | |||||||
chr13:20998211 | G | A | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-6807C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998211 | |||||||
chr13:20998365 | A | T | 2 | a0001c0022t0004g0010 a0009c0033t0001g0302 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.343-6961T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998365 | |||||||
chr13:20998377 | TA | T | 108 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0001g0195 others(105): Show |
109 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.343-6974delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998377 | |||||||
chr13:20998513 | C | T | 2 | a0001c0001t0001g0213 a0003c0005t0002g0276 |
2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.343-7109G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998513 | |||||||
chr13:20998518 | G | GA | 3 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 |
3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.343-7115dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998518 | |||||||
chr13:20998634 | C | T | 4 | a0002c0002t0003g0126 a0002c0002t0003g0128 a0002c0002t0003g0129 others(1): Show |
4 | NA18959.hp2 NA19004.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-7230G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998634 | |||||||
chr13:20998648 | C | G | 301 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(298): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.343-7244G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998648 | |||||||
chr13:20998655 | T | C | 1 | a0002c0002t0003g0146 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.343-7251A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998655 | |||||||
chr13:20998690 | G | A | 10 | a0002c0002t0012g0242 a0002c0006t0004g0014 a0002c0006t0004g0018 others(7): Show |
10 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.343-7286C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998690 | |||||||
chr13:20998705 | A | C | 12 | a0001c0001t0002g0002 a0002c0002t0012g0242 a0002c0006t0004g0014 others(9): Show |
13 | HG00597.hp2 HG01943.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-7301T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998705 | |||||||
chr13:20998745 | G | GCGAGGCG others(9): Show |
50 | a0001c0001t0001g0222 a0001c0001t0001g0238 a0001c0001t0001g0260 others(47): Show |
50 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.343-7357_343-7342d others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998745 | |||||||
chr13:20998745 | G | GCGAGGCG others(10): Show |
4 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-7358_343-7342d others(19): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998745 | |||||||
chr13:20998752 | G | C | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-7348C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998752 | |||||||
chr13:20998992 | C | G | 2 | a0004c0004t0001g0300 a0004c0004t0001g0301 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-7588G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998992 | |||||||
chr13:20999024 | G | A | 1 | a0003c0007t0008g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.343-7620C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999024 | |||||||
chr13:20999320 | C | T | 1 | a0003c0023t0002g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.343-7916G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999320 | |||||||
chr13:20999362 | G | A | 82 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(79): Show |
84 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.343-7958C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999362 | |||||||
chr13:20999501 | C | A | 2 | a0002c0034t0035g0029 a0004c0004t0028g0027 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.343-8097G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999501 | |||||||
chr13:20999544 | T | C | 10 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-8140A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999544 | |||||||
chr13:20999606 | C | A | 7 | a0004c0004t0005g0197 a0004c0004t0005g0227 a0004c0004t0005g0228 others(4): Show |
7 | HG02735.hp2 HG02738.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-8202G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999606 | |||||||
chr13:20999634 | T | A | 11 | a0002c0002t0012g0242 a0003c0003t0004g0257 a0003c0003t0025g0285 others(8): Show |
11 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.343-8230A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999634 | |||||||
chr13:20999710 | A | C | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-8306T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999710 | |||||||
chr13:20999757 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.343-8353G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999757 | |||||||
chr13:20999863 | C | CA | 77 | a0001c0001t0001g0200 a0001c0001t0001g0237 a0001c0010t0001g0054 others(74): Show |
77 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.343-8460dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999863 | |||||||
chr13:20999863 | C | CAA | 186 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(183): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.343-8461_343-8460d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999863 | |||||||
chr13:20999863 | C | CAAA | 27 | a0001c0001t0001g0180 a0001c0001t0001g0220 a0001c0001t0001g0222 others(24): Show |
27 | HG00597.hp1 HG00738.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.343-8462_343-8460d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999863 | |||||||
chr13:20999888 | C | T | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-8484G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999888 | |||||||
chr13:20999983 | T | C | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-8579A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999983 | |||||||
chr13:21000078 | A | G | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343-8674T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000078 | |||||||
chr13:21000123 | T | C | 2 | a0004c0019t0020g0303 a0004c0019t0020g0304 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.343-8719A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000123 | |||||||
chr13:21000253 | C | T | 76 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(73): Show |
77 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.343-8849G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000253 | |||||||
chr13:21000378 | C | CATA | 19 | a0001c0001t0022g0171 a0002c0002t0003g0148 a0002c0002t0003g0153 others(16): Show |
19 | HG00597.hp2 HG01243.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.343-8977_343-8975d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000378 | |||||||
chr13:21000381 | A | C | 75 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(72): Show |
76 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.343-8977T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000381 | |||||||
chr13:21000384 | A | C | 3 | a0001c0022t0004g0010 a0002c0002t0010g0279 a0002c0028t0041g0280 |
3 | HG02572.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-8980T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000384 | |||||||
chr13:21000489 | G | A | 77 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(74): Show |
78 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.343-9085C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000489 | |||||||
chr13:21000503 | G | A | 4 | a0002c0002t0010g0279 a0002c0028t0041g0280 a0005c0016t0014g0037 others(1): Show |
4 | HG02965.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-9099C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000503 | |||||||
chr13:21000765 | T | C | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-9361A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000765 | |||||||
chr13:21000770 | T | C | 54 | a0001c0001t0002g0216 a0001c0001t0002g0223 a0001c0001t0002g0225 others(51): Show |
54 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.343-9366A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000770 | |||||||
chr13:21000795 | A | G | 1 | a0006c0013t0002g0012 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.343-9391T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000795 | |||||||
chr13:21000862 | G | T | 120 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(117): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.343-9458C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000862 | |||||||
chr13:21000866 | C | T | 7 | a0003c0007t0008g0046 a0003c0007t0008g0047 a0003c0007t0008g0048 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.343-9462G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000866 | |||||||
chr13:21000980 | A | G | 1 | a0002c0002t0003g0101 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.343-9576T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000980 | |||||||
chr13:21000993 | C | G | 299 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(296): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.343-9589G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000993 | |||||||
chr13:21001159 | C | T | 74 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(71): Show |
75 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.343-9755G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001159 | |||||||
chr13:21001235 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.343-9831G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001235 | |||||||
chr13:21001244 | T | G | 1 | a0004c0004t0028g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.343-9840A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001244 | |||||||
chr13:21001319 | C | A | 120 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(117): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.343-9915G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001319 | |||||||
chr13:21001379 | C | T | 2 | a0002c0002t0003g0095 a0005c0012t0002g0032 |
2 | HG03017.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.343-9975G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001379 | |||||||
chr13:21001380 | G | A | 76 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(73): Show |
77 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.343-9976C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001380 | |||||||
chr13:21001473 | G | A | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-10069C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001473 | |||||||
chr13:21001487 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.343-10083C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001487 | |||||||
chr13:21001766 | T | A | 72 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(69): Show |
73 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.343-10362A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001766 | |||||||
chr13:21001857 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.343-10453G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001857 | |||||||
chr13:21001873 | C | T | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-10469G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001873 | |||||||
chr13:21001945 | G | T | 10 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-10541C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001945 | |||||||
chr13:21001984 | G | A | 1 | a0001c0001t0013g0205 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.343-10580C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001984 | |||||||
chr13:21001990 | T | C | 173 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(170): Show |
175 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(172): Show |
intron_variant | MODIFIER | c.343-10586A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001990 | |||||||
chr13:21001999 | C | T | 1 | a0002c0014t0018g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.343-10595G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001999 | |||||||
chr13:21002074 | T | C | 299 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(296): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.343-10670A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002074 | |||||||
chr13:21002128 | T | C | 5 | a0002c0002t0011g0036 a0005c0012t0001g0035 a0005c0012t0002g0030 others(2): Show |
5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-10724A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002128 | |||||||
chr13:21002135 | G | A | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0252 |
3 | HG00099.hp1 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.343-10731C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002135 | |||||||
chr13:21002150 | A | T | 174 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(171): Show |
176 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.343-10746T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002150 | |||||||
chr13:21002194 | T | C | 1 | a0009c0033t0001g0302 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.343-10790A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002194 | |||||||
chr13:21002196 | A | G | 1 | a0009c0026t0011g0284 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.343-10792T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002196 | |||||||
chr13:21002197 | G | A | 10 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-10793C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002197 | |||||||
chr13:21002205 | G | A | 123 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(120): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.343-10801C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002205 | |||||||
chr13:21002374 | CT | C | 91 | a0001c0001t0001g0193 a0001c0001t0001g0264 a0001c0001t0001g0273 others(88): Show |
92 | HG00597.hp2 HG00621.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.343-10971delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002374 | |||||||
chr13:21002606 | G | A | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-11202C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002606 | |||||||
chr13:21002813 | C | A | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343-11409G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002813 | |||||||
chr13:21002991 | C | G | 78 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(75): Show |
79 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.343-11587G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002991 | |||||||
chr13:21003212 | GA | G | 72 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(69): Show |
73 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.343-11809delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003212 | |||||||
chr13:21003240 | T | G | 56 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(53): Show |
56 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.343-11836A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003240 | |||||||
chr13:21003397 | G | A | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-11993C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003397 | |||||||
chr13:21003400 | C | T | 72 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(69): Show |
73 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.343-11996G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003400 | |||||||
chr13:21003401 | G | A | 1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.343-11997C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003401 | |||||||
chr13:21003444 | CT | C | 67 | a0001c0001t0001g0219 a0001c0010t0001g0054 a0001c0010t0001g0064 others(64): Show |
68 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.343-12041delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003444 | |||||||
chr13:21003494 | G | A | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-12090C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003494 | |||||||
chr13:21003686 | G | C | 3 | a0001c0001t0002g0225 a0001c0001t0002g0226 a0001c0001t0027g0224 |
3 | HG00741.hp1 HG01106.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.343-12282C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003686 | |||||||
chr13:21003758 | G | T | 1 | a0004c0004t0028g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.343-12354C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003758 | |||||||
chr13:21003846 | G | A | 1 | a0001c0001t0013g0204 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.343-12442C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003846 | |||||||
chr13:21003902 | C | A | 6 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-12498G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003902 | |||||||
chr13:21003968 | G | A | 1 | a0003c0005t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.343-12564C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003968 | |||||||
chr13:21004011 | T | C | 10 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(7): Show |
10 | HG00738.hp1 HG01074.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-12607A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004011 | |||||||
chr13:21004056 | C | T | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-12652G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004056 | |||||||
chr13:21004302 | T | C | 10 | a0003c0005t0002g0066 a0003c0007t0008g0046 a0003c0007t0008g0047 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-12898A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004302 | |||||||
chr13:21004382 | T | C | 3 | a0003c0003t0002g0177 a0003c0003t0002g0178 a0003c0003t0002g0183 |
3 | NA18952.hp2 NA18982.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.343-12978A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004382 | |||||||
chr13:21004394 | A | T | 3 | a0003c0003t0002g0177 a0003c0003t0002g0178 a0003c0003t0002g0183 |
3 | NA18952.hp2 NA18982.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.343-12990T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004394 | |||||||
chr13:21004434 | C | CA | 150 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(147): Show |
151 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(148): Show |
intron_variant | MODIFIER | c.343-13031dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004434 | |||||||
chr13:21004461 | T | A | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-13057A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004461 | |||||||
chr13:21004478 | T | C | 174 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(171): Show |
176 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.343-13074A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004478 | |||||||
chr13:21004488 | A | T | 13 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(10): Show |
13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-13084T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004488 | |||||||
chr13:21004545 | CGT | C | 4 | a0002c0006t0004g0169 a0002c0006t0004g0210 a0002c0006t0004g0211 others(1): Show |
4 | NA18969.hp1 NA18991.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-13143_343-1314 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004545 | |||||||
chr13:21004803 | A | T | 1 | a0003c0005t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.343-13399T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004803 | |||||||
chr13:21005199 | C | G | 2 | a0003c0008t0009g0088 a0009c0033t0001g0302 |
2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.343-13795G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005199 | |||||||
chr13:21005274 | T | C | 2 | a0002c0002t0003g0138 a0002c0002t0003g0145 |
2 | NA19066.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.343-13870A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005274 | |||||||
chr13:21005282 | A | C | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343-13878T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005282 | |||||||
chr13:21005435 | T | C | 10 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-14031A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005435 | |||||||
chr13:21005533 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.343-14129T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005533 | |||||||
chr13:21005592 | G | A | 5 | a0002c0024t0023g0040 a0002c0034t0035g0029 a0003c0008t0009g0088 others(2): Show |
5 | HG00639.hp1 HG01243.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-14188C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005592 | |||||||
chr13:21005805 | A | AT | 14 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0005t0002g0061 others(11): Show |
14 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.343-14402dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005805 | |||||||
chr13:21005805 | A | ATT | 205 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(202): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.343-14402_343-1440 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005805 | |||||||
chr13:21005806 | T | TTTA | 22 | a0001c0001t0006g0182 a0001c0001t0012g0165 a0002c0002t0024g0156 others(19): Show |
22 | HG00597.hp2 HG00639.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.343-14403_343-1440 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005806 | |||||||
chr13:21005806 | T | TTTAA | 8 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(5): Show |
8 | HG01243.hp1 HG01243.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-14403_343-1440 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005806 | |||||||
chr13:21005807 | A | T | 72 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(69): Show |
73 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.343-14403T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005807 | |||||||
chr13:21005808 | A | T | 59 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(56): Show |
60 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.343-14404T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005808 | |||||||
chr13:21005809 | A | T | 1 | a0003c0003t0002g0020 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.343-14405T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005809 | |||||||
chr13:21005818 | A | C | 73 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(70): Show |
74 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-14414T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005818 | |||||||
chr13:21005819 | A | C | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-14415T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005819 | |||||||
chr13:21005841 | A | G | 239 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.343-14437T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005841 | |||||||
chr13:21005853 | C | G | 15 | a0003c0003t0004g0298 a0003c0003t0004g0299 a0003c0008t0009g0292 others(12): Show |
15 | HG01433.hp2 HG02258.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.343-14449G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005853 | |||||||
chr13:21005880 | G | A | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-14476C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005880 | |||||||
chr13:21006040 | G | C | 102 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(99): Show |
103 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.343-14636C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006040 | |||||||
chr13:21006045 | G | A | 1 | a0003c0003t0002g0020 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.343-14641C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006045 | |||||||
chr13:21006069 | A | G | 72 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(69): Show |
73 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.343-14665T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006069 | |||||||
chr13:21006077 | C | T | 1 | a0002c0028t0041g0280 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.343-14673G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006077 | |||||||
chr13:21006078 | G | A | 102 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(99): Show |
103 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.343-14674C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006078 | |||||||
chr13:21006175 | T | C | 3 | a0004c0004t0005g0249 a0004c0004t0005g0288 a0004c0004t0005g0309 |
3 | HG02622.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.343-14771A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006175 | |||||||
chr13:21006207 | G | GA | 98 | a0001c0001t0001g0275 a0001c0001t0006g0182 a0001c0011t0001g0001 others(95): Show |
100 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.343-14804dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006207 | |||||||
chr13:21006378 | A | T | 1 | a0001c0001t0001g0198 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.343-14974T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006378 | |||||||
chr13:21006392 | A | C | 1 | a0003c0005t0002g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.343-14988T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006392 | |||||||
chr13:21006540 | T | C | 13 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(10): Show |
13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-15136A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006540 | |||||||
chr13:21006575 | T | A | 4 | a0002c0002t0010g0279 a0002c0028t0041g0280 a0005c0016t0014g0037 others(1): Show |
4 | HG02965.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-15171A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006575 | |||||||
chr13:21006723 | C | T | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-15319G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006723 | |||||||
chr13:21006823 | C | T | 55 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(52): Show |
55 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.343-15419G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006823 | |||||||
chr13:21006984 | G | C | 72 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(69): Show |
73 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.343-15580C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006984 | |||||||
chr13:21007134 | T | C | 3 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 |
3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.343-15730A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007134 | |||||||
chr13:21007281 | C | T | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-15877G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007281 | |||||||
chr13:21007287 | T | C | 7 | a0003c0009t0008g0307 a0003c0009t0009g0306 a0003c0009t0016g0305 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.343-15883A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007287 | |||||||
chr13:21007300 | A | G | 174 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(171): Show |
176 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.343-15896T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007300 | |||||||
chr13:21007352 | G | A | 1 | a0002c0027t0039g0114 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.343-15948C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007352 | |||||||
chr13:21007373 | A | T | 1 | a0002c0017t0011g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.343-15969T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007373 | |||||||
chr13:21007509 | GAGTAGTT others(218): Show |
G | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-16330_343-1610 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007509 | |||||||
chr13:21007513 | A | C | 6 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-16109T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007513 | |||||||
chr13:21007531 | G | GAT | 26 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(23): Show |
26 | HG00621.hp2 HG00741.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.343-16129_343-1612 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007531 | |||||||
chr13:21007531 | GAT | G | 13 | a0002c0028t0041g0280 a0003c0003t0004g0257 a0003c0003t0025g0285 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-16129_343-1612 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007531 | |||||||
chr13:21007531 | GATATATA others(199): Show |
G | 1 | a0004c0004t0028g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.343-16333_343-1612 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007531 | |||||||
chr13:21007532 | ATATATAT others(197): Show |
A | 1 | a0002c0034t0035g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.343-16332_343-1612 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007532 | |||||||
chr13:21007533 | T | G | 100 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(97): Show |
101 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.343-16129A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007533 | |||||||
chr13:21007536 | ATATATAT others(193): Show |
A | 1 | a0009c0033t0001g0302 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.343-16332_343-1613 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007536 | |||||||
chr13:21007538 | ATATATAG others(191): Show |
A | 1 | a0002c0024t0023g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.343-16332_343-1613 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007538 | |||||||
chr13:21007540 | ATATAGTA others(176): Show |
A | 72 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(69): Show |
73 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.343-16319_343-1613 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007540 | |||||||
chr13:21007542 | ATAGTATA others(174): Show |
A | 15 | a0002c0002t0011g0036 a0002c0006t0004g0014 a0002c0006t0004g0015 others(12): Show |
15 | HG00735.hp1 HG01358.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.343-16319_343-1613 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007542 | |||||||
chr13:21007543 | T | G | 2 | a0001c0022t0004g0010 a0002c0002t0010g0279 |
2 | HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16139A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007543 | |||||||
chr13:21007544 | A | T | 2 | a0001c0022t0004g0010 a0002c0002t0010g0279 |
2 | HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16140T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007544 | |||||||
chr13:21007544 | AG | A | 9 | a0002c0006t0004g0164 a0002c0006t0004g0208 a0002c0014t0018g0041 others(6): Show |
9 | HG00597.hp2 HG01243.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-16141delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007544 | |||||||
chr13:21007544 | AGTATATA others(172): Show |
A | 1 | a0005c0012t0002g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.343-16319_343-1614 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007544 | |||||||
chr13:21007545 | G | A | 3 | a0002c0002t0010g0279 a0004c0004t0005g0249 a0004c0004t0005g0288 |
3 | HG02976.hp1 HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16141C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | |||||||
chr13:21007545 | G | GTA | 15 | a0001c0001t0001g0196 a0001c0001t0001g0206 a0001c0001t0001g0219 others(12): Show |
15 | HG00280.hp1 HG00738.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.343-16143_343-1614 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | |||||||
chr13:21007545 | G | GTATA | 13 | a0001c0001t0001g0236 a0001c0001t0001g0252 a0001c0001t0001g0271 others(10): Show |
13 | HG00741.hp1 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-16145_343-1614 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | |||||||
chr13:21007545 | G | GTATATA | 3 | a0001c0010t0001g0065 a0001c0030t0001g0091 a0003c0003t0002g0178 |
3 | HG01099.hp1 NA18982.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.343-16147_343-1614 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | |||||||
chr13:21007545 | G | GTATATAT others(34): Show |
1 | a0003c0003t0001g0234 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.343-16142_343-1614 others(45): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | |||||||
chr13:21007545 | G | T | 31 | a0003c0003t0002g0011 a0003c0003t0002g0013 a0003c0003t0002g0017 others(28): Show |
31 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.343-16141C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | |||||||
chr13:21007545 | GTA | G | 28 | a0001c0001t0001g0192 a0001c0001t0001g0195 a0001c0001t0001g0198 others(25): Show |
28 | HG00280.hp2 HG00639.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.343-16143_343-1614 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | |||||||
chr13:21007545 | GTATA | G | 16 | a0001c0001t0001g0181 a0001c0001t0001g0193 a0001c0001t0001g0200 others(13): Show |
16 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(13): Show |
intron_variant | MODIFIER | c.343-16145_343-1614 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | |||||||
chr13:21007545 | GTATATAT others(3): Show |
G | 1 | a0001c0001t0002g0216 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.343-16151_343-1614 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | |||||||
chr13:21007545 | GTATATAT others(5): Show |
G | 1 | a0001c0001t0022g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.343-16153_343-1614 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | |||||||
chr13:21007545 | GTATATAT others(9): Show |
G | 1 | a0001c0001t0001g0176 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.343-16157_343-1614 others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | |||||||
chr13:21007546 | T | A | 31 | a0003c0003t0002g0011 a0003c0003t0002g0013 a0003c0003t0002g0017 others(28): Show |
31 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.343-16142A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007546 | |||||||
chr13:21007547 | A | C | 2 | a0003c0005t0012g0079 a0003c0007t0008g0049 |
2 | HG01175.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.343-16143T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007547 | |||||||
chr13:21007547 | A | G | 35 | a0001c0001t0006g0168 a0001c0001t0006g0191 a0001c0001t0012g0165 others(32): Show |
35 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.343-16143T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007547 | |||||||
chr13:21007549 | A | ATATATAT others(18): Show |
1 | a0003c0003t0002g0170 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.343-16146_343-1614 others(29): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007549 | |||||||
chr13:21007549 | A | ATATATAT others(43): Show |
1 | a0001c0001t0001g0245 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.343-16146_343-1614 others(54): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007549 | |||||||
chr13:21007549 | A | G | 4 | a0001c0001t0003g0161 a0001c0001t0029g0189 a0001c0031t0006g0185 others(1): Show |
4 | HG02074.hp1 HG02083.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16145T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007549 | |||||||
chr13:21007551 | A | G | 6 | a0001c0001t0004g0274 a0001c0001t0006g0182 a0001c0001t0006g0184 others(3): Show |
6 | HG00423.hp1 HG02071.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-16147T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007551 | |||||||
chr13:21007553 | A | ATAC | 22 | a0001c0010t0001g0064 a0002c0017t0006g0007 a0003c0003t0002g0020 others(19): Show |
22 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.343-16150_343-1614 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007553 | |||||||
chr13:21007553 | A | G | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343-16149T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007553 | |||||||
chr13:21007553 | ATATATAT others(181): Show |
A | 1 | a0002c0017t0011g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.343-16337_343-1615 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007553 | |||||||
chr13:21007555 | A | AC | 5 | a0001c0010t0001g0054 a0001c0010t0015g0006 a0002c0028t0041g0280 others(2): Show |
5 | HG00741.hp2 HG02602.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16152_343-1615 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007555 | |||||||
chr13:21007555 | A | AG | 5 | a0002c0006t0004g0164 a0002c0006t0004g0208 a0002c0014t0018g0041 others(2): Show |
5 | HG00597.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16152_343-1615 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007555 | |||||||
chr13:21007555 | A | ATATATAT others(12): Show |
1 | a0003c0003t0002g0229 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.343-16152_343-1615 others(23): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007555 | |||||||
chr13:21007557 | A | AG | 3 | a0004c0004t0005g0249 a0004c0004t0005g0288 a0004c0015t0018g0044 |
3 | HG02976.hp1 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.343-16154_343-1615 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007557 | |||||||
chr13:21007557 | A | C | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16153T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007557 | |||||||
chr13:21007557 | ATAT | A | 28 | a0003c0003t0002g0011 a0003c0003t0002g0013 a0003c0003t0002g0017 others(25): Show |
28 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.343-16156_343-1615 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007557 | |||||||
chr13:21007559 | A | AG | 10 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.343-16156_343-1615 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007559 | |||||||
chr13:21007559 | ATATATAT others(101): Show |
A | 1 | a0003c0036t0009g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.343-16263_343-1615 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007559 | |||||||
chr13:21007561 | A | ATATATAT others(4): Show |
1 | a0003c0003t0004g0298 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.343-16158_343-1615 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007561 | |||||||
chr13:21007561 | A | ATATATAT others(31): Show |
1 | a0003c0003t0004g0299 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.343-16158_343-1615 others(42): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007561 | |||||||
chr13:21007561 | A | C | 27 | a0003c0003t0002g0011 a0003c0003t0002g0013 a0003c0003t0002g0017 others(24): Show |
27 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.343-16157T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007561 | |||||||
chr13:21007561 | A | G | 1 | a0003c0005t0002g0045 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.343-16157T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007561 | |||||||
chr13:21007563 | A | AC | 22 | a0001c0010t0001g0064 a0002c0017t0006g0007 a0003c0003t0002g0020 others(19): Show |
22 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.343-16160_343-1615 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007563 | |||||||
chr13:21007563 | A | G | 2 | a0004c0019t0020g0303 a0004c0019t0020g0304 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.343-16159T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007563 | |||||||
chr13:21007565 | A | AC | 4 | a0001c0010t0001g0054 a0001c0010t0015g0006 a0003c0005t0002g0039 others(1): Show |
4 | HG00741.hp2 HG02602.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16162_343-1616 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007565 | |||||||
chr13:21007565 | ATATATAT others(111): Show |
A | 1 | a0004c0015t0018g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.343-16279_343-1616 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007565 | |||||||
chr13:21007566 | T | C | 1 | a0003c0005t0004g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.343-16162A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007566 | |||||||
chr13:21007567 | A | ATATAGTA others(23): Show |
1 | a0004c0004t0019g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.343-16164_343-1616 others(34): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007567 | |||||||
chr13:21007567 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0201 |
2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.343-16163T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007567 | |||||||
chr13:21007569 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0201 |
2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.343-16165T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007569 | |||||||
chr13:21007571 | AT | A | 28 | a0003c0003t0002g0011 a0003c0003t0002g0013 a0003c0003t0002g0017 others(25): Show |
28 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.343-16168delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007571 | |||||||
chr13:21007573 | A | ATATATAT others(4): Show |
1 | a0001c0001t0006g0168 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.343-16170_343-1616 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | |||||||
chr13:21007573 | A | ATATATAT others(6): Show |
1 | a0001c0001t0006g0191 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.343-16170_343-1616 others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | |||||||
chr13:21007573 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0218 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.343-16170_343-1616 others(21): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | |||||||
chr13:21007573 | A | ATATATAT others(49): Show |
1 | a0001c0001t0010g0112 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.343-16170_343-1616 others(60): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | |||||||
chr13:21007573 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0221 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.343-16170_343-1616 others(25): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | |||||||
chr13:21007573 | A | C | 28 | a0003c0003t0002g0011 a0003c0003t0002g0013 a0003c0003t0002g0017 others(25): Show |
28 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.343-16169T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | |||||||
chr13:21007573 | A | G | 2 | a0004c0004t0001g0300 a0004c0004t0001g0301 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-16169T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | |||||||
chr13:21007573 | AT | A | 9 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-16170delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | |||||||
chr13:21007573 | ATATATAT others(181): Show |
A | 1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.343-16357_343-1617 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | |||||||
chr13:21007575 | A | G | 9 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-16171T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007575 | |||||||
chr13:21007575 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0244 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.343-16184_343-1617 others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007575 | |||||||
chr13:21007575 | ATATATAT others(154): Show |
A | 1 | a0002c0014t0018g0042 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.343-16332_343-1617 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007575 | |||||||
chr13:21007577 | A | AC | 22 | a0001c0010t0001g0064 a0002c0017t0006g0007 a0003c0003t0002g0020 others(19): Show |
22 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.343-16174_343-1617 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007577 | |||||||
chr13:21007577 | A | C | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16173T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007577 | |||||||
chr13:21007577 | ATATATAT others(152): Show |
A | 2 | a0002c0014t0018g0041 a0002c0014t0038g0043 |
2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.343-16332_343-1617 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007577 | |||||||
chr13:21007579 | ATATATAT others(22): Show |
A | 1 | a0001c0010t0001g0054 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.343-16204_343-1617 others(33): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007579 | |||||||
chr13:21007579 | ATATATAT others(85): Show |
A | 1 | a0001c0010t0015g0006 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.343-16267_343-1617 others(96): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007579 | |||||||
chr13:21007579 | ATATATAT others(102): Show |
A | 2 | a0003c0005t0002g0039 a0003c0005t0002g0052 |
2 | HG00741.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.343-16284_343-1617 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007579 | |||||||
chr13:21007583 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.343-16179T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007583 | |||||||
chr13:21007585 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.343-16181T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007585 | |||||||
chr13:21007585 | ATAGTATA others(170): Show |
A | 2 | a0002c0006t0004g0164 a0002c0006t0004g0208 |
2 | HG00597.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.343-16358_343-1618 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007585 | |||||||
chr13:21007586 | T | G | 4 | a0001c0001t0001g0092 a0001c0001t0001g0180 a0001c0001t0001g0201 others(1): Show |
4 | HG00423.hp2 HG02015.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16182A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007586 | |||||||
chr13:21007587 | A | AGT | 5 | a0001c0001t0006g0168 a0001c0001t0006g0191 a0004c0004t0005g0249 others(2): Show |
5 | HG02622.hp2 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16185_343-1618 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007587 | |||||||
chr13:21007587 | A | ATAGT | 3 | a0001c0001t0047g0100 a0004c0004t0030g0293 a0004c0035t0009g0295 |
3 | HG03209.hp2 HG03540.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.343-16184_343-1618 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007587 | |||||||
chr13:21007587 | A | ATATATAG others(3): Show |
1 | a0003c0008t0009g0292 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.343-16184_343-1618 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007587 | |||||||
chr13:21007587 | A | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0180 a0001c0001t0001g0201 others(1): Show |
4 | HG00423.hp2 HG02015.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16183T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007587 | |||||||
chr13:21007587 | AG | A | 5 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0010g0163 others(2): Show |
5 | HG00597.hp1 HG02723.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16184delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007587 | |||||||
chr13:21007588 | G | A | 8 | a0001c0001t0001g0180 a0001c0001t0001g0231 a0001c0001t0010g0162 others(5): Show |
8 | HG00423.hp2 HG01433.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-16184C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007588 | |||||||
chr13:21007588 | G | C | 31 | a0003c0003t0002g0011 a0003c0003t0002g0013 a0003c0003t0002g0017 others(28): Show |
31 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.343-16184C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007588 | |||||||
chr13:21007590 | A | G | 3 | a0004c0004t0001g0300 a0004c0004t0001g0301 a0004c0004t0005g0255 |
3 | HG02683.hp2 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-16186T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007590 | |||||||
chr13:21007596 | ATATATAG others(4): Show |
A | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343-16203_343-1619 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007596 | |||||||
chr13:21007598 | ATATAGTG others(1): Show |
A | 25 | a0003c0003t0002g0011 a0003c0003t0002g0013 a0003c0003t0002g0017 others(22): Show |
25 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.343-16202_343-1619 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007598 | |||||||
chr13:21007600 | ATAGTGTG others(3): Show |
A | 19 | a0001c0010t0001g0064 a0002c0017t0006g0007 a0003c0003t0002g0020 others(16): Show |
19 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.343-16206_343-1619 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007600 | |||||||
chr13:21007600 | ATAGTGTG others(62): Show |
A | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-16265_343-1619 others(73): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007600 | |||||||
chr13:21007600 | ATAGTGTG others(81): Show |
A | 2 | a0003c0003t0002g0188 a0003c0005t0015g0071 |
2 | HG03831.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.343-16284_343-1619 others(92): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007600 | |||||||
chr13:21007602 | AGT | A | 10 | a0001c0001t0001g0198 a0001c0001t0001g0245 a0001c0001t0001g0252 others(7): Show |
10 | HG01071.hp1 HG01361.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.343-16200_343-1619 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007602 | |||||||
chr13:21007602 | AGTGTGTA others(41): Show |
A | 2 | a0003c0009t0008g0307 a0003c0009t0032g0287 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.343-16246_343-1619 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007602 | |||||||
chr13:21007603 | G | T | 13 | a0001c0001t0001g0092 a0001c0001t0001g0201 a0001c0001t0002g0002 others(10): Show |
13 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-16199C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007603 | |||||||
chr13:21007603 | GTGTGTA | G | 6 | a0003c0003t0025g0285 a0003c0008t0046g0286 a0003c0009t0009g0306 others(3): Show |
6 | HG02055.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-16205_343-1620 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007603 | |||||||
chr13:21007603 | GTGTGTAT others(79): Show |
G | 1 | a0003c0005t0002g0066 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.343-16285_343-1620 others(90): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007603 | |||||||
chr13:21007604 | T | A | 13 | a0001c0001t0001g0092 a0001c0001t0001g0201 a0001c0001t0002g0002 others(10): Show |
13 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-16200A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007604 | |||||||
chr13:21007605 | G | T | 1 | a0001c0001t0002g0002 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.343-16201C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007605 | |||||||
chr13:21007606 | T | A | 1 | a0001c0001t0002g0002 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.343-16202A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007606 | |||||||
chr13:21007607 | G | A | 114 | a0001c0001t0001g0090 a0001c0001t0001g0176 a0001c0001t0001g0180 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.343-16203C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007607 | |||||||
chr13:21007609 | A | C | 1 | a0001c0010t0001g0054 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.343-16205T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007609 | |||||||
chr13:21007609 | A | G | 5 | a0001c0001t0001g0092 a0001c0001t0001g0201 a0004c0004t0005g0249 others(2): Show |
5 | HG02622.hp2 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16205T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007609 | |||||||
chr13:21007611 | A | C | 17 | a0001c0010t0001g0064 a0002c0017t0006g0007 a0003c0003t0007g0310 others(14): Show |
17 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.343-16207T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007611 | |||||||
chr13:21007611 | A | G | 2 | a0003c0003t0002g0020 a0003c0007t0016g0060 |
2 | HG03704.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.343-16207T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007611 | |||||||
chr13:21007619 | ATAGT | A | 26 | a0003c0003t0002g0011 a0003c0003t0002g0013 a0003c0003t0002g0017 others(23): Show |
26 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.343-16219_343-1621 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007619 | |||||||
chr13:21007619 | ATAGTGTA others(81): Show |
A | 1 | a0003c0003t0004g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.343-16303_343-1621 others(92): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007619 | |||||||
chr13:21007620 | T | G | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16216A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007620 | |||||||
chr13:21007621 | A | T | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16217T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007621 | |||||||
chr13:21007622 | G | A | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16218C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007622 | |||||||
chr13:21007622 | G | C | 1 | a0003c0003t0025g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.343-16218C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007622 | |||||||
chr13:21007622 | G | T | 1 | a0004c0004t0030g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.343-16218C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007622 | |||||||
chr13:21007622 | GTGTATAT others(79): Show |
G | 5 | a0003c0008t0046g0286 a0003c0009t0009g0306 a0003c0009t0016g0305 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16304_343-1621 others(90): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007622 | |||||||
chr13:21007623 | T | A | 1 | a0004c0004t0030g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.343-16219A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007623 | |||||||
chr13:21007624 | G | A | 31 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0001g0065 others(28): Show |
31 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.343-16220C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007624 | |||||||
chr13:21007624 | G | C | 9 | a0003c0003t0002g0253 a0003c0005t0002g0045 a0003c0005t0002g0069 others(6): Show |
9 | HG01167.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-16220C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007624 | |||||||
chr13:21007624 | GTA | G | 3 | a0003c0003t0004g0298 a0003c0003t0004g0299 a0003c0008t0009g0292 |
3 | HG03225.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.343-16222_343-1622 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007624 | |||||||
chr13:21007626 | A | G | 13 | a0001c0001t0001g0092 a0001c0001t0001g0201 a0001c0001t0001g0272 others(10): Show |
13 | HG02004.hp1 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-16222T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007626 | |||||||
chr13:21007628 | A | G | 1 | a0004c0004t0030g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.343-16224T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007628 | |||||||
chr13:21007630 | A | ATATATAG others(21): Show |
1 | a0001c0010t0001g0065 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.343-16227_343-1622 others(32): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007630 | |||||||
chr13:21007630 | A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0002 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.343-16227_343-1622 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007630 | |||||||
chr13:21007630 | A | ATATATAT others(6): Show |
1 | a0001c0001t0010g0163 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.343-16227_343-1622 others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007630 | |||||||
chr13:21007632 | A | AG | 25 | a0001c0010t0001g0064 a0002c0017t0006g0007 a0003c0003t0002g0020 others(22): Show |
25 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.343-16229_343-1622 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | |||||||
chr13:21007632 | A | ATATATAG others(4): Show |
5 | a0001c0001t0001g0180 a0001c0001t0001g0207 a0001c0001t0001g0247 others(2): Show |
5 | HG00099.hp1 HG00099.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16229_343-1622 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | |||||||
chr13:21007632 | A | ATATATAG others(21): Show |
1 | a0001c0001t0001g0252 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.343-16229_343-1622 others(32): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | |||||||
chr13:21007632 | A | ATATATAT others(27): Show |
1 | a0004c0004t0019g0290 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.343-16229_343-1622 others(38): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | |||||||
chr13:21007632 | A | ATATATAT others(6): Show |
8 | a0001c0001t0001g0193 a0001c0001t0001g0243 a0001c0001t0001g0278 others(5): Show |
8 | HG00639.hp2 HG01358.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-16229_343-1622 others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | |||||||
chr13:21007632 | A | ATATATAT others(8): Show |
1 | a0004c0004t0019g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.343-16229_343-1622 others(19): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | |||||||
chr13:21007632 | A | ATATATAT others(25): Show |
1 | a0003c0008t0009g0294 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.343-16229_343-1622 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | |||||||
chr13:21007634 | A | AG | 24 | a0003c0003t0002g0013 a0003c0003t0002g0019 a0003c0003t0002g0021 others(21): Show |
24 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.343-16231_343-1623 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007634 | |||||||
chr13:21007634 | A | ATATATAG others(4): Show |
13 | a0001c0001t0001g0213 a0001c0001t0001g0272 a0001c0001t0003g0161 others(10): Show |
13 | HG00423.hp1 HG02004.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-16231_343-1623 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007634 | |||||||
chr13:21007636 | ATATATAT others(7): Show |
A | 1 | a0003c0003t0025g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.343-16246_343-1623 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007636 | |||||||
chr13:21007638 | ATATATAG others(1): Show |
A | 8 | a0001c0001t0001g0277 a0001c0001t0002g0203 a0001c0001t0047g0100 others(5): Show |
8 | HG01099.hp1 HG02056.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-16242_343-1623 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007638 | |||||||
chr13:21007640 | ATATAGT | A | 84 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(81): Show |
84 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.343-16242_343-1623 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007640 | |||||||
chr13:21007642 | ATAGT | A | 3 | a0001c0001t0001g0245 a0004c0004t0030g0293 a0004c0035t0009g0295 |
3 | HG03209.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.343-16242_343-1623 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007642 | |||||||
chr13:21007644 | AGTGTGT | A | 43 | a0001c0010t0001g0064 a0003c0003t0002g0013 a0003c0003t0002g0019 others(40): Show |
43 | HG00621.hp2 HG00642.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.343-16246_343-1624 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007644 | |||||||
chr13:21007645 | G | T | 24 | a0001c0001t0001g0213 a0001c0001t0001g0252 a0001c0001t0002g0002 others(21): Show |
24 | HG00423.hp1 HG01071.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.343-16241C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007645 | |||||||
chr13:21007645 | GTGTGTGT others(56): Show |
G | 2 | a0002c0017t0006g0007 a0003c0005t0015g0008 |
2 | NA18951.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.343-16304_343-1624 others(67): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007645 | |||||||
chr13:21007646 | T | A | 24 | a0001c0001t0001g0213 a0001c0001t0001g0252 a0001c0001t0002g0002 others(21): Show |
24 | HG00423.hp1 HG01071.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.343-16242A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007646 | |||||||
chr13:21007647 | G | A | 1 | a0004c0019t0020g0303 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.343-16243C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007647 | |||||||
chr13:21007647 | G | T | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16243C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007647 | |||||||
chr13:21007648 | T | A | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16244A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007648 | |||||||
chr13:21007649 | G | A | 5 | a0002c0002t0010g0279 a0002c0028t0041g0280 a0003c0032t0016g0313 others(2): Show |
5 | HG01243.hp1 HG02965.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16245C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007649 | |||||||
chr13:21007649 | G | T | 2 | a0003c0005t0001g0085 a0003c0005t0002g0058 |
2 | HG03453.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.343-16245C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007649 | |||||||
chr13:21007650 | T | A | 2 | a0003c0005t0001g0085 a0003c0005t0002g0058 |
2 | HG03453.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.343-16246A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007650 | |||||||
chr13:21007651 | G | A | 22 | a0001c0001t0001g0180 a0001c0001t0001g0193 a0001c0001t0001g0207 others(19): Show |
22 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.343-16247C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007651 | |||||||
chr13:21007662 | T | C | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16258A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007662 | |||||||
chr13:21007663 | AGTGT | A | 20 | a0001c0010t0001g0064 a0003c0003t0002g0020 a0003c0003t0007g0310 others(17): Show |
20 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.343-16263_343-1626 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007663 | |||||||
chr13:21007664 | G | T | 2 | a0004c0004t0001g0300 a0004c0004t0001g0301 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-16260C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007664 | |||||||
chr13:21007664 | GTGTGTA | G | 27 | a0001c0010t0001g0054 a0003c0003t0002g0011 a0003c0003t0002g0013 others(24): Show |
27 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.343-16266_343-1626 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007664 | |||||||
chr13:21007664 | GTGTGTAT others(1): Show |
G | 4 | a0002c0002t0010g0279 a0002c0028t0041g0280 a0008c0018t0010g0067 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16268_343-1626 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007664 | |||||||
chr13:21007664 | GTGTGTAT others(37): Show |
G | 2 | a0003c0005t0002g0050 a0003c0005t0002g0051 |
2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.343-16304_343-1626 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007664 | |||||||
chr13:21007665 | T | A | 2 | a0004c0004t0001g0300 a0004c0004t0001g0301 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-16261A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007665 | |||||||
chr13:21007666 | G | A | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16262C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007666 | |||||||
chr13:21007666 | G | GTATATAT others(31): Show |
1 | a0004c0035t0009g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.343-16263_343-1626 others(42): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007666 | |||||||
chr13:21007668 | G | A | 9 | a0001c0001t0001g0092 a0001c0001t0001g0201 a0001c0001t0001g0252 others(6): Show |
9 | HG01071.hp1 HG01433.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-16264C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007668 | |||||||
chr13:21007668 | G | C | 1 | a0003c0003t0025g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.343-16264C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007668 | |||||||
chr13:21007670 | A | C | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-16266T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007670 | |||||||
chr13:21007672 | A | C | 1 | a0001c0010t0015g0006 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.343-16268T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007672 | |||||||
chr13:21007681 | T | G | 28 | a0001c0001t0001g0180 a0001c0001t0001g0193 a0001c0001t0001g0207 others(25): Show |
28 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.343-16277A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007681 | |||||||
chr13:21007681 | T | TGTGTATA others(19): Show |
1 | a0001c0001t0001g0235 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.343-16278_343-1627 others(30): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007681 | |||||||
chr13:21007682 | A | AGT | 8 | a0001c0001t0001g0264 a0004c0004t0001g0300 a0004c0004t0001g0301 others(5): Show |
8 | HG01255.hp1 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-16280_343-1627 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007682 | |||||||
chr13:21007682 | A | ATGTGTAT others(19): Show |
1 | a0001c0001t0001g0236 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.343-16279_343-1627 others(30): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007682 | |||||||
chr13:21007682 | A | T | 29 | a0001c0001t0001g0180 a0001c0001t0001g0193 a0001c0001t0001g0207 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.343-16278T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007682 | |||||||
chr13:21007682 | AG | A | 8 | a0001c0001t0001g0092 a0001c0001t0001g0201 a0001c0001t0001g0252 others(5): Show |
8 | HG01071.hp1 HG01243.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-16279delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007682 | |||||||
chr13:21007683 | G | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | NA19011.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.343-16279C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | |||||||
chr13:21007683 | G | GTGTGTAT others(14): Show |
1 | a0001c0001t0010g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.343-16280_343-1627 others(25): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | |||||||
chr13:21007683 | G | GTGTGTAT others(16): Show |
1 | a0001c0001t0013g0204 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.343-16280_343-1627 others(27): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | |||||||
chr13:21007683 | G | GTGTGTAT others(16): Show |
6 | a0001c0001t0001g0176 a0001c0001t0001g0181 a0001c0001t0001g0209 others(3): Show |
6 | HG01515.hp2 HG02280.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-16280_343-1627 others(27): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | |||||||
chr13:21007683 | G | GTGTGTAT others(18): Show |
7 | a0001c0001t0001g0200 a0001c0001t0001g0275 a0001c0001t0002g0216 others(4): Show |
7 | HG00642.hp1 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.343-16280_343-1627 others(29): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | |||||||
chr13:21007683 | G | GTGTGTAT others(20): Show |
6 | a0004c0004t0005g0197 a0004c0004t0005g0227 a0004c0004t0005g0228 others(3): Show |
6 | HG02735.hp2 HG02738.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-16280_343-1627 others(31): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | |||||||
chr13:21007683 | G | GTGTGTAT others(18): Show |
1 | a0001c0001t0001g0245 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.343-16280_343-1627 others(29): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | |||||||
chr13:21007683 | GTA | G | 10 | a0001c0010t0001g0064 a0003c0003t0007g0310 a0003c0003t0007g0311 others(7): Show |
10 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-16281_343-1628 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | |||||||
chr13:21007683 | GTATATAT others(18): Show |
G | 1 | a0003c0005t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.343-16304_343-1628 others(29): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | |||||||
chr13:21007685 | A | G | 71 | a0001c0001t0001g0090 a0001c0001t0001g0180 a0001c0001t0001g0192 others(68): Show |
72 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.343-16281T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007685 | |||||||
chr13:21007687 | A | G | 64 | a0001c0001t0001g0090 a0001c0001t0001g0192 a0001c0001t0001g0195 others(61): Show |
65 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.343-16283T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007687 | |||||||
chr13:21007687 | AT | A | 3 | a0001c0001t0001g0201 a0004c0004t0005g0249 a0004c0004t0005g0309 |
3 | HG02622.hp2 HG03041.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.343-16284delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007687 | |||||||
chr13:21007689 | A | C | 4 | a0003c0003t0002g0188 a0003c0005t0002g0039 a0003c0005t0002g0052 others(1): Show |
4 | HG00741.hp2 HG03831.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-16285T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007689 | |||||||
chr13:21007689 | A | G | 5 | a0001c0001t0001g0201 a0001c0001t0001g0252 a0004c0004t0005g0249 others(2): Show |
5 | HG01071.hp1 HG02622.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16285T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007689 | |||||||
chr13:21007689 | ATATATAT others(40): Show |
A | 2 | a0003c0005t0002g0276 a0003c0005t0033g0077 |
2 | HG03834.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.343-16332_343-1628 others(51): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007689 | |||||||
chr13:21007691 | A | G | 4 | a0001c0001t0001g0092 a0001c0001t0001g0201 a0004c0004t0005g0249 others(1): Show |
4 | HG02622.hp2 HG03041.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16287T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007691 | |||||||
chr13:21007691 | ATATATAT others(38): Show |
A | 1 | a0003c0005t0002g0062 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.343-16332_343-1628 others(49): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007691 | |||||||
chr13:21007693 | A | AG | 3 | a0002c0002t0010g0279 a0002c0028t0041g0280 a0008c0018t0010g0067 |
3 | HG02572.hp1 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16290_343-1628 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007693 | |||||||
chr13:21007693 | A | ATAGTGTA others(25): Show |
1 | a0001c0001t0001g0220 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.343-16290_343-1628 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007693 | |||||||
chr13:21007693 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.343-16289T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007693 | |||||||
chr13:21007693 | ATATATAG others(9): Show |
A | 1 | a0008c0018t0010g0068 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.343-16305_343-1629 others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007693 | |||||||
chr13:21007695 | A | G | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16291T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007695 | |||||||
chr13:21007695 | ATATAGTA others(3): Show |
A | 1 | a0003c0036t0009g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.343-16301_343-1629 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007695 | |||||||
chr13:21007695 | ATATAGTA others(5): Show |
A | 3 | a0003c0003t0025g0285 a0003c0009t0008g0307 a0003c0009t0032g0287 |
3 | HG02055.hp2 HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.343-16303_343-1629 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007695 | |||||||
chr13:21007697 | ATAGTATG others(3): Show |
A | 24 | a0001c0010t0001g0054 a0003c0003t0002g0013 a0003c0003t0002g0019 others(21): Show |
24 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.343-16303_343-1629 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007697 | |||||||
chr13:21007697 | ATAGTATG others(5): Show |
A | 1 | a0003c0023t0002g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.343-16305_343-1629 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007697 | |||||||
chr13:21007697 | ATAGTATG others(26): Show |
A | 1 | a0003c0005t0002g0058 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.343-16326_343-1629 others(37): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007697 | |||||||
chr13:21007698 | T | C | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16294A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007698 | |||||||
chr13:21007698 | T | G | 2 | a0003c0032t0016g0313 a0004c0019t0020g0303 |
2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.343-16294A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007698 | |||||||
chr13:21007699 | A | AGT | 3 | a0001c0001t0001g0181 a0001c0001t0001g0245 a0001c0001t0002g0216 |
3 | HG01081.hp2 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.343-16297_343-1629 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | AGTGTATA others(24): Show |
1 | a0002c0006t0004g0254 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.343-16296_343-1629 others(35): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | ATAGTGTA others(3): Show |
1 | a0001c0001t0001g0243 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.343-16296_343-1629 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | ATATAGTG others(5): Show |
4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0010g0112 others(1): Show |
4 | HG00099.hp1 NA18998.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-16296_343-1629 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | ATATAGTG others(5): Show |
2 | a0001c0001t0001g0278 a0001c0001t0043g0139 |
2 | NA18983.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.343-16296_343-1629 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | ATATATAG others(3): Show |
1 | a0003c0003t0001g0234 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.343-16296_343-1629 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | ATATATAG others(5): Show |
2 | a0001c0001t0004g0274 a0001c0001t0029g0189 |
2 | HG02083.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.343-16296_343-1629 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | ATATATAG others(7): Show |
2 | a0001c0001t0006g0182 a0001c0001t0012g0165 |
2 | NA18979.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.343-16296_343-1629 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | ATATATAG others(7): Show |
2 | a0001c0001t0001g0272 a0001c0001t0013g0167 |
2 | HG02004.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.343-16296_343-1629 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0193 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.343-16296_343-1629 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | ATATATAT others(7): Show |
5 | a0001c0001t0001g0213 a0001c0001t0006g0184 a0001c0001t0006g0190 others(2): Show |
5 | HG00423.hp1 HG02071.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16296_343-1629 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | ATATATAT others(9): Show |
2 | a0001c0001t0003g0161 a0001c0001t0006g0168 |
2 | HG02074.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.343-16296_343-1629 others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | ATATATAT others(7): Show |
1 | a0004c0004t0005g0004 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.343-16296_343-1629 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0207 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.343-16296_343-1629 others(24): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | ATATATAT others(9): Show |
1 | a0004c0004t0005g0256 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-16296_343-1629 others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | A | T | 2 | a0003c0032t0016g0313 a0004c0019t0020g0303 |
2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.343-16295T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | AG | A | 6 | a0001c0001t0001g0220 a0002c0002t0010g0279 a0002c0028t0041g0280 others(3): Show |
6 | HG02280.hp2 HG02622.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-16296delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007699 | AGTATG | A | 5 | a0001c0001t0001g0092 a0001c0001t0001g0201 a0001c0001t0001g0252 others(2): Show |
5 | HG01071.hp1 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16300_343-1629 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | |||||||
chr13:21007700 | G | A | 25 | a0001c0001t0001g0207 a0001c0001t0001g0213 a0001c0001t0001g0243 others(22): Show |
25 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.343-16296C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | C | 1 | a0001c0010t0015g0006 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.343-16296C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTA | 16 | a0001c0001t0001g0176 a0001c0001t0001g0209 a0001c0001t0001g0235 others(13): Show |
16 | HG01106.hp1 HG01433.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(20): Show |
1 | a0001c0001t0001g0221 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(31): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(22): Show |
4 | a0001c0001t0002g0002 a0001c0001t0002g0166 a0001c0001t0002g0199 others(1): Show |
5 | HG02683.hp1 NA18986.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(33): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(20): Show |
2 | a0003c0003t0002g0172 a0003c0003t0002g0173 |
2 | HG01099.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.343-16297_343-1629 others(31): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(22): Show |
5 | a0001c0001t0001g0222 a0001c0001t0002g0203 a0003c0003t0002g0177 others(2): Show |
5 | HG00597.hp1 NA18952.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(33): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(24): Show |
7 | a0001c0001t0001g0218 a0001c0001t0001g0230 a0001c0001t0001g0237 others(4): Show |
7 | HG01943.hp1 NA18950.hp2 NA18992.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(35): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(26): Show |
2 | a0001c0001t0001g0212 a0001c0001t0001g0219 |
2 | NA18954.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.343-16297_343-1629 others(37): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(28): Show |
1 | a0001c0001t0001g0244 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(39): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(22): Show |
2 | a0001c0001t0001g0261 a0003c0003t0002g0175 |
2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.343-16297_343-1629 others(33): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(24): Show |
1 | a0004c0004t0005g0267 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.343-16297_343-1629 others(35): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(24): Show |
4 | a0001c0001t0001g0260 a0001c0001t0017g0131 a0001c0001t0047g0100 others(1): Show |
4 | HG01928.hp2 NA18946.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(35): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(26): Show |
13 | a0001c0001t0001g0196 a0001c0001t0001g0262 a0001c0001t0001g0264 others(10): Show |
13 | HG01070.hp1 HG01074.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(37): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(28): Show |
1 | a0001c0001t0001g0198 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(39): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(53): Show |
1 | a0001c0001t0001g0215 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(64): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(24): Show |
3 | a0001c0001t0001g0195 a0004c0004t0005g0246 a0004c0004t0005g0259 |
3 | HG01175.hp1 HG01361.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.343-16297_343-1629 others(35): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(26): Show |
1 | a0004c0004t0005g0089 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(37): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(26): Show |
7 | a0001c0001t0001g0192 a0001c0001t0001g0206 a0001c0001t0002g0225 others(4): Show |
7 | HG00280.hp1 HG00438.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(37): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(28): Show |
5 | a0001c0001t0001g0202 a0001c0001t0001g0231 a0001c0001t0001g0277 others(2): Show |
5 | HG00423.hp2 HG02056.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(39): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(30): Show |
2 | a0001c0001t0001g0090 a0001c0030t0001g0091 |
2 | HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.343-16297_343-1629 others(41): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(28): Show |
1 | a0004c0015t0005g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(39): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTATAT others(30): Show |
1 | a0001c0001t0027g0224 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.343-16297_343-1629 others(41): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | GTGTGTAT others(45): Show |
1 | a0001c0001t0001g0180 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(56): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007700 | G | T | 2 | a0004c0004t0001g0300 a0004c0004t0001g0301 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-16296C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | |||||||
chr13:21007701 | T | A | 2 | a0004c0004t0001g0300 a0004c0004t0001g0301 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-16297A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007701 | |||||||
chr13:21007701 | T | TGTATATA others(8): Show |
2 | a0004c0004t0019g0290 a0004c0004t0030g0293 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.343-16298_343-1629 others(19): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007701 | |||||||
chr13:21007702 | A | G | 7 | a0001c0010t0001g0065 a0003c0007t0036g0053 a0004c0004t0001g0300 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.343-16298T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007702 | |||||||
chr13:21007704 | G | A | 147 | a0001c0001t0001g0090 a0001c0001t0001g0176 a0001c0001t0001g0180 others(144): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.343-16300C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007704 | |||||||
chr13:21007705 | T | C | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16301A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007705 | |||||||
chr13:21007706 | A | G | 2 | a0003c0007t0036g0053 a0003c0036t0009g0308 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.343-16302T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007706 | |||||||
chr13:21007708 | A | C | 3 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0009t0032g0287 |
3 | HG02055.hp2 HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.343-16304T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007708 | |||||||
chr13:21007708 | A | G | 25 | a0001c0010t0001g0054 a0003c0003t0002g0013 a0003c0003t0002g0019 others(22): Show |
25 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.343-16304T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007708 | |||||||
chr13:21007710 | A | AG | 8 | a0003c0003t0002g0188 a0003c0005t0002g0039 a0003c0005t0002g0052 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-16307_343-1630 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007710 | |||||||
chr13:21007710 | A | C | 1 | a0003c0023t0002g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.343-16306T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007710 | |||||||
chr13:21007710 | A | G | 1 | a0008c0018t0010g0068 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.343-16306T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007710 | |||||||
chr13:21007712 | A | G | 1 | a0001c0010t0015g0006 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.343-16308T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007712 | |||||||
chr13:21007720 | A | C | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-16316T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007720 | |||||||
chr13:21007720 | A | G | 1 | a0003c0003t0002g0020 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.343-16316T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007720 | |||||||
chr13:21007721 | T | C | 2 | a0001c0001t0001g0219 a0003c0008t0046g0286 |
2 | HG02630.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.343-16317A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007721 | |||||||
chr13:21007721 | TAGTATAT others(24): Show |
T | 10 | a0001c0010t0001g0064 a0003c0003t0007g0310 a0003c0003t0007g0311 others(7): Show |
10 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-16348_343-1631 others(35): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007721 | |||||||
chr13:21007723 | G | A | 1 | a0004c0004t0019g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.343-16319C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007723 | |||||||
chr13:21007723 | G | GTA | 3 | a0002c0017t0006g0007 a0003c0005t0015g0008 a0008c0018t0010g0067 |
3 | HG02572.hp1 NA18951.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.343-16321_343-1632 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007723 | |||||||
chr13:21007723 | G | GTATATAT others(8): Show |
1 | a0008c0018t0010g0068 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.343-16334_343-1632 others(19): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007723 | |||||||
chr13:21007723 | G | GTGTATAT others(18): Show |
2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16320_343-1631 others(29): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007723 | |||||||
chr13:21007725 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.343-16321T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007725 | |||||||
chr13:21007727 | ATATATAT others(2): Show |
A | 5 | a0003c0003t0002g0019 a0003c0005t0002g0073 a0003c0005t0002g0074 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16332_343-1632 others(13): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007727 | |||||||
chr13:21007729 | ATATATAG | A | 18 | a0003c0003t0002g0011 a0003c0003t0002g0017 a0003c0003t0002g0021 others(15): Show |
18 | HG00642.hp2 HG01175.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.343-16332_343-1632 others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007729 | |||||||
chr13:21007731 | A | G | 1 | a0003c0005t0002g0058 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.343-16327T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007731 | |||||||
chr13:21007731 | ATATAG | A | 6 | a0001c0010t0001g0054 a0003c0003t0002g0013 a0003c0005t0001g0085 others(3): Show |
6 | HG01167.hp2 HG01168.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-16332_343-1632 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007731 | |||||||
chr13:21007734 | T | G | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-16330A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007734 | |||||||
chr13:21007735 | A | T | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-16331T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007735 | |||||||
chr13:21007735 | AG | A | 4 | a0001c0022t0004g0010 a0003c0005t0002g0058 a0004c0019t0020g0303 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16332delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007735 | |||||||
chr13:21007736 | G | A | 2 | a0003c0007t0036g0053 a0004c0015t0018g0044 |
2 | HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.343-16332C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007736 | |||||||
chr13:21007736 | G | C | 9 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-16332C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007736 | |||||||
chr13:21007736 | G | T | 1 | a0004c0035t0009g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.343-16332C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007736 | |||||||
chr13:21007736 | GTATA | G | 5 | a0002c0002t0003g0104 a0002c0002t0003g0108 a0002c0002t0003g0122 others(2): Show |
5 | HG01255.hp2 HG02809.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16336_343-1633 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007736 | |||||||
chr13:21007737 | T | A | 1 | a0004c0035t0009g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.343-16333A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007737 | |||||||
chr13:21007737 | T | G | 1 | a0002c0034t0035g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.343-16333A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007737 | |||||||
chr13:21007738 | A | ATATATAT others(6): Show |
1 | a0003c0005t0002g0052 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.343-16335_343-1633 others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007738 | |||||||
chr13:21007738 | A | G | 123 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(120): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.343-16334T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007738 | |||||||
chr13:21007739 | T | G | 1 | a0004c0004t0028g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.343-16335A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007739 | |||||||
chr13:21007740 | A | ATATATAT others(4): Show |
3 | a0003c0003t0002g0188 a0003c0005t0002g0039 a0003c0005t0015g0071 |
3 | HG03831.hp1 NA18992.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.343-16337_343-1633 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007740 | |||||||
chr13:21007740 | A | G | 3 | a0001c0001t0001g0207 a0001c0001t0017g0130 a0004c0004t0021g0251 |
3 | HG01167.hp1 HG02738.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.343-16336T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007740 | |||||||
chr13:21007742 | A | G | 1 | a0002c0017t0011g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.343-16338T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007742 | |||||||
chr13:21007749 | T | TA | 3 | a0003c0009t0008g0307 a0003c0009t0009g0306 a0003c0009t0016g0305 |
3 | HG02622.hp1 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.343-16346dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007749 | |||||||
chr13:21007750 | A | T | 1 | a0003c0005t0002g0078 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.343-16346T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007750 | |||||||
chr13:21007751 | TA | T | 7 | a0001c0010t0001g0054 a0002c0014t0018g0041 a0003c0005t0002g0062 others(4): Show |
7 | HG01168.hp2 HG01175.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-16348delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007751 | |||||||
chr13:21007752 | A | T | 3 | a0003c0005t0002g0045 a0003c0005t0002g0070 a0003c0005t0002g0078 |
3 | HG01167.hp2 HG03942.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.343-16348T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007752 | |||||||
chr13:21007753 | TA | T | 4 | a0003c0003t0002g0013 a0003c0003t0002g0253 a0003c0005t0001g0085 others(1): Show |
4 | HG01258.hp2 HG03453.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-16350delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007753 | |||||||
chr13:21007753 | TATATA | T | 12 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(9): Show |
13 | HG02148.hp2 HG02155.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-16354_343-1635 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007753 | |||||||
chr13:21007754 | A | T | 32 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0002c0014t0018g0041 others(29): Show |
32 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.343-16350T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007754 | |||||||
chr13:21007755 | TA | T | 3 | a0003c0008t0009g0294 a0004c0004t0019g0290 a0004c0004t0030g0293 |
3 | HG01433.hp2 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.343-16352delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007755 | |||||||
chr13:21007755 | TATATA | T | 41 | a0002c0002t0003g0094 a0002c0002t0003g0095 a0002c0002t0003g0096 others(38): Show |
41 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.343-16356_343-1635 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007755 | |||||||
chr13:21007756 | A | ATTTTT | 3 | a0001c0010t0015g0006 a0002c0017t0006g0007 a0003c0005t0015g0008 |
3 | NA18951.hp2 NA18986.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.343-16353_343-1635 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007756 | |||||||
chr13:21007756 | A | T | 45 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0002c0014t0018g0041 others(42): Show |
45 | HG00621.hp2 HG00642.hp2 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.343-16352T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007756 | |||||||
chr13:21007756 | ATATAT | A | 7 | a0002c0002t0003g0098 a0002c0002t0003g0124 a0002c0002t0003g0150 others(4): Show |
7 | HG02602.hp1 NA18612.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-16357_343-1635 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007756 | |||||||
chr13:21007757 | TATA | T | 3 | a0002c0002t0011g0036 a0002c0002t0040g0143 a0005c0012t0001g0035 |
3 | HG00735.hp1 HG02559.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.343-16356_343-1635 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007757 | |||||||
chr13:21007758 | A | AT | 18 | a0001c0001t0001g0090 a0001c0030t0001g0091 a0002c0006t0004g0254 others(15): Show |
18 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.343-16355dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007758 | |||||||
chr13:21007758 | A | T | 63 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(60): Show |
64 | HG00621.hp2 HG00642.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.343-16354T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007758 | |||||||
chr13:21007760 | A | AT | 19 | a0001c0001t0001g0196 a0001c0001t0001g0245 a0001c0001t0001g0247 others(16): Show |
19 | HG00099.hp1 HG00741.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.343-16357dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007760 | |||||||
chr13:21007760 | A | T | 99 | a0001c0001t0001g0090 a0001c0010t0001g0054 a0001c0010t0001g0064 others(96): Show |
101 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.343-16356T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007760 | |||||||
chr13:21007761 | T | TA | 82 | a0001c0001t0001g0092 a0001c0001t0001g0176 a0001c0001t0001g0181 others(79): Show |
83 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.343-16358_343-1635 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007761 | |||||||
chr13:21007761 | T | TAATATAT others(7): Show |
1 | a0003c0036t0009g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.343-16358_343-1635 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007761 | |||||||
chr13:21007761 | T | TATA | 7 | a0001c0001t0001g0215 a0001c0001t0001g0230 a0001c0001t0001g0237 others(4): Show |
7 | HG01081.hp1 NA18945.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-16358_343-1635 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007761 | |||||||
chr13:21007761 | T | TATATA | 3 | a0001c0001t0001g0180 a0005c0016t0014g0037 a0005c0016t0014g0038 |
3 | HG02015.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16358_343-1635 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007761 | |||||||
chr13:21007762 | T | A | 13 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(10): Show |
13 | HG01070.hp1 HG01496.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-16358A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007762 | |||||||
chr13:21007763 | T | A | 15 | a0001c0001t0001g0092 a0001c0001t0001g0207 a0001c0001t0001g0219 others(12): Show |
15 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.343-16359A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007763 | |||||||
chr13:21007764 | T | A | 3 | a0003c0009t0026g0031 a0003c0009t0031g0033 a0003c0032t0016g0313 |
3 | HG02723.hp2 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.343-16360A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007764 | |||||||
chr13:21007765 | T | A | 3 | a0003c0005t0002g0066 a0005c0016t0014g0037 a0005c0016t0014g0038 |
3 | HG03139.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.343-16361A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007765 | |||||||
chr13:21007767 | T | A | 2 | a0003c0005t0002g0066 a0005c0016t0014g0038 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.343-16363A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007767 | |||||||
chr13:21008027 | G | C | 2 | a0002c0034t0035g0029 a0004c0004t0028g0027 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.343-16623C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008027 | |||||||
chr13:21008051 | A | G | 24 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(21): Show |
24 | HG00597.hp2 HG00639.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.343-16647T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008051 | |||||||
chr13:21008190 | GCTA | G | 24 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(21): Show |
24 | HG00597.hp2 HG00639.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.343-16789_343-1678 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008190 | |||||||
chr13:21008305 | T | C | 173 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(170): Show |
175 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(172): Show |
intron_variant | MODIFIER | c.343-16901A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008305 | |||||||
chr13:21008478 | T | C | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-17074A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008478 | |||||||
chr13:21008580 | A | T | 1 | a0001c0001t0001g0244 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.343-17176T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008580 | |||||||
chr13:21008757 | C | A | 9 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(6): Show |
10 | HG00735.hp2 HG02451.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-17353G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008757 | |||||||
chr13:21008781 | C | T | 40 | a0001c0001t0001g0180 a0001c0001t0001g0195 a0001c0001t0001g0196 others(37): Show |
41 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.343-17377G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008781 | |||||||
chr13:21009015 | A | C | 2 | a0003c0005t0002g0066 a0003c0007t0036g0053 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.343-17611T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009015 | |||||||
chr13:21009034 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.343-17630C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009034 | |||||||
chr13:21009094 | C | T | 1 | a0002c0002t0010g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.343-17690G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009094 | |||||||
chr13:21009146 | C | T | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-17742G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009146 | |||||||
chr13:21009193 | A | G | 104 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(101): Show |
105 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.343-17789T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009193 | |||||||
chr13:21009202 | G | A | 307 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(304): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.343-17798C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009202 | |||||||
chr13:21009410 | C | T | 1 | a0003c0003t0002g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.343-18006G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009410 | |||||||
chr13:21009433 | A | G | 102 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(99): Show |
103 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.343-18029T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009433 | |||||||
chr13:21009641 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.343-18237A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009641 | |||||||
chr13:21009705 | G | A | 102 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(99): Show |
103 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.343-18301C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009705 | |||||||
chr13:21009881 | C | T | 1 | a0002c0028t0041g0280 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.343-18477G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009881 | |||||||
chr13:21010027 | C | T | 6 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-18623G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010027 | |||||||
chr13:21010092 | C | T | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-18688G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010092 | |||||||
chr13:21010093 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.343-18689C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010093 | |||||||
chr13:21010177 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.343-18773C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010177 | |||||||
chr13:21010196 | T | TCAAA | 3 | a0001c0010t0001g0054 a0003c0005t0002g0055 a0003c0005t0015g0071 |
3 | HG02071.hp2 HG02602.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.343-18796_343-1879 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010196 | |||||||
chr13:21010196 | T | TCAAACAA others(1): Show |
49 | a0001c0010t0001g0064 a0001c0010t0015g0006 a0002c0017t0006g0007 others(46): Show |
49 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.343-18793_343-1879 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010196 | |||||||
chr13:21010201 | A | AAAAC | 14 | a0001c0001t0003g0161 a0001c0001t0004g0274 a0001c0001t0006g0168 others(11): Show |
14 | HG00423.hp1 HG02055.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.343-18801_343-1879 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | |||||||
chr13:21010201 | A | AAAACAAA others(1): Show |
94 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0252 others(91): Show |
95 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.343-18805_343-1879 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | |||||||
chr13:21010201 | A | AAAACAAA others(5): Show |
102 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(99): Show |
103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.343-18809_343-1879 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | |||||||
chr13:21010201 | A | AAAACAAA others(9): Show |
13 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0221 others(10): Show |
14 | HG00423.hp2 HG00597.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.343-18813_343-1879 others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | |||||||
chr13:21010201 | A | AAACAAAC others(8): Show |
1 | a0001c0001t0002g0225 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.343-18798_343-1879 others(19): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | |||||||
chr13:21010201 | A | ACAAACAA others(2): Show |
17 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(14): Show |
17 | HG00597.hp2 HG00639.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.343-18798_343-1879 others(13): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | |||||||
chr13:21010201 | A | ACAAACAA others(10): Show |
1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.343-18798_343-1879 others(21): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | |||||||
chr13:21010201 | A | C | 55 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(52): Show |
55 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.343-18797T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | |||||||
chr13:21010548 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.343-19144A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010548 | |||||||
chr13:21010727 | G | T | 1 | a0001c0001t0002g0223 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.343-19323C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010727 | |||||||
chr13:21010824 | T | C | 1 | a0003c0005t0004g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.343-19420A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010824 | |||||||
chr13:21011181 | C | T | 1 | a0003c0007t0016g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.343-19777G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011181 | |||||||
chr13:21011182 | T | G | 10 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-19778A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011182 | |||||||
chr13:21011472 | C | G | 1 | a0002c0017t0011g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.343-20068G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011472 | |||||||
chr13:21011652 | T | TAAGCAGC others(12): Show |
2 | a0001c0001t0001g0181 a0001c0001t0001g0209 |
2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.343-20249_343-2024 others(23): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011652 | |||||||
chr13:21011656 | G | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0209 |
2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.343-20252C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011656 | |||||||
chr13:21011845 | C | A | 297 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(294): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.343-20441G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011845 | |||||||
chr13:21011905 | T | G | 72 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(69): Show |
73 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.343-20501A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011905 | |||||||
chr13:21011927 | T | A | 78 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(75): Show |
79 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.343-20523A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011927 | |||||||
chr13:21012207 | A | T | 74 | a0001c0001t0037g0186 a0001c0010t0001g0054 a0001c0010t0001g0064 others(71): Show |
75 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.343-20803T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012207 | |||||||
chr13:21012234 | C | A | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-20830G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012234 | |||||||
chr13:21012275 | G | A | 5 | a0002c0002t0011g0036 a0005c0012t0001g0035 a0005c0012t0002g0030 others(2): Show |
5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-20871C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012275 | |||||||
chr13:21012359 | G | A | 10 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(7): Show |
10 | HG00597.hp1 HG02056.hp2 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.343-20955C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012359 | |||||||
chr13:21012508 | C | T | 307 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(304): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.343-21104G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012508 | |||||||
chr13:21012724 | T | A | 2 | a0003c0008t0009g0088 a0009c0033t0001g0302 |
2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.343-21320A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012724 | |||||||
chr13:21012739 | C | A | 2 | a0004c0004t0001g0300 a0004c0004t0001g0301 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-21335G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012739 | |||||||
chr13:21012744 | C | T | 6 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-21340G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012744 | |||||||
chr13:21012785 | A | ACC | 15 | a0002c0002t0003g0103 a0002c0006t0004g0014 a0002c0006t0004g0015 others(12): Show |
15 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.343-21383_343-2138 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012785 | |||||||
chr13:21012785 | AC | A | 79 | a0001c0001t0001g0180 a0001c0001t0001g0218 a0001c0001t0001g0221 others(76): Show |
80 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.343-21382delG | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012785 | |||||||
chr13:21012788 | C | A | 72 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(69): Show |
73 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.343-21384G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012788 | |||||||
chr13:21012795 | C | G | 1 | a0002c0002t0003g0108 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.343-21391G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012795 | |||||||
chr13:21012995 | G | A | 1 | a0002c0002t0003g0101 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.343-21591C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012995 | |||||||
chr13:21013223 | G | T | 5 | a0002c0002t0011g0036 a0005c0012t0001g0035 a0005c0012t0002g0030 others(2): Show |
5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-21819C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013223 | |||||||
chr13:21013224 | C | A | 5 | a0002c0002t0011g0036 a0005c0012t0001g0035 a0005c0012t0002g0030 others(2): Show |
5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-21820G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013224 | |||||||
chr13:21013327 | C | T | 1 | a0003c0003t0002g0188 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.343-21923G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013327 | |||||||
chr13:21013328 | G | A | 73 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(70): Show |
74 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-21924C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013328 | |||||||
chr13:21013466 | G | C | 2 | a0002c0002t0003g0157 a0002c0002t0003g0158 |
2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.343-22062C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013466 | |||||||
chr13:21013474 | C | T | 5 | a0002c0024t0023g0040 a0002c0034t0035g0029 a0003c0008t0009g0088 others(2): Show |
5 | HG00639.hp1 HG01243.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-22070G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013474 | |||||||
chr13:21013742 | G | A | 5 | a0002c0024t0023g0040 a0002c0034t0035g0029 a0003c0008t0009g0088 others(2): Show |
5 | HG00639.hp1 HG01243.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-22338C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013742 | |||||||
chr13:21013788 | A | G | 10 | a0003c0005t0002g0066 a0003c0007t0008g0046 a0003c0007t0008g0047 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-22384T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013788 | |||||||
chr13:21013791 | C | T | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-22387G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013791 | |||||||
chr13:21013853 | C | T | 1 | a0003c0007t0016g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.343-22449G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013853 | |||||||
chr13:21013941 | A | G | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-22537T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013941 | |||||||
chr13:21013956 | G | A | 14 | a0001c0001t0006g0232 a0002c0006t0004g0014 a0002c0006t0004g0015 others(11): Show |
14 | HG00423.hp1 HG00597.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.343-22552C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013956 | |||||||
chr13:21013963 | C | G | 1 | a0003c0003t0002g0188 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.343-22559G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013963 | |||||||
chr13:21013977 | CAAA | C | 13 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(10): Show |
13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-22576_343-2257 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013977 | |||||||
chr13:21014110 | A | G | 13 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(10): Show |
13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-22706T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014110 | |||||||
chr13:21014191 | G | A | 13 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(10): Show |
13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-22787C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014191 | |||||||
chr13:21014243 | C | A | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-22839G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014243 | |||||||
chr13:21014243 | C | G | 4 | a0001c0001t0001g0196 a0004c0004t0005g0197 a0004c0004t0005g0227 others(1): Show |
4 | HG01884.hp2 HG02735.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-22839G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014243 | |||||||
chr13:21014597 | C | T | 10 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-23193G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014597 | |||||||
chr13:21014769 | G | C | 2 | a0003c0007t0008g0048 a0003c0007t0008g0072 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.343-23365C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014769 | |||||||
chr13:21014981 | G | A | 73 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(70): Show |
74 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-23577C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014981 | |||||||
chr13:21015201 | G | A | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-23797C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21015201 | |||||||
chr13:21015586 | G | C | 2 | a0002c0034t0035g0029 a0004c0004t0028g0027 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.343-24182C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21015586 | |||||||
chr13:21015819 | C | T | 1 | a0002c0024t0023g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.343-24415G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21015819 | |||||||
chr13:21015866 | A | G | 2 | a0003c0003t0004g0298 a0003c0003t0004g0299 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.343-24462T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21015866 | |||||||
chr13:21015950 | C | T | 102 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(99): Show |
103 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.343-24546G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21015950 | |||||||
chr13:21016145 | A | G | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.343-24741T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016145 | |||||||
chr13:21016470 | G | A | 3 | a0002c0024t0023g0040 a0002c0034t0035g0029 a0004c0004t0028g0027 |
3 | HG00639.hp1 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.343-25066C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016470 | |||||||
chr13:21016493 | T | C | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-25089A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016493 | |||||||
chr13:21016525 | C | T | 5 | a0002c0002t0011g0036 a0005c0012t0001g0035 a0005c0012t0002g0030 others(2): Show |
5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-25121G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016525 | |||||||
chr13:21016599 | G | A | 6 | a0003c0008t0009g0292 a0003c0008t0009g0294 a0004c0004t0019g0028 others(3): Show |
6 | HG01433.hp2 HG02258.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-25195C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016599 | |||||||
chr13:21016793 | C | A | 1 | a0003c0003t0007g0105 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.343-25389G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016793 | |||||||
chr13:21016838 | T | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0209 |
2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.343-25434A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016838 | |||||||
chr13:21016849 | A | C | 78 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(75): Show |
79 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.343-25445T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016849 | |||||||
chr13:21017054 | C | T | 3 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0244 |
3 | NA18945.hp1 NA18973.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.343-25650G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017054 | |||||||
chr13:21017167 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.343-25763T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017167 | |||||||
chr13:21017314 | G | C | 1 | a0004c0035t0009g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.343-25910C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017314 | |||||||
chr13:21017457 | G | A | 123 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(120): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.343-26053C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017457 | |||||||
chr13:21017625 | CT | C | 290 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(287): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.343-26222delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017625 | |||||||
chr13:21017652 | A | C | 72 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(69): Show |
73 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.343-26248T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017652 | |||||||
chr13:21017868 | C | T | 1 | a0004c0004t0014g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.343-26464G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017868 | |||||||
chr13:21018389 | G | GC | 174 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(171): Show |
176 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.343-26986_343-2698 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018389 | |||||||
chr13:21018445 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.343-27041C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018445 | |||||||
chr13:21018555 | T | G | 299 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(296): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.342+27130A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018555 | |||||||
chr13:21018572 | C | T | 1 | a0003c0007t0016g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.342+27113G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018572 | |||||||
chr13:21018692 | C | T | 6 | a0003c0008t0009g0292 a0003c0008t0009g0294 a0004c0004t0019g0028 others(3): Show |
6 | HG01433.hp2 HG02258.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+26993G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018692 | |||||||
chr13:21018723 | G | A | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.342+26962C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018723 | |||||||
chr13:21018980 | C | G | 174 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(171): Show |
176 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.342+26705G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018980 | |||||||
chr13:21019155 | T | C | 6 | a0001c0001t0001g0231 a0001c0001t0010g0162 a0001c0001t0010g0163 others(3): Show |
6 | HG00423.hp2 NA18952.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+26530A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019155 | |||||||
chr13:21019292 | G | A | 72 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(69): Show |
73 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.342+26393C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019292 | |||||||
chr13:21019298 | G | GTTA | 3 | a0002c0006t0004g0018 a0002c0006t0004g0169 a0004c0004t0014g0297 |
3 | HG01943.hp2 HG02647.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.342+26384_342+2638 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | |||||||
chr13:21019298 | GTTA | G | 121 | a0001c0001t0001g0090 a0001c0001t0001g0176 a0001c0001t0001g0181 others(118): Show |
123 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.342+26384_342+2638 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | |||||||
chr13:21019298 | GTTATTA | G | 84 | a0001c0001t0001g0092 a0001c0001t0001g0180 a0001c0001t0001g0192 others(81): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.342+26381_342+2638 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | |||||||
chr13:21019298 | GTTATTAT others(2): Show |
G | 52 | a0001c0001t0001g0207 a0001c0001t0001g0231 a0001c0001t0001g0243 others(49): Show |
52 | HG00423.hp2 HG00642.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.342+26378_342+2638 others(13): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | |||||||
chr13:21019298 | GTTATTAT others(5): Show |
G | 9 | a0001c0001t0006g0191 a0002c0006t0004g0025 a0003c0003t0002g0011 others(6): Show |
9 | HG01496.hp2 HG03490.hp2 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.342+26375_342+2638 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | |||||||
chr13:21019298 | GTTATTAT others(8): Show |
G | 12 | a0001c0001t0001g0212 a0003c0003t0004g0257 a0003c0003t0025g0285 others(9): Show |
12 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.342+26372_342+2638 others(19): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | |||||||
chr13:21019298 | GTTATTAT others(14): Show |
G | 2 | a0008c0018t0010g0067 a0008c0018t0010g0068 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.342+26366_342+2638 others(25): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | |||||||
chr13:21019301 | A | G | 2 | a0004c0004t0001g0300 a0004c0004t0001g0301 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.342+26384T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019301 | |||||||
chr13:21019313 | A | C | 1 | a0004c0015t0018g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.342+26372T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019313 | |||||||
chr13:21019322 | A | C | 82 | a0002c0002t0003g0094 a0002c0002t0003g0095 a0002c0002t0003g0096 others(79): Show |
82 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.342+26363T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019322 | |||||||
chr13:21019328 | A | C | 5 | a0002c0024t0023g0040 a0002c0034t0035g0029 a0003c0008t0009g0088 others(2): Show |
5 | HG00639.hp1 HG01243.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+26357T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019328 | |||||||
chr13:21019328 | A | G | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.342+26357T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019328 | |||||||
chr13:21019388 | G | A | 6 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+26297C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019388 | |||||||
chr13:21019493 | A | ATTT | 98 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(95): Show |
99 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.342+26189_342+2619 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019493 | |||||||
chr13:21019493 | A | ATTTT | 18 | a0001c0022t0004g0010 a0002c0002t0003g0155 a0002c0002t0010g0279 others(15): Show |
18 | HG01243.hp2 HG02055.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+26188_342+2619 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019493 | |||||||
chr13:21019493 | A | ATTTTT | 12 | a0003c0005t0002g0066 a0003c0007t0008g0046 a0003c0007t0008g0047 others(9): Show |
12 | HG01109.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.342+26187_342+2619 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019493 | |||||||
chr13:21019493 | A | ATTTTTT | 38 | a0001c0010t0001g0054 a0001c0010t0015g0006 a0002c0017t0006g0007 others(35): Show |
38 | HG00621.hp2 HG00741.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.342+26186_342+2619 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019493 | |||||||
chr13:21019493 | A | ATTTTTTT | 7 | a0001c0010t0001g0064 a0003c0003t0002g0021 a0003c0005t0002g0055 others(4): Show |
7 | HG00642.hp2 HG01175.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+26185_342+2619 others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019493 | |||||||
chr13:21019531 | C | G | 1 | a0001c0001t0001g0230 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.342+26154G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019531 | |||||||
chr13:21019632 | C | T | 1 | a0002c0002t0003g0102 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.342+26053G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019632 | |||||||
chr13:21019668 | CA | C | 189 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(186): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.342+26016delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019668 | |||||||
chr13:21019668 | CAA | C | 73 | a0001c0001t0001g0195 a0001c0001t0001g0244 a0001c0001t0010g0162 others(70): Show |
73 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.342+26015_342+2601 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019668 | |||||||
chr13:21019744 | C | T | 1 | a0002c0002t0003g0101 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.342+25941G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019744 | |||||||
chr13:21019840 | G | C | 67 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(64): Show |
67 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.342+25845C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019840 | |||||||
chr13:21019887 | T | C | 2 | a0003c0008t0009g0088 a0009c0033t0001g0302 |
2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.342+25798A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019887 | |||||||
chr13:21019912 | C | T | 174 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(171): Show |
176 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.342+25773G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019912 | |||||||
chr13:21019973 | T | TA | 11 | a0002c0002t0003g0111 a0002c0002t0003g0155 a0002c0024t0023g0040 others(8): Show |
11 | HG00639.hp1 HG01175.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.342+25711dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019973 | |||||||
chr13:21019973 | T | TAA | 11 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(8): Show |
11 | HG00597.hp2 HG01496.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+25710_342+2571 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019973 | |||||||
chr13:21020085 | G | T | 1 | a0002c0002t0003g0142 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.342+25600C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020085 | |||||||
chr13:21020146 | T | TAAAATAT others(1): Show |
99 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(96): Show |
100 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.342+25531_342+2553 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020146 | |||||||
chr13:21020151 | T | C | 2 | a0003c0008t0009g0088 a0009c0033t0001g0302 |
2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.342+25534A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020151 | |||||||
chr13:21020321 | T | C | 2 | a0003c0003t0004g0298 a0003c0003t0004g0299 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.342+25364A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020321 | |||||||
chr13:21020524 | GA | G | 174 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(171): Show |
176 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.342+25160delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020524 | |||||||
chr13:21020560 | C | T | 123 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(120): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.342+25125G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020560 | |||||||
chr13:21020796 | C | T | 123 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(120): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.342+24889G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020796 | |||||||
chr13:21020894 | C | T | 1 | a0001c0001t0002g0166 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.342+24791G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020894 | |||||||
chr13:21021070 | T | C | 1 | a0004c0004t0001g0300 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.342+24615A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021070 | |||||||
chr13:21021259 | G | A | 73 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(70): Show |
74 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.342+24426C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021259 | |||||||
chr13:21021319 | G | A | 57 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(54): Show |
57 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.342+24366C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021319 | |||||||
chr13:21021332 | G | A | 3 | a0001c0001t0001g0231 a0001c0001t0010g0162 a0001c0001t0010g0163 |
3 | HG00423.hp2 NA18971.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.342+24353C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021332 | |||||||
chr13:21021450 | G | A | 4 | a0002c0002t0003g0126 a0002c0002t0003g0128 a0002c0002t0003g0129 others(1): Show |
4 | NA18959.hp2 NA19004.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+24235C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021450 | |||||||
chr13:21021474 | C | CA | 88 | a0001c0001t0001g0092 a0001c0001t0001g0176 a0001c0001t0001g0180 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.342+24210dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | |||||||
chr13:21021474 | C | CAA | 57 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0001g0193 others(54): Show |
57 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.342+24209_342+2421 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | |||||||
chr13:21021474 | C | CAAA | 12 | a0001c0001t0001g0220 a0003c0003t0002g0172 a0003c0003t0004g0298 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.342+24208_342+2421 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | |||||||
chr13:21021474 | C | CAAAAAAA others(3): Show |
1 | a0003c0008t0009g0294 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.342+24201_342+2421 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | |||||||
chr13:21021474 | CAAAAAAA others(3): Show |
C | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.342+24201_342+2421 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | |||||||
chr13:21021474 | CAAAAAAA others(4): Show |
C | 2 | a0002c0002t0003g0122 a0002c0002t0003g0133 |
2 | NA19002.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.342+24200_342+2421 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | |||||||
chr13:21021474 | CAAAAAAA others(5): Show |
C | 100 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(97): Show |
101 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.342+24199_342+2421 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | |||||||
chr13:21021476 | A | C | 1 | a0001c0001t0001g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.342+24209T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021476 | |||||||
chr13:21021534 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.342+24151C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021534 | |||||||
chr13:21021680 | C | T | 1 | a0002c0002t0003g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.342+24005G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021680 | |||||||
chr13:21021739 | C | A | 73 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(70): Show |
74 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.342+23946G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021739 | |||||||
chr13:21021952 | T | A | 1 | a0001c0001t0001g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.342+23733A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021952 | |||||||
chr13:21021953 | A | T | 1 | a0001c0001t0001g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.342+23732T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021953 | |||||||
chr13:21022044 | G | A | 145 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(142): Show |
147 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(144): Show |
intron_variant | MODIFIER | c.342+23641C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022044 | |||||||
chr13:21022067 | C | T | 1 | a0002c0024t0023g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.342+23618G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022067 | |||||||
chr13:21022111 | C | A | 1 | a0002c0002t0003g0122 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.342+23574G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022111 | |||||||
chr13:21022236 | CTA | C | 18 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(15): Show |
18 | HG00597.hp2 HG00639.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+23447_342+2344 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022236 | |||||||
chr13:21022263 | C | T | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+23422G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022263 | |||||||
chr13:21022345 | G | C | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.342+23340C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022345 | |||||||
chr13:21022381 | C | T | 174 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(171): Show |
176 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.342+23304G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022381 | |||||||
chr13:21022422 | G | T | 4 | a0004c0004t0005g0263 a0004c0004t0005g0267 a0004c0004t0005g0268 others(1): Show |
4 | HG01106.hp1 HG01433.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+23263C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022422 | |||||||
chr13:21022424 | C | T | 1 | a0003c0009t0032g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.342+23261G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022424 | |||||||
chr13:21022440 | CCCTGACA others(41): Show |
C | 1 | a0001c0001t0001g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.342+23197_342+2324 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022440 | |||||||
chr13:21022449 | C | T | 3 | a0004c0015t0018g0044 a0004c0019t0020g0303 a0004c0019t0020g0304 |
3 | HG01243.hp1 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.342+23236G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022449 | |||||||
chr13:21022814 | TA | T | 18 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(15): Show |
18 | HG00597.hp2 HG00639.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+22870delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022814 | |||||||
chr13:21022913 | T | C | 10 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.342+22772A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022913 | |||||||
chr13:21023146 | AGGGCTCC | A | 72 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(69): Show |
73 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.342+22532_342+2253 others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023146 | |||||||
chr13:21023157 | C | T | 72 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(69): Show |
73 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.342+22528G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023157 | |||||||
chr13:21023275 | C | A | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+22410G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023275 | |||||||
chr13:21023323 | C | G | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.342+22362G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023323 | |||||||
chr13:21023495 | C | CCTCTGTT others(20): Show |
1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.342+22163_342+2218 others(31): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023495 | |||||||
chr13:21023501 | T | C | 1 | a0001c0011t0001g0081 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.342+22184A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023501 | |||||||
chr13:21023649 | A | C | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+22036T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023649 | |||||||
chr13:21023658 | A | C | 1 | a0001c0001t0013g0187 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.342+22027T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023658 | |||||||
chr13:21023665 | AAAAAAAA others(12): Show |
A | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.342+22001_342+2201 others(23): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023665 | |||||||
chr13:21023666 | AAAAAAAA others(11): Show |
A | 5 | a0001c0001t0001g0193 a0001c0001t0001g0207 a0001c0001t0001g0262 others(2): Show |
5 | HG01070.hp1 HG01167.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+22001_342+2201 others(22): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023666 | |||||||
chr13:21023667 | AAAAAAAA others(10): Show |
A | 109 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.342+22001_342+2201 others(21): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023667 | |||||||
chr13:21023668 | AAAAAAAA others(9): Show |
A | 9 | a0001c0001t0001g0222 a0001c0001t0001g0237 a0001c0001t0002g0002 others(6): Show |
10 | HG00597.hp1 HG02074.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.342+22001_342+2201 others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023668 | |||||||
chr13:21023670 | AAAAAAAA others(7): Show |
A | 5 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(2): Show |
5 | HG02451.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+22001_342+2201 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023670 | |||||||
chr13:21023671 | AAAAAAAA others(6): Show |
A | 2 | a0004c0019t0020g0303 a0005c0012t0002g0030 |
2 | HG01243.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.342+22001_342+2201 others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023671 | |||||||
chr13:21023672 | AAAAAAAA others(5): Show |
A | 4 | a0002c0002t0011g0036 a0005c0012t0001g0035 a0005c0012t0002g0032 others(1): Show |
4 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+22001_342+2201 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023672 | |||||||
chr13:21023673 | AAAAAAAA others(4): Show |
A | 1 | a0004c0004t0028g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.342+22001_342+2201 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023673 | |||||||
chr13:21023674 | AAAAAAAA others(3): Show |
A | 11 | a0001c0011t0001g0001 a0001c0011t0001g0082 a0001c0011t0001g0086 others(8): Show |
12 | HG01243.hp2 HG02155.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.342+22001_342+2201 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023674 | |||||||
chr13:21023675 | AAAAAAAA others(2): Show |
A | 42 | a0001c0011t0001g0081 a0002c0002t0003g0094 a0002c0002t0003g0095 others(39): Show |
42 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.342+22001_342+2200 others(13): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023675 | |||||||
chr13:21023676 | AAAAAAAA others(1): Show |
A | 44 | a0002c0002t0003g0098 a0002c0002t0003g0107 a0002c0002t0003g0108 others(41): Show |
45 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.342+22001_342+2200 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023676 | |||||||
chr13:21023677 | AAAAAAAC | A | 29 | a0001c0010t0001g0054 a0002c0006t0004g0024 a0002c0006t0004g0210 others(26): Show |
29 | HG01167.hp2 HG01168.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.342+22001_342+2200 others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023677 | |||||||
chr13:21023678 | AAAAAAC | A | 20 | a0001c0010t0001g0064 a0001c0010t0015g0006 a0003c0003t0002g0019 others(17): Show |
20 | HG00642.hp2 HG00741.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.342+22001_342+2200 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023678 | |||||||
chr13:21023679 | AAAAAC | A | 11 | a0002c0017t0006g0007 a0003c0003t0025g0285 a0003c0005t0002g0062 others(8): Show |
11 | HG00621.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+22001_342+2200 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023679 | |||||||
chr13:21023684 | C | A | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.342+22001G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023684 | |||||||
chr13:21023723 | C | T | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+21962G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023723 | |||||||
chr13:21023745 | G | T | 78 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(75): Show |
79 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.342+21940C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023745 | |||||||
chr13:21023761 | G | T | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.342+21924C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023761 | |||||||
chr13:21023763 | C | T | 4 | a0002c0002t0010g0279 a0002c0028t0041g0280 a0005c0016t0014g0037 others(1): Show |
4 | HG02965.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+21922G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023763 | |||||||
chr13:21023768 | A | G | 174 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(171): Show |
176 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.342+21917T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023768 | |||||||
chr13:21023836 | G | A | 6 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+21849C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023836 | |||||||
chr13:21023842 | G | T | 1 | a0002c0002t0003g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.342+21843C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023842 | |||||||
chr13:21023881 | G | C | 1 | a0002c0002t0003g0101 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.342+21804C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023881 | |||||||
chr13:21023917 | GA | G | 3 | a0001c0001t0001g0231 a0001c0001t0010g0162 a0001c0001t0010g0163 |
3 | HG00423.hp2 NA18971.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.342+21767delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023917 | |||||||
chr13:21023934 | T | C | 57 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(54): Show |
57 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.342+21751A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023934 | |||||||
chr13:21023968 | C | A | 18 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(15): Show |
18 | HG00597.hp2 HG00639.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+21717G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023968 | |||||||
chr13:21024089 | T | C | 2 | a0003c0003t0004g0298 a0003c0003t0004g0299 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.342+21596A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024089 | |||||||
chr13:21024093 | C | CA | 9 | a0001c0001t0001g0090 a0001c0001t0001g0209 a0001c0001t0002g0226 others(6): Show |
9 | HG00741.hp1 HG01109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.342+21591dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024093 | |||||||
chr13:21024093 | CA | C | 93 | a0001c0010t0001g0064 a0001c0011t0001g0001 a0001c0011t0001g0081 others(90): Show |
94 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+21591delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024093 | |||||||
chr13:21024093 | CAA | C | 69 | a0001c0010t0001g0054 a0001c0010t0015g0006 a0001c0022t0004g0010 others(66): Show |
70 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.342+21590_342+2159 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024093 | |||||||
chr13:21024093 | CAAAA | C | 6 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+21588_342+2159 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024093 | |||||||
chr13:21024110 | A | G | 75 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(72): Show |
76 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.342+21575T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024110 | |||||||
chr13:21024111 | A | G | 1 | a0003c0003t0002g0019 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.342+21574T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024111 | |||||||
chr13:21024119 | A | G | 5 | a0002c0002t0011g0036 a0005c0012t0001g0035 a0005c0012t0002g0030 others(2): Show |
5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+21566T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024119 | |||||||
chr13:21024330 | G | C | 1 | a0002c0006t0004g0022 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.342+21355C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024330 | |||||||
chr13:21024389 | T | G | 1 | a0001c0001t0010g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.342+21296A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024389 | |||||||
chr13:21024553 | C | T | 1 | a0003c0003t0002g0253 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.342+21132G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024553 | |||||||
chr13:21024579 | CCTCACGG others(7): Show |
C | 3 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 |
3 | HG02451.hp2 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.342+21092_342+2110 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024579 | |||||||
chr13:21024583 | A | T | 1 | a0002c0006t0004g0254 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.342+21102T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024583 | |||||||
chr13:21024585 | G | A | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+21100C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024585 | |||||||
chr13:21024604 | C | T | 4 | a0002c0002t0010g0279 a0002c0028t0041g0280 a0005c0016t0014g0037 others(1): Show |
4 | HG02965.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+21081G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024604 | |||||||
chr13:21024682 | C | T | 2 | a0004c0004t0001g0300 a0004c0004t0001g0301 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.342+21003G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024682 | |||||||
chr13:21024689 | TA | T | 246 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(243): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.342+20995delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024689 | |||||||
chr13:21024689 | TAA | T | 8 | a0001c0001t0004g0274 a0001c0001t0017g0130 a0002c0028t0041g0280 others(5): Show |
8 | HG01243.hp2 HG01516.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.342+20994_342+2099 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024689 | |||||||
chr13:21024740 | T | A | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+20945A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024740 | |||||||
chr13:21024807 | T | C | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.342+20878A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024807 | |||||||
chr13:21025217 | TA | T | 233 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(230): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.342+20467delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025217 | |||||||
chr13:21025235 | T | A | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+20450A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025235 | |||||||
chr13:21025249 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0221 a0001c0001t0010g0112 |
3 | NA18998.hp1 NA19005.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.342+20436C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025249 | |||||||
chr13:21025338 | G | A | 1 | a0006c0013t0007g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.342+20347C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025338 | |||||||
chr13:21025393 | C | CA | 22 | a0001c0001t0001g0090 a0001c0001t0001g0201 a0001c0001t0001g0231 others(19): Show |
22 | HG00423.hp2 HG00741.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.342+20291dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025393 | |||||||
chr13:21025406 | A | C | 72 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(69): Show |
73 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.342+20279T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025406 | |||||||
chr13:21025413 | A | AAC | 24 | a0001c0010t0001g0064 a0001c0010t0015g0006 a0002c0017t0006g0007 others(21): Show |
24 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.342+20271_342+2027 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025413 | |||||||
chr13:21025413 | A | AC | 54 | a0002c0002t0010g0279 a0002c0006t0004g0023 a0002c0014t0018g0041 others(51): Show |
55 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.342+20271_342+2027 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025413 | |||||||
chr13:21025413 | A | C | 94 | a0001c0010t0001g0054 a0001c0011t0001g0001 a0001c0011t0001g0081 others(91): Show |
95 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.342+20272T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025413 | |||||||
chr13:21025685 | G | A | 67 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(64): Show |
67 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.342+20000C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025685 | |||||||
chr13:21025763 | C | T | 72 | a0001c0010t0001g0054 a0001c0010t0001g0064 a0001c0010t0015g0006 others(69): Show |
73 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.342+19922G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025763 | |||||||
chr13:21026167 | G | A | 2 | a0002c0002t0011g0036 a0005c0012t0001g0035 |
2 | HG00735.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.342+19518C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026167 | |||||||
chr13:21026188 | A | G | 1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.342+19497T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026188 | |||||||
chr13:21026326 | TA | T | 244 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(241): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.342+19358delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026326 | |||||||
chr13:21026338 | A | C | 1 | a0004c0015t0005g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.342+19347T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026338 | |||||||
chr13:21026654 | T | A | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.342+19031A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026654 | |||||||
chr13:21026731 | G | A | 1 | a0002c0027t0039g0114 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.342+18954C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026731 | |||||||
chr13:21026734 | T | C | 1 | a0001c0011t0001g0082 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.342+18951A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026734 | |||||||
chr13:21026773 | T | C | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+18912A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026773 | |||||||
chr13:21026965 | CTGA | C | 6 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+18717_342+1871 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026965 | |||||||
chr13:21026967 | G | A | 5 | a0002c0024t0023g0040 a0002c0034t0035g0029 a0003c0008t0009g0088 others(2): Show |
5 | HG00639.hp1 HG01243.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+18718C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026967 | |||||||
chr13:21027075 | T | C | 102 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(99): Show |
103 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.342+18610A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21027075 | |||||||
chr13:21027544 | G | A | 2 | a0003c0003t0002g0170 a0003c0003t0002g0229 |
2 | HG01070.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.342+18141C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21027544 | |||||||
chr13:21027570 | T | C | 10 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.342+18115A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21027570 | |||||||
chr13:21027642 | A | G | 1 | a0002c0002t0003g0107 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.342+18043T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21027642 | |||||||
chr13:21027649 | G | A | 255 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(252): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.342+18036C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21027649 | |||||||
chr13:21027748 | C | T | 1 | a0003c0003t0001g0234 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.342+17937G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21027748 | |||||||
chr13:21028036 | C | T | 1 | a0003c0009t0031g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.342+17649G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028036 | |||||||
chr13:21028176 | G | A | 2 | a0002c0002t0003g0124 a0002c0024t0023g0040 |
2 | HG00639.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.342+17509C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028176 | |||||||
chr13:21028199 | G | A | 2 | a0001c0001t0006g0232 a0001c0031t0006g0185 |
2 | HG00423.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.342+17486C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028199 | |||||||
chr13:21028391 | T | C | 4 | a0003c0003t0004g0298 a0003c0003t0004g0299 a0004c0004t0004g0296 others(1): Show |
4 | HG02647.hp2 HG03486.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+17294A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028391 | |||||||
chr13:21028493 | A | C | 5 | a0002c0002t0011g0036 a0005c0012t0001g0035 a0005c0012t0002g0030 others(2): Show |
5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+17192T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028493 | |||||||
chr13:21028512 | ATATTTTG others(17): Show |
A | 1 | a0002c0002t0003g0122 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.342+17149_342+1717 others(28): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028512 | |||||||
chr13:21028615 | G | C | 78 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(75): Show |
79 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.342+17070C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028615 | |||||||
chr13:21028663 | C | T | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.342+17022G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028663 | |||||||
chr13:21028682 | T | C | 6 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+17003A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028682 | |||||||
chr13:21028684 | C | T | 13 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(10): Show |
13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.342+17001G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028684 | |||||||
chr13:21028858 | G | A | 1 | a0002c0002t0003g0147 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.342+16827C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028858 | |||||||
chr13:21028897 | G | A | 6 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+16788C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028897 | |||||||
chr13:21029003 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.342+16682A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029003 | |||||||
chr13:21029073 | T | C | 1 | a0004c0004t0005g0268 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.342+16612A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029073 | |||||||
chr13:21029094 | C | T | 1 | a0003c0005t0002g0052 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.342+16591G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029094 | |||||||
chr13:21029197 | T | C | 13 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(10): Show |
13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.342+16488A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029197 | |||||||
chr13:21029284 | G | A | 104 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(101): Show |
105 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.342+16401C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029284 | |||||||
chr13:21029364 | A | C | 14 | a0003c0003t0004g0298 a0003c0003t0004g0299 a0003c0007t0036g0053 others(11): Show |
14 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.342+16321T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029364 | |||||||
chr13:21029501 | G | C | 2 | a0002c0002t0011g0036 a0005c0012t0001g0035 |
2 | HG00735.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.342+16184C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029501 | |||||||
chr13:21029503 | T | C | 13 | a0003c0003t0004g0298 a0003c0003t0004g0299 a0003c0007t0036g0053 others(10): Show |
13 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.342+16182A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029503 | |||||||
chr13:21029541 | C | T | 4 | a0002c0002t0010g0279 a0002c0028t0041g0280 a0005c0016t0014g0037 others(1): Show |
4 | HG02965.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+16144G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029541 | |||||||
chr13:21029567 | C | T | 1 | a0002c0006t0004g0025 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.342+16118G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029567 | |||||||
chr13:21029575 | G | A | 1 | a0002c0002t0011g0282 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.342+16110C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029575 | |||||||
chr13:21029715 | C | T | 1 | a0002c0002t0006g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.342+15970G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029715 | |||||||
chr13:21029716 | G | A | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+15969C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029716 | |||||||
chr13:21029956 | T | C | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.342+15729A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029956 | |||||||
chr13:21030038 | T | C | 254 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(251): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.342+15647A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030038 | |||||||
chr13:21030039 | G | A | 6 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+15646C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030039 | |||||||
chr13:21030134 | G | A | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+15551C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030134 | |||||||
chr13:21030136 | A | G | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+15549T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030136 | |||||||
chr13:21030149 | A | C | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+15536T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030149 | |||||||
chr13:21030317 | T | C | 255 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(252): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.342+15368A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030317 | |||||||
chr13:21030371 | C | T | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+15314G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030371 | |||||||
chr13:21030457 | C | T | 6 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+15228G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030457 | |||||||
chr13:21030506 | G | A | 2 | a0002c0034t0035g0029 a0004c0004t0028g0027 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.342+15179C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030506 | |||||||
chr13:21030583 | C | CCGGA | 5 | a0001c0001t0001g0220 a0003c0003t0002g0177 a0003c0003t0002g0178 others(2): Show |
5 | NA18952.hp2 NA18982.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+15101_342+1510 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030583 | |||||||
chr13:21030588 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.342+15097A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030588 | |||||||
chr13:21030591 | C | CA | 6 | a0001c0010t0001g0064 a0003c0003t0002g0188 a0003c0005t0002g0063 others(3): Show |
6 | HG00621.hp2 HG02135.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+15093dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030591 | |||||||
chr13:21030593 | AAAAAAAA others(12): Show |
A | 13 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(10): Show |
13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.342+15073_342+1509 others(23): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030593 | |||||||
chr13:21030607 | A | G | 1 | a0001c0001t0013g0205 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.342+15078T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030607 | |||||||
chr13:21030608 | A | AG | 109 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(106): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.342+15076_342+1507 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030608 | |||||||
chr13:21030608 | A | G | 84 | a0001c0001t0001g0240 a0001c0001t0002g0203 a0001c0001t0003g0161 others(81): Show |
84 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.342+15077T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030608 | |||||||
chr13:21030609 | A | G | 4 | a0001c0001t0001g0220 a0003c0003t0002g0177 a0003c0003t0002g0178 others(1): Show |
4 | NA18952.hp2 NA18982.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+15076T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030609 | |||||||
chr13:21030612 | G | A | 214 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.342+15073C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030612 | |||||||
chr13:21030612 | GA | G | 19 | a0001c0001t0013g0205 a0001c0022t0004g0010 a0002c0014t0018g0041 others(16): Show |
19 | HG01243.hp1 HG01433.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.342+15072delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030612 | |||||||
chr13:21030613 | A | AG | 12 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 others(9): Show |
12 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.342+15071_342+1507 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030613 | |||||||
chr13:21030613 | A | G | 201 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.342+15072T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030613 | |||||||
chr13:21030614 | A | G | 4 | a0001c0001t0001g0220 a0003c0003t0002g0177 a0003c0003t0002g0178 others(1): Show |
4 | NA18952.hp2 NA18982.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+15071T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030614 | |||||||
chr13:21030617 | A | G | 2 | a0003c0008t0009g0088 a0009c0033t0001g0302 |
2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.342+15068T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030617 | |||||||
chr13:21030866 | T | C | 1 | a0001c0001t0006g0190 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.342+14819A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030866 | |||||||
chr13:21030869 | A | C | 244 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(241): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.342+14816T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030869 | |||||||
chr13:21030914 | A | C | 3 | a0001c0001t0001g0193 a0003c0005t0002g0069 a0003c0005t0002g0070 |
3 | HG01167.hp2 HG01168.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.342+14771T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030914 | |||||||
chr13:21031046 | T | G | 1 | a0003c0009t0008g0307 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.342+14639A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031046 | |||||||
chr13:21031072 | T | G | 1 | a0004c0004t0005g0249 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.342+14613A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031072 | |||||||
chr13:21031290 | T | C | 2 | a0002c0034t0035g0029 a0004c0004t0028g0027 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.342+14395A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031290 | |||||||
chr13:21031347 | T | C | 3 | a0001c0001t0006g0168 a0001c0001t0006g0182 a0001c0001t0006g0191 |
3 | NA18994.hp2 NA19057.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.342+14338A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031347 | |||||||
chr13:21031349 | A | G | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.342+14336T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031349 | |||||||
chr13:21031421 | A | G | 89 | a0001c0001t0003g0161 a0001c0001t0010g0112 a0001c0001t0047g0100 others(86): Show |
90 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.342+14264T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031421 | |||||||
chr13:21031616 | T | C | 1 | a0001c0001t0034g0214 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.342+14069A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031616 | |||||||
chr13:21032022 | G | A | 14 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(11): Show |
14 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.342+13663C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032022 | |||||||
chr13:21032163 | T | A | 1 | a0002c0002t0003g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.342+13522A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032163 | |||||||
chr13:21032288 | CAG | C | 151 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(148): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.342+13395_342+1339 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032288 | |||||||
chr13:21032328 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.342+13357G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032328 | |||||||
chr13:21032545 | G | C | 151 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(148): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.342+13140C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032545 | |||||||
chr13:21032669 | T | C | 2 | a0002c0002t0003g0157 a0002c0002t0003g0158 |
2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.342+13016A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032669 | |||||||
chr13:21032731 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.342+12954G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032731 | |||||||
chr13:21032773 | C | G | 7 | a0003c0008t0009g0088 a0003c0009t0008g0307 a0003c0009t0009g0306 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+12912G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032773 | |||||||
chr13:21032801 | A | G | 1 | a0002c0002t0010g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.342+12884T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032801 | |||||||
chr13:21032919 | G | T | 122 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(119): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.342+12766C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032919 | |||||||
chr13:21032950 | C | G | 1 | a0003c0005t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.342+12735G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032950 | |||||||
chr13:21033055 | G | A | 1 | a0009c0033t0001g0302 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.342+12630C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033055 | |||||||
chr13:21033293 | G | C | 14 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(11): Show |
14 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.342+12392C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033293 | |||||||
chr13:21033301 | G | A | 7 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(4): Show |
7 | HG00639.hp1 HG01243.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.342+12384C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033301 | |||||||
chr13:21033461 | A | G | 151 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(148): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.342+12224T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033461 | |||||||
chr13:21033595 | C | T | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.342+12090G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033595 | |||||||
chr13:21033621 | G | A | 134 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(131): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.342+12064C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033621 | |||||||
chr13:21033631 | T | C | 7 | a0003c0008t0009g0088 a0003c0009t0008g0307 a0003c0009t0009g0306 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+12054A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033631 | |||||||
chr13:21034004 | T | C | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+11681A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034004 | |||||||
chr13:21034251 | C | CACAGCCA others(5): Show |
1 | a0005c0016t0005g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.342+11422_342+1143 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034251 | |||||||
chr13:21034338 | T | C | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.342+11347A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034338 | |||||||
chr13:21034533 | C | T | 1 | a0003c0003t0025g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.342+11152G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034533 | |||||||
chr13:21034565 | G | C | 3 | a0003c0003t0002g0172 a0003c0003t0002g0173 a0003c0003t0002g0175 |
3 | HG01074.hp2 HG01099.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.342+11120C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034565 | |||||||
chr13:21034582 | T | C | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+11103A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034582 | |||||||
chr13:21034611 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.342+11074G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034611 | |||||||
chr13:21034700 | C | G | 126 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.342+10985G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034700 | |||||||
chr13:21034715 | CACCTGGG others(87): Show |
C | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+10876_342+1096 others(98): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034715 | |||||||
chr13:21034732 | G | C | 3 | a0004c0004t0005g0197 a0004c0004t0005g0227 a0004c0004t0005g0228 |
3 | HG02735.hp2 HG03490.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.342+10953C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034732 | |||||||
chr13:21034832 | A | G | 123 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(120): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.342+10853T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034832 | |||||||
chr13:21034912 | C | T | 3 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 |
3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+10773G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034912 | |||||||
chr13:21035001 | C | T | 3 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 |
3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+10684G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035001 | |||||||
chr13:21035010 | C | A | 127 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(124): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.342+10675G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035010 | |||||||
chr13:21035046 | CAT | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0037g0186 |
3 | HG00280.hp1 HG01361.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.342+10637_342+1063 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035046 | |||||||
chr13:21035143 | T | A | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+10542A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035143 | |||||||
chr13:21035213 | G | A | 9 | a0002c0002t0011g0036 a0003c0009t0026g0031 a0003c0009t0031g0033 others(6): Show |
9 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.342+10472C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035213 | |||||||
chr13:21035447 | C | T | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+10238G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035447 | |||||||
chr13:21035577 | G | A | 123 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(120): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.342+10108C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035577 | |||||||
chr13:21035625 | G | A | 2 | a0001c0001t0002g0216 a0003c0008t0008g0289 |
2 | HG01081.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.342+10060C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035625 | |||||||
chr13:21035698 | T | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0037g0186 |
3 | HG00280.hp1 HG01361.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.342+9987A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035698 | |||||||
chr13:21035727 | T | G | 2 | a0003c0003t0002g0019 a0003c0003t0002g0021 |
2 | HG00642.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.342+9958A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035727 | |||||||
chr13:21035777 | G | A | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.342+9908C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035777 | |||||||
chr13:21035929 | T | G | 2 | a0004c0004t0001g0300 a0004c0004t0001g0301 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.342+9756A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035929 | |||||||
chr13:21036043 | C | T | 24 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(21): Show |
24 | HG00597.hp2 HG00642.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.342+9642G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036043 | |||||||
chr13:21036050 | C | T | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+9635G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036050 | |||||||
chr13:21036085 | C | T | 2 | a0002c0002t0003g0116 a0002c0002t0003g0134 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.342+9600G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036085 | |||||||
chr13:21036116 | G | A | 1 | a0004c0015t0005g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.342+9569C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036116 | |||||||
chr13:21036156 | G | A | 6 | a0003c0008t0009g0088 a0003c0009t0008g0307 a0003c0009t0009g0306 others(3): Show |
6 | HG01243.hp2 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+9529C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036156 | |||||||
chr13:21036176 | G | A | 1 | a0002c0002t0003g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.342+9509C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036176 | |||||||
chr13:21036209 | T | G | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+9476A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036209 | |||||||
chr13:21036330 | C | A | 3 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 |
3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+9355G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036330 | |||||||
chr13:21036419 | T | A | 1 | a0003c0007t0036g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+9266A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036419 | |||||||
chr13:21036512 | C | T | 24 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(21): Show |
24 | HG00597.hp2 HG00642.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.342+9173G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036512 | |||||||
chr13:21036644 | G | A | 2 | a0002c0034t0035g0029 a0004c0004t0028g0027 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.342+9041C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036644 | |||||||
chr13:21036667 | A | G | 161 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(158): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.342+9018T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036667 | |||||||
chr13:21036705 | G | A | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+8980C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036705 | |||||||
chr13:21036713 | C | T | 1 | a0003c0005t0033g0077 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.342+8972G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036713 | |||||||
chr13:21036767 | C | T | 1 | a0004c0015t0018g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.342+8918G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036767 | |||||||
chr13:21036774 | AAAC | A | 137 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.342+8908_342+8910d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036774 | |||||||
chr13:21037049 | G | C | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+8636C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037049 | |||||||
chr13:21037050 | C | G | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+8635G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037050 | |||||||
chr13:21037163 | G | A | 3 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 |
3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+8522C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037163 | |||||||
chr13:21037222 | T | C | 68 | a0001c0001t0003g0161 a0001c0001t0010g0112 a0001c0001t0047g0100 others(65): Show |
68 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.342+8463A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037222 | |||||||
chr13:21037268 | A | G | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+8417T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037268 | |||||||
chr13:21037334 | G | C | 1 | a0001c0001t0001g0220 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.342+8351C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037334 | |||||||
chr13:21037345 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.342+8340T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037345 | |||||||
chr13:21037469 | CG | C | 95 | a0001c0001t0003g0161 a0001c0001t0010g0112 a0001c0001t0047g0100 others(92): Show |
96 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.342+8215delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037469 | |||||||
chr13:21037470 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.342+8215C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037470 | |||||||
chr13:21037520 | A | G | 3 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 |
3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+8165T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037520 | |||||||
chr13:21037652 | C | T | 269 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(266): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.342+8033G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037652 | |||||||
chr13:21037743 | G | A | 1 | a0002c0002t0003g0113 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.342+7942C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037743 | |||||||
chr13:21037803 | GCCAGGGT others(8): Show |
G | 7 | a0003c0008t0009g0088 a0003c0009t0008g0307 a0003c0009t0009g0306 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+7867_342+7881d others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037803 | |||||||
chr13:21037810 | T | A | 1 | a0003c0007t0008g0072 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.342+7875A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037810 | |||||||
chr13:21037826 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.342+7859C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037826 | |||||||
chr13:21037840 | T | C | 12 | a0003c0003t0004g0298 a0003c0003t0004g0299 a0003c0008t0009g0292 others(9): Show |
12 | HG01433.hp2 HG02258.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.342+7845A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037840 | |||||||
chr13:21037879 | G | A | 1 | a0009c0033t0001g0302 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.342+7806C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037879 | |||||||
chr13:21037880 | T | C | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+7805A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037880 | |||||||
chr13:21037911 | AG | A | 4 | a0003c0005t0002g0050 a0003c0005t0002g0051 a0003c0005t0002g0073 others(1): Show |
4 | HG02257.hp1 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+7773delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037911 | |||||||
chr13:21037979 | C | T | 1 | a0003c0008t0008g0289 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.342+7706G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037979 | |||||||
chr13:21037989 | C | T | 4 | a0003c0005t0002g0050 a0003c0005t0002g0051 a0003c0005t0002g0073 others(1): Show |
4 | HG02257.hp1 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+7696G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037989 | |||||||
chr13:21037992 | G | A | 3 | a0003c0032t0016g0313 a0004c0004t0004g0296 a0004c0004t0014g0297 |
3 | HG02647.hp2 HG03540.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.342+7693C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037992 | |||||||
chr13:21038010 | C | T | 24 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(21): Show |
24 | HG00597.hp2 HG00642.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.342+7675G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038010 | |||||||
chr13:21038020 | C | T | 28 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(25): Show |
28 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.342+7665G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038020 | |||||||
chr13:21038066 | A | G | 123 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(120): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.342+7619T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038066 | |||||||
chr13:21038086 | A | C | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+7599T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038086 | |||||||
chr13:21038113 | G | A | 163 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(160): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.342+7572C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038113 | |||||||
chr13:21038169 | G | A | 1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.342+7516C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038169 | |||||||
chr13:21038322 | G | A | 1 | a0003c0005t0015g0071 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.342+7363C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038322 | |||||||
chr13:21038336 | T | C | 3 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 |
3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+7349A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038336 | |||||||
chr13:21038425 | A | T | 3 | a0002c0002t0003g0106 a0002c0002t0003g0117 a0002c0002t0003g0123 |
3 | NA18973.hp2 NA18979.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.342+7260T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038425 | |||||||
chr13:21038515 | C | T | 1 | a0002c0006t0004g0025 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.342+7170G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038515 | |||||||
chr13:21038544 | T | C | 6 | a0003c0008t0009g0292 a0003c0008t0009g0294 a0004c0004t0019g0028 others(3): Show |
6 | HG01433.hp2 HG02258.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+7141A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038544 | |||||||
chr13:21038652 | G | A | 134 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(131): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.342+7033C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038652 | |||||||
chr13:21038742 | C | T | 2 | a0003c0003t0002g0019 a0003c0003t0002g0021 |
2 | HG00642.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.342+6943G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038742 | |||||||
chr13:21038904 | C | T | 7 | a0003c0008t0009g0088 a0003c0009t0008g0307 a0003c0009t0009g0306 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+6781G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038904 | |||||||
chr13:21038920 | T | C | 270 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(267): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.342+6765A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038920 | |||||||
chr13:21038924 | G | C | 3 | a0003c0003t0004g0257 a0003c0003t0025g0285 a0003c0008t0046g0286 |
3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+6761C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038924 | |||||||
chr13:21038965 | T | C | 23 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(20): Show |
23 | HG00597.hp2 HG00642.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.342+6720A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038965 | |||||||
chr13:21038965 | T | G | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+6720A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038965 | |||||||
chr13:21038986 | C | G | 24 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(21): Show |
24 | HG00597.hp2 HG00642.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.342+6699G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038986 | |||||||
chr13:21039049 | T | A | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+6636A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039049 | |||||||
chr13:21039130 | T | C | 141 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(138): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.342+6555A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039130 | |||||||
chr13:21039423 | A | G | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+6262T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039423 | |||||||
chr13:21039424 | G | A | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+6261C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039424 | |||||||
chr13:21039425 | A | G | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+6260T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039425 | |||||||
chr13:21039530 | G | C | 1 | a0002c0002t0006g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.342+6155C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039530 | |||||||
chr13:21039659 | A | G | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+6026T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039659 | |||||||
chr13:21039768 | T | G | 1 | a0006c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+5917A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039768 | |||||||
chr13:21039864 | A | C | 10 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(7): Show |
10 | HG00735.hp2 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.342+5821T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039864 | |||||||
chr13:21039941 | C | T | 4 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(1): Show |
5 | HG02451.hp1 HG02895.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+5744G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039941 | |||||||
chr13:21039998 | G | A | 1 | a0003c0008t0009g0294 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.342+5687C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039998 | |||||||
chr13:21040059 | G | C | 1 | a0001c0001t0027g0224 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.342+5626C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040059 | |||||||
chr13:21040073 | CA | C | 6 | a0001c0001t0001g0273 a0002c0002t0003g0095 a0002c0002t0003g0101 others(3): Show |
6 | HG01168.hp1 HG01496.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+5611delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040073 | |||||||
chr13:21040361 | C | T | 162 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.342+5324G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040361 | |||||||
chr13:21040373 | T | C | 7 | a0002c0002t0011g0036 a0003c0009t0026g0031 a0003c0009t0031g0033 others(4): Show |
7 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.342+5312A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040373 | |||||||
chr13:21040376 | C | CA | 28 | a0001c0001t0022g0171 a0002c0006t0004g0014 a0002c0006t0004g0015 others(25): Show |
28 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.342+5308dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040376 | |||||||
chr13:21040376 | C | CAAAAAAA others(5): Show |
1 | a0005c0016t0014g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.342+5297_342+5308d others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040376 | |||||||
chr13:21040376 | C | CAAAAAAA others(6): Show |
1 | a0005c0016t0014g0037 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.342+5296_342+5308d others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040376 | |||||||
chr13:21040388 | A | G | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+5297T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040388 | |||||||
chr13:21040392 | G | A | 11 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(8): Show |
11 | HG00735.hp2 HG02055.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.342+5293C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040392 | |||||||
chr13:21040396 | G | A | 4 | a0003c0003t0025g0285 a0003c0008t0046g0286 a0005c0016t0014g0037 others(1): Show |
4 | HG02055.hp2 HG02630.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+5289C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040396 | |||||||
chr13:21040402 | G | A | 2 | a0003c0003t0025g0285 a0003c0008t0046g0286 |
2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+5283C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040402 | |||||||
chr13:21040416 | T | G | 2 | a0003c0003t0025g0285 a0003c0008t0046g0286 |
2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+5269A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040416 | |||||||
chr13:21040426 | G | T | 8 | a0001c0001t0004g0274 a0001c0001t0006g0168 a0001c0001t0006g0184 others(5): Show |
8 | HG00423.hp1 HG02071.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+5259C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040426 | |||||||
chr13:21040561 | T | G | 7 | a0002c0002t0011g0036 a0003c0009t0026g0031 a0003c0009t0031g0033 others(4): Show |
7 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.342+5124A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040561 | |||||||
chr13:21040587 | C | T | 3 | a0002c0002t0003g0148 a0002c0002t0003g0153 a0002c0002t0024g0152 |
3 | HG02148.hp2 NA19000.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.342+5098G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040587 | |||||||
chr13:21040598 | G | A | 76 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(73): Show |
76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.342+5087C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040598 | |||||||
chr13:21040977 | C | CT | 11 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(8): Show |
11 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.342+4707dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040977 | |||||||
chr13:21041117 | C | T | 1 | a0004c0004t0005g0089 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.342+4568G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21041117 | |||||||
chr13:21041201 | T | A | 1 | a0002c0002t0003g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.342+4484A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21041201 | |||||||
chr13:21041275 | TCC | T | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+4408_342+4409d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21041275 | |||||||
chr13:21041316 | A | G | 12 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(9): Show |
12 | HG00735.hp2 HG02055.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.342+4369T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21041316 | |||||||
chr13:21041346 | T | C | 128 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(125): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.342+4339A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21041346 | |||||||
chr13:21041932 | C | T | 162 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.342+3753G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21041932 | |||||||
chr13:21042004 | A | T | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+3681T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042004 | |||||||
chr13:21042058 | T | A | 8 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(5): Show |
8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+3627A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042058 | |||||||
chr13:21042340 | T | C | 74 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(71): Show |
74 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.342+3345A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042340 | |||||||
chr13:21042793 | C | G | 11 | a0002c0002t0011g0036 a0003c0003t0025g0285 a0003c0008t0046g0286 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+2892G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042793 | |||||||
chr13:21042843 | G | A | 238 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(235): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.342+2842C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042843 | |||||||
chr13:21042857 | G | A | 9 | a0002c0002t0011g0036 a0003c0009t0026g0031 a0003c0009t0031g0033 others(6): Show |
9 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.342+2828C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042857 | |||||||
chr13:21042909 | G | C | 15 | a0003c0003t0004g0298 a0003c0003t0004g0299 a0003c0008t0008g0289 others(12): Show |
15 | HG01433.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.342+2776C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042909 | |||||||
chr13:21042923 | G | C | 1 | a0003c0023t0002g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.342+2762C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042923 | |||||||
chr13:21042938 | T | C | 279 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(276): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.342+2747A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042938 | |||||||
chr13:21042973 | G | A | 6 | a0002c0006t0004g0254 a0004c0004t0005g0004 a0004c0004t0005g0246 others(3): Show |
6 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+2712C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042973 | |||||||
chr13:21042988 | A | C | 76 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(73): Show |
76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.342+2697T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042988 | |||||||
chr13:21042993 | AC | A | 89 | a0001c0001t0001g0090 a0001c0001t0001g0176 a0001c0001t0001g0180 others(86): Show |
91 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.342+2691delG | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042993 | |||||||
chr13:21042994 | C | A | 191 | a0001c0001t0001g0092 a0001c0001t0001g0245 a0001c0001t0001g0247 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.342+2691G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042994 | |||||||
chr13:21043198 | C | T | 1 | a0003c0005t0004g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.342+2487G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043198 | |||||||
chr13:21043220 | C | T | 5 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(2): Show |
6 | HG02451.hp1 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+2465G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043220 | |||||||
chr13:21043248 | G | A | 2 | a0002c0006t0004g0014 a0002c0006t0004g0015 |
2 | NA19064.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.342+2437C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043248 | |||||||
chr13:21043351 | C | G | 4 | a0001c0001t0002g0223 a0001c0001t0002g0225 a0001c0001t0002g0226 others(1): Show |
4 | HG00741.hp1 HG01106.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+2334G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043351 | |||||||
chr13:21043413 | G | T | 257 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.342+2272C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043413 | |||||||
chr13:21043509 | G | A | 8 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(5): Show |
8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+2176C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043509 | |||||||
chr13:21043595 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.342+2090G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043595 | |||||||
chr13:21043688 | G | T | 11 | a0002c0002t0011g0036 a0003c0003t0025g0285 a0003c0008t0046g0286 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+1997C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043688 | |||||||
chr13:21043707 | T | C | 2 | a0003c0003t0025g0285 a0003c0008t0046g0286 |
2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+1978A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043707 | |||||||
chr13:21043839 | G | A | 1 | a0003c0023t0002g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.342+1846C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043839 | |||||||
chr13:21043867 | C | A | 11 | a0002c0002t0011g0036 a0003c0003t0025g0285 a0003c0008t0046g0286 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+1818G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043867 | |||||||
chr13:21043965 | C | T | 11 | a0002c0002t0011g0036 a0003c0003t0025g0285 a0003c0008t0046g0286 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+1720G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043965 | |||||||
chr13:21043998 | G | C | 4 | a0003c0008t0009g0088 a0004c0019t0020g0303 a0004c0019t0020g0304 others(1): Show |
4 | HG01243.hp1 HG01243.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+1687C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043998 | |||||||
chr13:21044024 | T | C | 1 | a0004c0035t0009g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.342+1661A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044024 | |||||||
chr13:21044046 | A | G | 263 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(260): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.342+1639T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044046 | |||||||
chr13:21044262 | G | A | 15 | a0003c0003t0004g0298 a0003c0003t0004g0299 a0003c0008t0008g0289 others(12): Show |
15 | HG01433.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.342+1423C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044262 | |||||||
chr13:21044466 | G | A | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+1219C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044466 | |||||||
chr13:21044689 | G | GGT | 8 | a0002c0024t0023g0040 a0003c0005t0002g0057 a0003c0005t0002g0058 others(5): Show |
8 | HG00639.hp1 HG01243.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+994_342+995dup others(2): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | |||||||
chr13:21044689 | G | GGTGTGTG others(3): Show |
1 | a0004c0015t0018g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.342+986_342+995dup others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | |||||||
chr13:21044689 | GGT | G | 20 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(17): Show |
21 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.342+994_342+995del others(2): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | |||||||
chr13:21044689 | GGTGT | G | 16 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0001g0265 others(13): Show |
16 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.342+992_342+995del others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | |||||||
chr13:21044689 | GGTGTGT | G | 38 | a0001c0001t0001g0195 a0001c0001t0001g0218 a0001c0001t0001g0235 others(35): Show |
38 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.342+990_342+995del others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | |||||||
chr13:21044689 | GGTGTGTG others(1): Show |
G | 96 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(93): Show |
98 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.342+988_342+995del others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | |||||||
chr13:21044689 | GGTGTGTG others(3): Show |
G | 26 | a0001c0001t0001g0245 a0001c0001t0002g0225 a0001c0001t0002g0226 others(23): Show |
26 | HG00280.hp2 HG00438.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.342+986_342+995del others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | |||||||
chr13:21044689 | GGTGTGTG others(5): Show |
G | 74 | a0001c0001t0010g0112 a0001c0001t0010g0162 a0001c0001t0010g0163 others(71): Show |
74 | HG00621.hp1 HG00735.hp2 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.342+984_342+995del others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | |||||||
chr13:21044689 | GGTGTGTG others(7): Show |
G | 2 | a0001c0001t0022g0171 a0002c0002t0003g0146 |
2 | NA18951.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.342+982_342+995del others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | |||||||
chr13:21044689 | GGTGTGTG others(9): Show |
G | 1 | a0002c0002t0003g0098 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.342+980_342+995del others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | |||||||
chr13:21044689 | GGTGTGTG others(13): Show |
G | 1 | a0001c0001t0001g0252 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.342+976_342+995del others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | |||||||
chr13:21044689 | GGTGTGTG others(19): Show |
G | 17 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(14): Show |
17 | HG00642.hp2 HG01358.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.342+970_342+995del others(26): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | |||||||
chr13:21044693 | T | G | 3 | a0003c0009t0026g0031 a0003c0009t0031g0033 a0005c0012t0002g0034 |
3 | HG02723.hp2 HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.342+992A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044693 | |||||||
chr13:21044697 | T | G | 2 | a0002c0002t0011g0036 a0005c0012t0001g0035 |
2 | HG00735.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.342+988A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044697 | |||||||
chr13:21044728 | GTGTGTGT others(4): Show |
G | 1 | a0004c0004t0005g0228 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.342+946_342+956del others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044728 | |||||||
chr13:21044752 | T | C | 1 | a0002c0002t0003g0125 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.342+933A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044752 | |||||||
chr13:21044856 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.342+829A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044856 | |||||||
chr13:21044870 | CA | C | 257 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.342+814delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044870 | |||||||
chr13:21044908 | T | C | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.342+777A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044908 | |||||||
chr13:21044975 | G | A | 4 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(1): Show |
4 | HG00639.hp1 HG02451.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+710C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044975 | |||||||
chr13:21045106 | CTG | C | 162 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.342+577_342+578del others(2): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21045106 | |||||||
chr13:21045331 | C | T | 17 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(14): Show |
17 | HG00642.hp2 HG01358.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.342+354G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21045331 | |||||||
chr13:21045341 | G | A | 15 | a0003c0003t0004g0298 a0003c0003t0004g0299 a0003c0008t0008g0289 others(12): Show |
15 | HG01433.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.342+344C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21045341 | |||||||
chr13:21045360 | CA | C | 4 | a0002c0034t0035g0029 a0003c0032t0016g0313 a0004c0004t0019g0028 others(1): Show |
4 | HG02965.hp1 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+324delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21045360 | |||||||
chr13:21046325 | A | G | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-204-95T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21046325 | |||||||
chr13:21046330 | G | A | 2 | a0003c0003t0025g0285 a0003c0008t0046g0286 |
2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-204-100C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21046330 | |||||||
chr13:21046450 | C | T | 4 | a0001c0001t0001g0231 a0003c0003t0002g0177 a0003c0003t0002g0178 others(1): Show |
4 | HG00423.hp2 NA18952.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-220G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21046450 | |||||||
chr13:21046671 | C | A | 1 | a0001c0001t0001g0221 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-204-441G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21046671 | |||||||
chr13:21046981 | T | C | 4 | a0001c0001t0002g0203 a0001c0001t0013g0187 a0001c0001t0013g0204 others(1): Show |
4 | HG02027.hp2 NA18980.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-751A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21046981 | |||||||
chr13:21047024 | G | A | 1 | a0002c0027t0039g0114 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-204-794C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047024 | |||||||
chr13:21047027 | A | G | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-204-797T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047027 | |||||||
chr13:21047149 | G | A | 8 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(5): Show |
8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-919C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047149 | |||||||
chr13:21047152 | C | A | 1 | a0004c0035t0009g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-204-922G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047152 | |||||||
chr13:21047191 | G | A | 2 | a0002c0002t0003g0153 a0002c0002t0024g0152 |
2 | NA19000.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-204-961C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047191 | |||||||
chr13:21047222 | C | T | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-992G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047222 | |||||||
chr13:21047403 | T | C | 3 | a0003c0009t0008g0307 a0003c0009t0009g0306 a0003c0009t0032g0287 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-204-1173A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047403 | |||||||
chr13:21047419 | C | T | 162 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-204-1189G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047419 | |||||||
chr13:21047482 | T | C | 1 | a0002c0002t0003g0123 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-204-1252A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047482 | |||||||
chr13:21047499 | C | T | 8 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(5): Show |
8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-1269G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047499 | |||||||
chr13:21047645 | G | A | 7 | a0002c0002t0011g0036 a0003c0009t0026g0031 a0003c0009t0031g0033 others(4): Show |
7 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-204-1415C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047645 | |||||||
chr13:21047669 | C | T | 8 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(5): Show |
8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-1439G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047669 | |||||||
chr13:21047806 | T | C | 4 | a0001c0001t0001g0273 a0002c0034t0035g0029 a0004c0004t0019g0028 others(1): Show |
4 | HG01496.hp1 HG02965.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-1576A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047806 | |||||||
chr13:21047840 | G | C | 3 | a0002c0034t0035g0029 a0004c0004t0019g0028 a0004c0004t0028g0027 |
3 | HG02965.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-204-1610C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047840 | |||||||
chr13:21047851 | G | T | 2 | a0004c0019t0020g0303 a0004c0019t0020g0304 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-204-1621C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047851 | |||||||
chr13:21047895 | T | C | 3 | a0002c0034t0035g0029 a0004c0004t0019g0028 a0004c0004t0028g0027 |
3 | HG02965.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-204-1665A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047895 | |||||||
chr13:21047928 | G | A | 19 | a0002c0002t0011g0036 a0002c0002t0011g0281 a0002c0002t0011g0282 others(16): Show |
19 | HG00735.hp1 HG00735.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-204-1698C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047928 | |||||||
chr13:21048082 | T | C | 265 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(262): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-204-1852A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048082 | |||||||
chr13:21048273 | C | T | 2 | a0003c0005t0002g0039 a0003c0005t0002g0052 |
2 | HG00741.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-204-2043G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048273 | |||||||
chr13:21048444 | C | T | 19 | a0002c0002t0011g0036 a0002c0002t0011g0281 a0002c0002t0011g0282 others(16): Show |
19 | HG00735.hp1 HG00735.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-204-2214G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048444 | |||||||
chr13:21048602 | C | T | 1 | a0003c0003t0002g0188 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-204-2372G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048602 | |||||||
chr13:21048613 | T | C | 257 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-204-2383A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048613 | |||||||
chr13:21048706 | G | A | 121 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(118): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-204-2476C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048706 | |||||||
chr13:21048719 | C | T | 11 | a0002c0002t0011g0036 a0003c0003t0025g0285 a0003c0008t0046g0286 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-204-2489G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048719 | |||||||
chr13:21048768 | C | T | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-204-2538G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048768 | |||||||
chr13:21048773 | G | A | 1 | a0007c0020t0009g0003 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-204-2543C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048773 | |||||||
chr13:21048845 | AAAAAATA others(5): Show |
A | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-2627_-204-261 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048845 | |||||||
chr13:21048853 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-204-2623T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048853 | |||||||
chr13:21049139 | T | C | 11 | a0002c0002t0011g0036 a0003c0003t0025g0285 a0003c0008t0046g0286 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-204-2909A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049139 | |||||||
chr13:21049172 | G | A | 2 | a0004c0004t0005g0227 a0004c0004t0005g0228 |
2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-204-2942C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049172 | |||||||
chr13:21049191 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-204-2961C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049191 | |||||||
chr13:21049278 | T | C | 8 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(5): Show |
8 | NA18945.hp1 NA18950.hp2 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-3048A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049278 | |||||||
chr13:21049329 | G | A | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-204-3099C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049329 | |||||||
chr13:21049330 | G | A | 76 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(73): Show |
76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-204-3100C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049330 | |||||||
chr13:21049367 | C | T | 1 | a0001c0001t0022g0171 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-204-3137G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049367 | |||||||
chr13:21049622 | C | T | 238 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(235): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.-204-3392G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049622 | |||||||
chr13:21049636 | A | G | 2 | a0001c0001t0006g0182 a0001c0001t0012g0165 |
2 | NA18979.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-204-3406T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049636 | |||||||
chr13:21049644 | A | G | 258 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(255): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-204-3414T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049644 | |||||||
chr13:21049662 | A | G | 1 | a0004c0015t0018g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-204-3432T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049662 | |||||||
chr13:21049694 | G | A | 1 | a0003c0007t0008g0072 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-204-3464C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049694 | |||||||
chr13:21049709 | C | T | 2 | a0003c0003t0025g0285 a0003c0008t0046g0286 |
2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-204-3479G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049709 | |||||||
chr13:21049710 | A | G | 7 | a0002c0002t0011g0036 a0003c0009t0026g0031 a0003c0009t0031g0033 others(4): Show |
7 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-204-3480T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049710 | |||||||
chr13:21049732 | C | A | 15 | a0003c0003t0004g0298 a0003c0003t0004g0299 a0003c0008t0008g0289 others(12): Show |
15 | HG01433.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-204-3502G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049732 | |||||||
chr13:21049849 | T | C | 121 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(118): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-204-3619A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049849 | |||||||
chr13:21049872 | G | A | 2 | a0003c0003t0025g0285 a0003c0008t0046g0286 |
2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-204-3642C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049872 | |||||||
chr13:21049877 | T | C | 1 | a0004c0004t0005g0267 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-204-3647A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049877 | |||||||
chr13:21049938 | C | G | 2 | a0002c0002t0003g0116 a0002c0002t0003g0134 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-204-3708G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049938 | |||||||
chr13:21049973 | T | C | 11 | a0002c0002t0011g0036 a0003c0003t0025g0285 a0003c0008t0046g0286 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-204-3743A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049973 | |||||||
chr13:21049974 | A | G | 1 | a0003c0009t0009g0306 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-204-3744T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049974 | |||||||
chr13:21050027 | G | A | 2 | a0003c0005t0002g0069 a0003c0005t0002g0070 |
2 | HG01167.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.-204-3797C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050027 | |||||||
chr13:21050110 | ACT | A | 9 | a0002c0002t0011g0036 a0003c0009t0026g0031 a0003c0009t0031g0033 others(6): Show |
9 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-204-3882_-204-388 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050110 | |||||||
chr13:21050119 | C | CATAG | 4 | a0003c0009t0026g0031 a0003c0009t0031g0033 a0005c0012t0002g0030 others(1): Show |
4 | HG02723.hp2 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-3893_-204-389 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050119 | |||||||
chr13:21050125 | C | CAGACAGA others(49): Show |
1 | a0003c0003t0002g0173 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-204-3896_-204-389 others(60): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | |||||||
chr13:21050125 | C | CAGACAGA others(29): Show |
1 | a0004c0004t0014g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-204-3896_-204-389 others(40): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | |||||||
chr13:21050125 | C | CAGACAGA others(33): Show |
1 | a0004c0004t0004g0296 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-204-3896_-204-389 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | |||||||
chr13:21050125 | C | CAGACAGA others(37): Show |
1 | a0003c0003t0002g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-204-3896_-204-389 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | |||||||
chr13:21050125 | C | CAGACAGA others(21): Show |
5 | a0003c0008t0008g0291 a0003c0008t0009g0292 a0003c0008t0009g0294 others(2): Show |
5 | HG01433.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-204-3896_-204-389 others(32): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | |||||||
chr13:21050125 | C | CAGACAGA others(25): Show |
2 | a0003c0008t0008g0289 a0004c0004t0019g0290 |
2 | HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-204-3896_-204-389 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | |||||||
chr13:21050125 | C | CAGAT | 7 | a0003c0005t0002g0039 a0003c0005t0002g0050 a0003c0005t0002g0051 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-204-3899_-204-389 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | |||||||
chr13:21050125 | C | T | 9 | a0002c0002t0011g0036 a0003c0009t0026g0031 a0003c0009t0031g0033 others(6): Show |
9 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-204-3895G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | |||||||
chr13:21050125 | CAGAT | C | 3 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 |
3 | HG02451.hp2 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-204-3899_-204-389 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | |||||||
chr13:21050129 | T | C | 226 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0180 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.-204-3899A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050129 | |||||||
chr13:21050133 | T | C | 30 | a0002c0002t0003g0124 a0002c0006t0004g0014 a0002c0006t0004g0015 others(27): Show |
30 | HG00642.hp2 HG01074.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-204-3903A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050133 | |||||||
chr13:21050137 | T | C | 1 | a0002c0006t0004g0024 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-204-3907A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050137 | |||||||
chr13:21050139 | G | C | 1 | a0003c0003t0002g0173 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-204-3909C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050139 | |||||||
chr13:21050143 | G | C | 6 | a0003c0003t0002g0172 a0003c0003t0002g0173 a0003c0003t0025g0285 others(3): Show |
6 | HG01099.hp2 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-204-3913C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050143 | |||||||
chr13:21050147 | G | C | 13 | a0003c0003t0002g0172 a0003c0003t0002g0173 a0003c0003t0025g0285 others(10): Show |
13 | HG01099.hp2 HG01433.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-204-3917C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(13): Show |
2 | a0002c0002t0011g0036 a0005c0012t0001g0035 |
2 | HG00735.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(24): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(25): Show |
1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(29): Show |
4 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0235 others(1): Show |
4 | NA19011.hp2 NA19084.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(40): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(33): Show |
1 | a0001c0001t0001g0222 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(17): Show |
2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(28): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(25): Show |
1 | a0001c0001t0001g0272 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(29): Show |
3 | a0001c0001t0001g0218 a0001c0001t0001g0277 a0002c0002t0003g0142 |
3 | HG00438.hp2 HG02056.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(40): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(33): Show |
1 | a0004c0004t0045g0312 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(41): Show |
2 | a0002c0002t0003g0095 a0002c0002t0003g0125 |
2 | HG03017.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(25): Show |
1 | a0001c0001t0001g0207 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(29): Show |
10 | a0001c0001t0001g0245 a0001c0001t0001g0252 a0002c0006t0004g0254 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(40): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(33): Show |
5 | a0001c0001t0001g0270 a0002c0002t0003g0098 a0003c0003t0007g0310 others(2): Show |
5 | HG01074.hp1 HG01257.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(37): Show |
9 | a0001c0001t0001g0219 a0002c0002t0003g0148 a0002c0002t0003g0149 others(6): Show |
9 | HG02015.hp2 HG02148.hp2 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(41): Show |
7 | a0001c0001t0001g0278 a0001c0001t0017g0130 a0001c0001t0017g0131 others(4): Show |
7 | HG01361.hp1 HG02074.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(25): Show |
1 | a0002c0002t0003g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(29): Show |
2 | a0001c0001t0001g0206 a0001c0001t0001g0261 |
2 | HG00738.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(40): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(33): Show |
10 | a0001c0001t0001g0092 a0001c0001t0001g0262 a0001c0001t0001g0264 others(7): Show |
10 | HG01106.hp1 HG01255.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(37): Show |
8 | a0001c0001t0001g0269 a0002c0002t0003g0138 a0002c0002t0003g0140 others(5): Show |
8 | HG01433.hp1 HG02300.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(41): Show |
15 | a0001c0001t0001g0271 a0001c0001t0010g0112 a0002c0002t0003g0094 others(12): Show |
15 | HG00621.hp1 HG01928.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(45): Show |
11 | a0002c0002t0003g0116 a0002c0002t0003g0117 a0002c0002t0003g0120 others(8): Show |
11 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(56): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(49): Show |
1 | a0002c0002t0003g0124 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(60): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(33): Show |
29 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(26): Show |
29 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(37): Show |
8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0034g0214 others(5): Show |
8 | HG00642.hp2 HG02683.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(41): Show |
7 | a0001c0001t0043g0139 a0002c0002t0011g0281 a0002c0006t0004g0217 others(4): Show |
7 | HG02809.hp1 HG02965.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(45): Show |
14 | a0001c0001t0003g0161 a0002c0002t0003g0101 a0002c0002t0003g0102 others(11): Show |
14 | HG01168.hp1 HG01358.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(56): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(49): Show |
8 | a0001c0001t0010g0162 a0001c0001t0010g0163 a0002c0002t0003g0115 others(5): Show |
8 | HG01261.hp1 HG01496.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(60): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(57): Show |
1 | a0003c0003t0007g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(68): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(33): Show |
3 | a0001c0001t0002g0002 a0001c0001t0002g0166 a0002c0002t0010g0279 |
4 | NA19004.hp2 NA19065.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(37): Show |
18 | a0001c0001t0001g0231 a0001c0001t0001g0237 a0001c0001t0001g0238 others(15): Show |
19 | HG00280.hp1 HG00423.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(41): Show |
12 | a0001c0001t0001g0209 a0001c0001t0001g0244 a0002c0006t0004g0014 others(9): Show |
12 | HG00597.hp2 HG02148.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(45): Show |
9 | a0001c0001t0001g0215 a0001c0001t0002g0216 a0002c0006t0004g0169 others(6): Show |
9 | HG01081.hp1 HG01081.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(56): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(49): Show |
4 | a0001c0001t0047g0100 a0002c0002t0011g0283 a0002c0002t0040g0143 others(1): Show |
4 | HG00735.hp2 NA18994.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(60): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(53): Show |
2 | a0002c0002t0003g0154 a0003c0009t0008g0307 |
2 | HG02083.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(64): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(57): Show |
1 | a0006c0013t0007g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(68): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(37): Show |
1 | a0001c0001t0022g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(41): Show |
14 | a0001c0001t0001g0090 a0001c0001t0001g0176 a0001c0001t0001g0180 others(11): Show |
14 | HG01106.hp2 HG01109.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(45): Show |
1 | a0002c0006t0004g0018 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(56): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(49): Show |
1 | a0002c0006t0004g0022 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(60): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(53): Show |
2 | a0001c0001t0010g0099 a0003c0009t0032g0287 |
2 | HG02258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(64): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(41): Show |
4 | a0002c0006t0004g0164 a0003c0003t0002g0011 a0003c0003t0002g0017 others(1): Show |
4 | HG01074.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(45): Show |
2 | a0004c0004t0001g0300 a0004c0004t0005g0089 |
2 | HG01516.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(56): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | G | GATAGATA others(57): Show |
1 | a0003c0009t0009g0306 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(68): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | GATAC | G | 5 | a0001c0022t0004g0010 a0002c0024t0023g0040 a0003c0005t0002g0039 others(2): Show |
5 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-3921_-204-391 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050147 | GATACATA others(5): Show |
G | 1 | a0004c0015t0018g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-204-3929_-204-391 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | |||||||
chr13:21050175 | G | C | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-204-3945C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050175 | |||||||
chr13:21050199 | AG | A | 4 | a0001c0010t0015g0006 a0002c0017t0006g0007 a0003c0005t0015g0008 others(1): Show |
4 | NA18951.hp2 NA18986.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.-204-3970delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050199 | |||||||
chr13:21050227 | G | T | 8 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(5): Show |
8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-3997C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050227 | |||||||
chr13:21050242 | C | T | 123 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(120): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-204-4012G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050242 | |||||||
chr13:21050254 | A | G | 9 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(6): Show |
9 | HG00639.hp1 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-204-4024T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050254 | |||||||
chr13:21050255 | T | C | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-204-4025A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050255 | |||||||
chr13:21050361 | G | GA | 76 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(73): Show |
76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-204-4132dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050361 | |||||||
chr13:21050531 | T | C | 1 | a0004c0015t0018g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-204-4301A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050531 | |||||||
chr13:21050604 | C | T | 8 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(5): Show |
8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-4374G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050604 | |||||||
chr13:21050631 | A | G | 257 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-204-4401T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050631 | |||||||
chr13:21050748 | G | A | 1 | a0004c0015t0005g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-204-4518C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050748 | |||||||
chr13:21050869 | G | T | 4 | a0003c0003t0004g0298 a0003c0003t0004g0299 a0004c0004t0004g0296 others(1): Show |
4 | HG02647.hp2 HG03486.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-204-4639C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050869 | |||||||
chr13:21050929 | C | T | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-204-4699G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050929 | |||||||
chr13:21050944 | G | A | 7 | a0001c0001t0017g0130 a0001c0001t0017g0131 a0002c0002t0003g0126 others(4): Show |
7 | NA18946.hp1 NA18959.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.-204-4714C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050944 | |||||||
chr13:21051042 | T | C | 2 | a0004c0004t0005g0227 a0004c0004t0005g0228 |
2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-204-4812A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051042 | |||||||
chr13:21051052 | T | C | 11 | a0002c0002t0011g0036 a0003c0003t0025g0285 a0003c0008t0046g0286 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-204-4822A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051052 | |||||||
chr13:21051087 | C | A | 26 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(23): Show |
26 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.-204-4857G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051087 | |||||||
chr13:21051092 | G | A | 11 | a0002c0002t0011g0036 a0003c0003t0025g0285 a0003c0008t0046g0286 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-204-4862C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051092 | |||||||
chr13:21051146 | G | C | 4 | a0001c0011t0001g0001 a0001c0011t0001g0081 a0001c0011t0001g0082 others(1): Show |
5 | HG02451.hp1 HG02895.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-4916C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051146 | |||||||
chr13:21051148 | A | G | 8 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(5): Show |
8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-4918T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051148 | |||||||
chr13:21051267 | G | A | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-5037C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051267 | |||||||
chr13:21051288 | T | G | 1 | a0006c0013t0002g0026 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-204-5058A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051288 | |||||||
chr13:21051315 | A | G | 8 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(5): Show |
8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-5085T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051315 | |||||||
chr13:21051334 | C | T | 121 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(118): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-204-5104G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051334 | |||||||
chr13:21051382 | A | G | 5 | a0003c0009t0008g0307 a0003c0009t0009g0306 a0003c0009t0016g0305 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-5152T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051382 | |||||||
chr13:21051535 | T | C | 2 | a0003c0003t0002g0170 a0003c0003t0002g0229 |
2 | HG01070.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-204-5305A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051535 | |||||||
chr13:21051566 | C | T | 5 | a0003c0007t0008g0046 a0003c0007t0008g0047 a0003c0007t0008g0048 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-5336G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051566 | |||||||
chr13:21051739 | G | C | 8 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(5): Show |
8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-5509C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051739 | |||||||
chr13:21051778 | G | A | 8 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(5): Show |
8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-5548C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051778 | |||||||
chr13:21051792 | CTAAAAGT others(7): Show |
C | 1 | a0001c0001t0022g0171 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-204-5576_-204-556 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051792 | |||||||
chr13:21051865 | GA | G | 76 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(73): Show |
76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-204-5636delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051865 | |||||||
chr13:21051920 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-204-5690C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051920 | |||||||
chr13:21051955 | T | A | 1 | a0002c0002t0024g0156 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-204-5725A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051955 | |||||||
chr13:21052013 | G | A | 14 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(11): Show |
14 | HG00738.hp1 HG01074.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.-204-5783C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052013 | |||||||
chr13:21052348 | C | G | 5 | a0003c0009t0008g0307 a0003c0009t0009g0306 a0003c0009t0016g0305 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-6118G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052348 | |||||||
chr13:21052734 | A | G | 36 | a0002c0002t0011g0036 a0002c0002t0011g0281 a0002c0002t0011g0282 others(33): Show |
36 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-204-6504T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052734 | |||||||
chr13:21052773 | GTGCCTGC others(3): Show |
G | 21 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(18): Show |
21 | HG00642.hp2 HG01358.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.-204-6553_-204-654 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052773 | |||||||
chr13:21052795 | T | C | 2 | a0004c0004t0004g0296 a0004c0004t0014g0297 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-204-6565A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052795 | |||||||
chr13:21052894 | G | A | 1 | a0003c0005t0002g0045 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-204-6664C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052894 | |||||||
chr13:21052947 | G | C | 257 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-204-6717C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052947 | |||||||
chr13:21052988 | G | A | 221 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(218): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-204-6758C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052988 | |||||||
chr13:21053041 | C | G | 20 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(17): Show |
20 | HG00642.hp2 HG01358.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.-204-6811G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053041 | |||||||
chr13:21053213 | A | G | 36 | a0002c0002t0011g0036 a0002c0002t0011g0281 a0002c0002t0011g0282 others(33): Show |
36 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-204-6983T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053213 | |||||||
chr13:21053220 | T | A | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-204-6990A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053220 | |||||||
chr13:21053233 | C | CA | 59 | a0001c0001t0001g0092 a0001c0001t0001g0231 a0001c0001t0001g0235 others(56): Show |
60 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-204-7004dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053233 | |||||||
chr13:21053233 | CA | C | 88 | a0001c0001t0002g0166 a0001c0001t0003g0161 a0001c0001t0006g0168 others(85): Show |
88 | HG00438.hp2 HG00738.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.-204-7004delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053233 | |||||||
chr13:21053414 | C | T | 1 | a0004c0004t0028g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-204-7184G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053414 | |||||||
chr13:21053425 | T | C | 221 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(218): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-204-7195A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053425 | |||||||
chr13:21053439 | G | A | 1 | a0006c0013t0007g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-204-7209C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053439 | |||||||
chr13:21053446 | G | A | 2 | a0003c0003t0025g0285 a0003c0008t0046g0286 |
2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-204-7216C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053446 | |||||||
chr13:21053492 | C | T | 2 | a0004c0004t0005g0288 a0004c0004t0005g0309 |
2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-204-7262G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053492 | |||||||
chr13:21053503 | G | A | 1 | a0004c0015t0005g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-204-7273C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053503 | |||||||
chr13:21053518 | A | C | 1 | a0002c0002t0003g0138 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-204-7288T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053518 | |||||||
chr13:21053716 | A | G | 257 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-204-7486T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053716 | |||||||
chr13:21053748 | A | C | 4 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
4 | NA18945.hp1 NA18950.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-7518T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053748 | |||||||
chr13:21053868 | G | A | 25 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(22): Show |
25 | HG00642.hp2 HG00735.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.-205+7478C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053868 | |||||||
chr13:21053930 | C | T | 263 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(260): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-205+7416G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053930 | |||||||
chr13:21053935 | G | C | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205+7411C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053935 | |||||||
chr13:21053948 | T | G | 1 | a0001c0001t0004g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-205+7398A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053948 | |||||||
chr13:21053949 | G | T | 1 | a0001c0001t0004g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-205+7397C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053949 | |||||||
chr13:21053952 | T | G | 1 | a0001c0001t0004g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-205+7394A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053952 | |||||||
chr13:21053955 | G | C | 22 | a0001c0001t0003g0161 a0001c0001t0010g0162 a0001c0001t0010g0163 others(19): Show |
22 | HG00438.hp2 HG02015.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-205+7391C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053955 | |||||||
chr13:21053992 | T | C | 2 | a0002c0002t0003g0157 a0002c0002t0003g0158 |
2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-205+7354A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053992 | |||||||
chr13:21054026 | G | A | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205+7320C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054026 | |||||||
chr13:21054142 | T | C | 262 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(259): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.-205+7204A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054142 | |||||||
chr13:21054505 | C | A | 11 | a0002c0002t0011g0036 a0003c0003t0025g0285 a0003c0008t0046g0286 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-205+6841G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054505 | |||||||
chr13:21054588 | C | T | 11 | a0002c0002t0011g0036 a0003c0003t0025g0285 a0003c0008t0046g0286 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-205+6758G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054588 | |||||||
chr13:21054661 | C | T | 232 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-205+6685G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054661 | |||||||
chr13:21054671 | T | C | 2 | a0003c0003t0025g0285 a0003c0008t0046g0286 |
2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-205+6675A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054671 | |||||||
chr13:21054734 | T | TAAACAGA | 37 | a0002c0002t0011g0036 a0002c0002t0011g0281 a0002c0002t0011g0282 others(34): Show |
37 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.-205+6611_-205+661 others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054734 | |||||||
chr13:21054734 | T | TGAACAGA | 221 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(218): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-205+6611_-205+661 others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054734 | |||||||
chr13:21054803 | G | T | 257 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-205+6543C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054803 | |||||||
chr13:21054804 | T | G | 221 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(218): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-205+6542A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054804 | |||||||
chr13:21054860 | T | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG01496.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-205+6486A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054860 | |||||||
chr13:21054884 | G | C | 8 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(5): Show |
8 | NA18945.hp1 NA18950.hp2 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-205+6462C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054884 | |||||||
chr13:21054896 | A | T | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6450T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054896 | |||||||
chr13:21054897 | C | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6449G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054897 | |||||||
chr13:21054899 | A | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6447T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054899 | |||||||
chr13:21054901 | C | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6445G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054901 | |||||||
chr13:21054903 | G | C | 1 | a0001c0030t0001g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-205+6443C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054903 | |||||||
chr13:21054910 | T | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6436A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054910 | |||||||
chr13:21054912 | T | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6434A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054912 | |||||||
chr13:21054915 | T | C | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6431A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054915 | |||||||
chr13:21054917 | T | C | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6429A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054917 | |||||||
chr13:21054918 | C | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6428G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054918 | |||||||
chr13:21054924 | C | A | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6422G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054924 | |||||||
chr13:21054925 | C | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6421G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054925 | |||||||
chr13:21054926 | C | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6420G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054926 | |||||||
chr13:21054927 | A | T | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6419T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054927 | |||||||
chr13:21054928 | C | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6418G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054928 | |||||||
chr13:21054929 | C | A | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6417G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054929 | |||||||
chr13:21054930 | A | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6416T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054930 | |||||||
chr13:21054931 | T | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6415A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054931 | |||||||
chr13:21054937 | G | C | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6409C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054937 | |||||||
chr13:21054939 | C | T | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6407G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054939 | |||||||
chr13:21054966 | G | T | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6380C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054966 | |||||||
chr13:21054967 | T | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6379A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054967 | |||||||
chr13:21054968 | C | T | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6378G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054968 | |||||||
chr13:21054986 | T | C | 25 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(22): Show |
25 | HG00642.hp2 HG00735.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.-205+6360A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054986 | |||||||
chr13:21054987 | G | GT | 25 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(22): Show |
25 | HG00642.hp2 HG00735.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.-205+6358_-205+635 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054987 | |||||||
chr13:21055063 | T | C | 1 | a0004c0015t0018g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-205+6283A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055063 | |||||||
chr13:21055064 | A | G | 1 | a0003c0036t0009g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-205+6282T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055064 | |||||||
chr13:21055065 | G | A | 219 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.-205+6281C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055065 | |||||||
chr13:21055238 | A | G | 11 | a0002c0002t0011g0036 a0003c0003t0025g0285 a0003c0008t0046g0286 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-205+6108T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055238 | |||||||
chr13:21055250 | C | T | 257 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-205+6096G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055250 | |||||||
chr13:21055271 | A | G | 2 | a0004c0004t0019g0028 a0004c0004t0028g0027 |
2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-205+6075T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055271 | |||||||
chr13:21055308 | TA | T | 220 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-205+6037delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055308 | |||||||
chr13:21055381 | C | T | 1 | a0002c0002t0003g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-205+5965G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055381 | |||||||
chr13:21055724 | C | T | 17 | a0002c0006t0004g0014 a0002c0006t0004g0015 a0002c0006t0004g0018 others(14): Show |
17 | HG00642.hp2 HG01358.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.-205+5622G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055724 | |||||||
chr13:21055810 | A | C | 1 | a0001c0001t0004g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-205+5536T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055810 | |||||||
chr13:21055844 | C | T | 25 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(22): Show |
25 | HG00642.hp2 HG00735.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.-205+5502G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055844 | |||||||
chr13:21055901 | T | C | 1 | a0002c0002t0006g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-205+5445A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055901 | |||||||
chr13:21055997 | G | A | 31 | a0001c0001t0001g0092 a0001c0001t0001g0245 a0001c0001t0001g0247 others(28): Show |
31 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.-205+5349C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055997 | |||||||
chr13:21056071 | G | T | 76 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(73): Show |
76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+5275C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056071 | |||||||
chr13:21056096 | T | C | 1 | a0003c0036t0009g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-205+5250A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056096 | |||||||
chr13:21056131 | T | C | 76 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(73): Show |
76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+5215A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056131 | |||||||
chr13:21056150 | G | C | 3 | a0002c0034t0035g0029 a0004c0004t0019g0028 a0004c0004t0028g0027 |
3 | HG02965.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-205+5196C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056150 | |||||||
chr13:21056153 | G | A | 76 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(73): Show |
76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+5193C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056153 | |||||||
chr13:21056276 | T | C | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-205+5070A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056276 | |||||||
chr13:21056286 | G | A | 76 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(73): Show |
76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+5060C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056286 | |||||||
chr13:21056409 | T | C | 1 | a0003c0023t0002g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-205+4937A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056409 | |||||||
chr13:21056765 | G | C | 1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-205+4581C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056765 | |||||||
chr13:21056850 | A | G | 257 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(254): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-205+4496T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056850 | |||||||
chr13:21056927 | C | T | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-205+4419G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056927 | |||||||
chr13:21057011 | A | G | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205+4335T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057011 | |||||||
chr13:21057041 | C | T | 1 | a0002c0002t0003g0094 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-205+4305G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057041 | |||||||
chr13:21057060 | G | A | 76 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(73): Show |
76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+4286C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057060 | |||||||
chr13:21057105 | C | A | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205+4241G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057105 | |||||||
chr13:21057359 | C | G | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205+3987G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057359 | |||||||
chr13:21057564 | C | T | 2 | a0003c0003t0025g0285 a0003c0008t0046g0286 |
2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-205+3782G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057564 | |||||||
chr13:21057635 | T | TA | 100 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(97): Show |
100 | HG00438.hp2 HG00621.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.-205+3710dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057635 | |||||||
chr13:21057636 | A | T | 120 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(117): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-205+3710T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057636 | |||||||
chr13:21057644 | A | T | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-205+3702T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057644 | |||||||
chr13:21057669 | G | A | 5 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(2): Show |
5 | HG00639.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-205+3677C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057669 | |||||||
chr13:21057757 | G | C | 7 | a0002c0002t0011g0036 a0003c0009t0026g0031 a0003c0009t0031g0033 others(4): Show |
7 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-205+3589C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057757 | |||||||
chr13:21057805 | TA | T | 310 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(307): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.-205+3540delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057805 | |||||||
chr13:21057833 | G | A | 3 | a0002c0002t0010g0279 a0002c0028t0041g0280 a0003c0008t0009g0088 |
3 | HG01243.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-205+3513C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057833 | |||||||
chr13:21057991 | C | T | 5 | a0002c0014t0018g0041 a0002c0014t0018g0042 a0002c0014t0038g0043 others(2): Show |
5 | HG00639.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-205+3355G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057991 | |||||||
chr13:21058089 | G | A | 145 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(142): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-205+3257C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058089 | |||||||
chr13:21058188 | T | C | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-205+3158A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058188 | |||||||
chr13:21058333 | C | T | 11 | a0002c0002t0011g0036 a0003c0003t0025g0285 a0003c0008t0046g0286 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-205+3013G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058333 | |||||||
chr13:21058596 | T | C | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-205+2750A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058596 | |||||||
chr13:21058605 | C | T | 2 | a0004c0019t0020g0303 a0004c0019t0020g0304 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-205+2741G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058605 | |||||||
chr13:21058772 | G | T | 76 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(73): Show |
76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+2574C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058772 | |||||||
chr13:21058941 | G | GA | 12 | a0001c0011t0001g0086 a0002c0002t0011g0036 a0003c0003t0025g0285 others(9): Show |
12 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-205+2404dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058941 | |||||||
chr13:21058979 | T | C | 1 | a0001c0001t0001g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-205+2367A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058979 | |||||||
chr13:21059013 | A | G | 1 | a0003c0005t0002g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-205+2333T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059013 | |||||||
chr13:21059166 | T | G | 1 | a0002c0002t0003g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-205+2180A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059166 | |||||||
chr13:21059170 | T | C | 2 | a0005c0016t0014g0037 a0005c0016t0014g0038 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-205+2176A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059170 | |||||||
chr13:21059233 | T | A | 76 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(73): Show |
76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+2113A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059233 | |||||||
chr13:21059308 | A | G | 178 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.-205+2038T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059308 | |||||||
chr13:21059345 | C | T | 7 | a0002c0002t0011g0036 a0003c0009t0026g0031 a0003c0009t0031g0033 others(4): Show |
7 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-205+2001G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059345 | |||||||
chr13:21059411 | T | C | 86 | a0001c0001t0003g0161 a0001c0001t0010g0099 a0001c0001t0010g0112 others(83): Show |
86 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.-205+1935A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059411 | |||||||
chr13:21059458 | G | A | 1 | a0001c0001t0003g0161 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-205+1888C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059458 | |||||||
chr13:21059506 | A | G | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1840T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059506 | |||||||
chr13:21059508 | A | C | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1838T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059508 | |||||||
chr13:21059516 | A | ACAGGAGA others(15): Show |
1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1829_-205+183 others(26): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059516 | |||||||
chr13:21059518 | C | G | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1828G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059518 | |||||||
chr13:21059542 | C | T | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1804G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059542 | |||||||
chr13:21059545 | A | T | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1801T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059545 | |||||||
chr13:21059553 | C | G | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1793G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059553 | |||||||
chr13:21059555 | A | T | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1791T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059555 | |||||||
chr13:21059679 | T | G | 2 | a0001c0001t0010g0162 a0001c0001t0010g0163 |
2 | NA18971.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-205+1667A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059679 | |||||||
chr13:21059686 | T | C | 2 | a0004c0019t0020g0303 a0004c0019t0020g0304 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-205+1660A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059686 | |||||||
chr13:21059720 | C | G | 9 | a0002c0002t0011g0036 a0003c0009t0026g0031 a0003c0009t0031g0033 others(6): Show |
9 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-205+1626G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059720 | |||||||
chr13:21060047 | AG | A | 5 | a0003c0009t0008g0307 a0003c0009t0009g0306 a0003c0009t0016g0305 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-205+1298delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060047 | |||||||
chr13:21060193 | C | G | 167 | a0001c0001t0001g0176 a0001c0001t0001g0180 a0001c0001t0001g0181 others(164): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.-205+1153G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060193 | |||||||
chr13:21060243 | C | T | 1 | a0003c0009t0032g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-205+1103G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060243 | |||||||
chr13:21060324 | G | T | 2 | a0003c0003t0025g0285 a0003c0008t0046g0286 |
2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-205+1022C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060324 | |||||||
chr13:21060353 | A | C | 1 | a0001c0022t0004g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-205+993T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060353 | |||||||
chr13:21060504 | C | T | 1 | a0003c0023t0002g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-205+842G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060504 | |||||||
chr13:21060585 | C | T | 3 | a0001c0010t0015g0006 a0002c0017t0006g0007 a0003c0005t0015g0008 |
3 | NA18951.hp2 NA18986.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-205+761G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060585 | |||||||
chr13:21060613 | G | C | 82 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0003g0161 others(79): Show |
82 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.-205+733C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060613 | |||||||
chr13:21060631 | A | G | 82 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0003g0161 others(79): Show |
82 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.-205+715T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060631 | |||||||
chr13:21060657 | G | C | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-205+689C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060657 | |||||||
chr13:21060676 | C | G | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-205+670G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060676 | |||||||
chr13:21060844 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG02056.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-205+502C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060844 | |||||||
chr13:21060861 | G | A | 2 | a0002c0002t0010g0279 a0002c0028t0041g0280 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-205+485C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060861 | |||||||
chr13:21060910 | T | G | 225 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0176 others(222): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-205+436A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060910 | |||||||
chr13:21060926 | G | A | 4 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(1): Show |
4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205+420C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060926 | |||||||
chr13:21060973 | G | A | 1 | a0004c0004t0005g0309 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-205+373C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060973 | |||||||
chr13:21061004 | G | A | 29 | a0002c0002t0011g0281 a0002c0002t0011g0282 a0002c0002t0011g0283 others(26): Show |
29 | HG00735.hp2 HG01243.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.-205+342C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21061004 | |||||||
chr13:21061015 | G | GC | 25 | a0003c0003t0004g0298 a0003c0003t0004g0299 a0003c0003t0025g0285 others(22): Show |
25 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-205+330dupG | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21061015 | |||||||
chr13:21061124 | G | A | 3 | a0003c0003t0007g0310 a0003c0003t0007g0311 a0004c0004t0045g0312 |
3 | HG01257.hp2 HG02738.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-205+222C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21061124 | |||||||
chr13:21061244 | G | C | 1 | a0003c0032t0016g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-205+102C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21061244 | |||||||
chr13:21061321 | C | T | 1 | a0004c0004t0005g0004 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-205+25G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21061321 |