Item | Value |
---|---|
geneid | 9113 |
ensemblid | ENSG00000131023.13 |
hgncid | 6514 |
symbol | LATS1 |
name | large tumor suppressor kinase 1 |
refseq_nuc | NM_004690.4 |
refseq_prot | NP_004681.1 |
ensembl_nuc | ENST00000543571.6 |
ensembl_prot | ENSP00000437550.1 |
mane_status | MANE Select |
chr | chr6 |
start | 149658153 |
end | 149718101 |
strand | - |
ver | v1.2 |
region | chr6:149658153-149718101 |
region5000 | chr6:149653153-149723101 |
regionname0 | LATS1_chr6_149658153_149718101 |
regionname5000 | LATS1_chr6_149653153_149723101 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1130 | 252 | 77 | 36 | 100 | 12 | 25 | 82 | LATS1_chr6_149653153_149723101 | LATS1 | MKRSE others(1125): Show |
chr6 | 149653153 | 149723101 |
a0002 | 0/0 | 1130 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | MKRSE others(1125): Show |
chr6 | 149653153 | 149723101 |
a0003 | 0/0 | 1130 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | MKRSE others(1125): Show |
chr6 | 149653153 | 149723101 |
a0004 | 0/0 | 1130 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | LATS1_chr6_149653153_149723101 | LATS1 | MKRSE others(1125): Show |
chr6 | 149653153 | 149723101 |
a0005 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | MKRSE others(1125): Show |
chr6 | 149653153 | 149723101 |
a0006 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | MKRSE others(1125): Show |
chr6 | 149653153 | 149723101 |
a0007 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | MKRSE others(1125): Show |
chr6 | 149653153 | 149723101 |
a0008 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | MKRSE others(1125): Show |
chr6 | 149653153 | 149723101 |
a0009 | 0/0 | 1130 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | MKRSE others(1125): Show |
chr6 | 149653153 | 149723101 |
a0010 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | MKRSE others(1125): Show |
chr6 | 149653153 | 149723101 |
a0011 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | MKRSE others(1125): Show |
chr6 | 149653153 | 149723101 |
a0012 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | MKRSE others(1125): Show |
chr6 | 149653153 | 149723101 |
a0013 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | MKRSE others(1125): Show |
chr6 | 149653153 | 149723101 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3390 | 130 | 38 | 17 | 58 | 6 | 10 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0001c0002 | 1/0 | 3390 | 117 | 34 | 19 | 42 | 6 | 15 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0001c0004 | 0/0 | 3390 | 4 | 4 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0001c0010 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0002c0003 | 0/0 | 3390 | 7 | 7 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0003c0006 | 0/0 | 3390 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0004c0005 | 0/0 | 3390 | 2 | 0 | 0 | 2 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0005c0016 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0006c0013 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0007c0007 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0008c0009 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0009c0012 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0010c0014 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0011c0008 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0012c0011 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 | ||
a0013c0015 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | ATGAA others(3385): Show |
chr6 | 149653153 | 149723101 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 7363 | 72 | 11 | 12 | 35 | 6 | 7 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7358): Show |
chr6 | 149653153 | 149723101 |
a0001c0001t0004 | 0/0 | 7363 | 26 | 0 | 3 | 20 | 0 | 3 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7358): Show |
chr6 | 149653153 | 149723101 |
a0001c0001t0005 | 0/0 | 7365 | 11 | 11 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7360): Show |
chr6 | 149653153 | 149723101 |
a0001c0001t0006 | 0/0 | 7363 | 8 | 8 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7358): Show |
chr6 | 149653153 | 149723101 |
a0001c0001t0007 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0001t0011 | 0/0 | 7363 | 3 | 1 | 2 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7358): Show |
chr6 | 149653153 | 149723101 |
a0001c0001t0012 | 0/0 | 7363 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7358): Show |
chr6 | 149653153 | 149723101 |
a0001c0001t0016 | 0/0 | 7365 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7360): Show |
chr6 | 149653153 | 149723101 |
a0001c0001t0017 | 0/0 | 7363 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7358): Show |
chr6 | 149653153 | 149723101 |
a0001c0001t0026 | 0/0 | 7363 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7358): Show |
chr6 | 149653153 | 149723101 |
a0001c0001t0028 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0001t0029 | 0/0 | 7362 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0001t0030 | 0/0 | 7365 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7360): Show |
chr6 | 149653153 | 149723101 |
a0001c0002t0002 | 1/0 | 7362 | 65 | 6 | 10 | 37 | 4 | 7 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0002t0003 | 0/0 | 7362 | 24 | 17 | 1 | 1 | 1 | 4 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0002t0008 | 0/0 | 7362 | 7 | 7 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0002t0009 | 0/0 | 7362 | 7 | 0 | 2 | 0 | 1 | 4 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0002t0010 | 0/0 | 7362 | 5 | 1 | 4 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0002t0014 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0002t0015 | 0/0 | 7362 | 2 | 0 | 0 | 2 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0002t0018 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0002t0019 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0002t0020 | 0/0 | 7362 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0002t0022 | 0/0 | 7362 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0002t0024 | 0/0 | 7362 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0002t0025 | 0/0 | 7362 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0001c0004t0012 | 0/0 | 7363 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7358): Show |
chr6 | 149653153 | 149723101 |
a0001c0004t0013 | 0/0 | 7363 | 3 | 3 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7358): Show |
chr6 | 149653153 | 149723101 |
a0001c0010t0023 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0002c0003t0007 | 0/0 | 7362 | 7 | 7 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0003c0006t0002 | 0/0 | 7362 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0004c0005t0003 | 0/0 | 7362 | 2 | 0 | 0 | 2 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0005c0016t0001 | 0/0 | 7363 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7358): Show |
chr6 | 149653153 | 149723101 |
a0006c0013t0004 | 0/0 | 7363 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7358): Show |
chr6 | 149653153 | 149723101 |
a0007c0007t0014 | 0/0 | 7362 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0008c0009t0027 | 0/0 | 7363 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7358): Show |
chr6 | 149653153 | 149723101 |
a0009c0012t0003 | 0/0 | 7362 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0010c0014t0002 | 0/0 | 7362 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0011c0008t0002 | 0/0 | 7362 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0012c0011t0003 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
a0013c0015t0021 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | AGCGG others(7357): Show |
chr6 | 149653153 | 149723101 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0011g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0011g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0016g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0016g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0017g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0026g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0028g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0029g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0030g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0008g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0010g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0010g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0010g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0015g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0015g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0018g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0019g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0020g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0022g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0024g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0025g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0004t0012g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0004t0013g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0004t0013g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0004t0013g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0010t0023g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0003c0006t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0003c0006t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0004c0005t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0004c0005t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0005c0016t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0006c0013t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0007c0007t0014g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0008c0009t0027g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0009c0012t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0010c0014t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0011c0008t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0012c0011t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0013c0015t0021g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0003 | g0057 | EUR | GBR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00140 | hp1 | a0001 | c0002 | t0009 | g0061 | EUR | GBR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0153 | EAS | CHS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00642 | hp1 | a0001 | c0002 | t0009 | g0088 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00642 | hp2 | a0005 | c0016 | t0001 | g0200 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00738 | hp1 | a0001 | c0002 | t0010 | g0125 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0052 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01074 | hp1 | a0006 | c0013 | t0004 | g0171 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01106 | hp1 | a0001 | c0002 | t0022 | g0101 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01109 | hp1 | a0007 | c0007 | t0014 | g0121 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01109 | hp2 | a0001 | c0002 | t0010 | g0005 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0148 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0096 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01175 | hp2 | a0008 | c0009 | t0027 | g0233 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01192 | hp1 | a0001 | c0002 | t0010 | g0005 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01192 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0078 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0084 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01433 | hp1 | a0001 | c0001 | t0011 | g0185 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01433 | hp2 | a0001 | c0002 | t0009 | g0099 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0034 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0093 | EUR | IBS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0108 | EUR | IBS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0094 | EUR | IBS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01884 | hp1 | a0001 | c0001 | t0030 | g0265 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01975 | hp2 | a0001 | c0002 | t0010 | g0122 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0221 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02004 | hp2 | a0001 | c0002 | t0024 | g0124 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0263 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02055 | hp2 | a0001 | c0002 | t0008 | g0030 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02080 | hp1 | a0001 | c0002 | t0003 | g0081 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0170 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02145 | hp2 | a0001 | c0002 | t0008 | g0001 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0253 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02258 | hp2 | a0001 | c0002 | t0003 | g0111 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02273 | hp2 | a0001 | c0001 | t0011 | g0227 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02280 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02451 | hp2 | a0001 | c0002 | t0010 | g0123 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0120 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0240 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02602 | hp1 | a0001 | c0002 | t0003 | g0112 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0208 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02615 | hp1 | a0001 | c0001 | t0012 | g0168 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0260 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02622 | hp2 | a0001 | c0002 | t0003 | g0118 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02630 | hp1 | a0001 | c0002 | t0003 | g0075 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02630 | hp2 | a0001 | c0001 | t0012 | g0169 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02647 | hp1 | a0001 | c0002 | t0003 | g0076 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02647 | hp2 | a0001 | c0002 | t0019 | g0115 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02683 | hp1 | a0009 | c0012 | t0003 | g0056 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0066 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0097 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0137 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02717 | hp2 | a0001 | c0001 | t0016 | g0258 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0241 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02723 | hp2 | a0001 | c0002 | t0003 | g0073 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02886 | hp1 | a0002 | c0003 | t0007 | g0142 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02886 | hp2 | a0001 | c0002 | t0008 | g0028 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02895 | hp1 | a0001 | c0004 | t0013 | g0251 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02895 | hp2 | a0001 | c0002 | t0003 | g0105 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02896 | hp1 | a0001 | c0002 | t0003 | g0106 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0113 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02897 | hp1 | a0001 | c0004 | t0013 | g0250 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0087 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0060 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02922 | hp2 | a0002 | c0003 | t0007 | g0141 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0109 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02970 | hp1 | a0002 | c0003 | t0007 | g0143 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0254 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0138 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0242 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0261 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03195 | hp2 | a0001 | c0004 | t0012 | g0144 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03209 | hp1 | a0001 | c0002 | t0003 | g0046 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03209 | hp2 | a0003 | c0006 | t0002 | g0048 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03225 | hp1 | a0001 | c0002 | t0003 | g0044 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0264 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03453 | hp2 | a0003 | c0006 | t0002 | g0058 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03486 | hp1 | a0001 | c0001 | t0016 | g0259 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03486 | hp2 | a0001 | c0002 | t0008 | g0001 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0116 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03491 | hp1 | a0001 | c0002 | t0009 | g0019 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03492 | hp2 | a0001 | c0002 | t0009 | g0018 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03516 | hp1 | a0001 | c0002 | t0008 | g0026 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03516 | hp2 | a0001 | c0001 | t0028 | g0139 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03540 | hp1 | a0001 | c0002 | t0003 | g0117 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03579 | hp1 | a0002 | c0003 | t0007 | g0135 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0262 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03688 | hp2 | a0001 | c0002 | t0009 | g0095 | SAS | STU | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0020 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03831 | hp1 | a0001 | c0002 | t0009 | g0033 | SAS | BEB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0098 | SAS | BEB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03942 | hp2 | a0001 | c0002 | t0003 | g0103 | SAS | BEB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG04115 | hp1 | a0001 | c0002 | t0003 | g0083 | SAS | STU | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG04115 | hp2 | a0001 | c0002 | t0003 | g0023 | SAS | STU | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0021 | SAS | BEB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0252 | AFR | YRI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18522 | hp2 | a0001 | c0002 | t0003 | g0041 | AFR | YRI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | YRI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0255 | AFR | YRI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18943 | hp1 | a0001 | c0002 | t0025 | g0126 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18944 | hp2 | a0010 | c0014 | t0002 | g0080 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18949 | hp1 | a0001 | c0002 | t0020 | g0071 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18960 | hp1 | a0001 | c0001 | t0017 | g0008 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18961 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18969 | hp2 | a0004 | c0005 | t0003 | g0050 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18995 | hp1 | a0004 | c0005 | t0003 | g0059 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18995 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19009 | hp2 | a0001 | c0002 | t0015 | g0089 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19010 | hp1 | a0001 | c0001 | t0029 | g0248 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0119 | AFR | LWK | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19030 | hp2 | a0001 | c0002 | t0018 | g0014 | AFR | LWK | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19043 | hp1 | a0002 | c0003 | t0007 | g0134 | AFR | LWK | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19043 | hp2 | a0001 | c0002 | t0008 | g0029 | AFR | LWK | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19054 | hp1 | a0001 | c0002 | t0015 | g0035 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19055 | hp1 | a0001 | c0001 | t0026 | g0182 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19087 | hp1 | a0011 | c0008 | t0002 | g0031 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19088 | hp2 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19240 | hp1 | a0002 | c0003 | t0007 | g0140 | AFR | YRI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19240 | hp2 | a0012 | c0011 | t0003 | g0082 | AFR | YRI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | ASW | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA20129 | hp2 | a0001 | c0001 | t0011 | g0184 | AFR | ASW | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | TSI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0102 | EUR | TSI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0243 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02109 | hp2 | a0001 | c0002 | t0008 | g0027 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02486 | hp1 | a0001 | c0002 | t0003 | g0042 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0239 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02559 | hp2 | a0001 | c0002 | t0003 | g0074 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03471 | hp1 | a0001 | c0002 | t0014 | g0010 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03471 | hp2 | a0001 | c0004 | t0013 | g0249 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG06807 | hp1 | a0002 | c0003 | t0007 | g0133 | AFR | USA | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG06807 | hp2 | a0001 | c0010 | t0023 | g0009 | AFR | USA | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA21309 | hp1 | a0013 | c0015 | t0021 | g0011 | AFR | LWK | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA21309 | hp2 | a0001 | c0002 | t0003 | g0043 | AFR | LWK | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0161 | REF | REF | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0091 | REF | REF | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:149676644 | C | T | 1 | a0003 | 2 | HG03209.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.2687G>A | p.Arg896Gln | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 6/8 | 3080/7362 | 2687/3393 | 896/1130 | chr6 | 149676644 | |||
chr6:149676725 | C | T | 1 | a0008 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.2606G>A | p.Arg869Gln | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 6/8 | 2999/7362 | 2606/3393 | 869/1130 | chr6 | 149676725 | |||
chr6:149683150 | C | T | 1 | a0012 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1939G>A | p.Val647Ile | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 2332/7362 | 1939/3393 | 647/1130 | chr6 | 149683150 | |||
chr6:149683603 | G | C | 1 | a0009 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1486C>G | p.Gln496Glu | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 1879/7362 | 1486/3393 | 496/1130 | chr6 | 149683603 | |||
chr6:149684127 | C | T | 1 | a0011 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.962G>A | p.Ser321Asn | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 1355/7362 | 962/3393 | 321/1130 | chr6 | 149684127 | |||
chr6:149684250 | T | C | 1 | a0006 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.839A>G | p.Asn280Ser | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 1232/7362 | 839/3393 | 280/1130 | chr6 | 149684250 | |||
chr6:149684379 | G | T | 1 | a0004 | 2 | NA18969.hp2 NA18995.hp1 |
missense_variant | MODERATE | c.710C>A | p.Pro237Gln | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 1103/7362 | 710/3393 | 237/1130 | chr6 | 149684379 | |||
chr6:149684479 | T | C | 1 | a0002 | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
missense_variant | MODERATE | c.610A>G | p.Ser204Gly | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 1003/7362 | 610/3393 | 204/1130 | chr6 | 149684479 | |||
chr6:149684569 | G | A | 1 | a0010 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.520C>T | p.Arg174Cys | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 913/7362 | 520/3393 | 174/1130 | chr6 | 149684569 | |||
chr6:149695107 | C | T | 1 | a0007 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.463G>A | p.Ala155Thr | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/8 | 856/7362 | 463/3393 | 155/1130 | chr6 | 149695107 | |||
chr6:149701838 | T | C | 1 | a0013 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.289A>G | p.Ser97Gly | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/8 | 682/7362 | 289/3393 | 97/1130 | chr6 | 149701838 | |||
chr6:149701841 | G | A | 1 | a0005 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.286C>T | p.Arg96Trp | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/8 | 679/7362 | 286/3393 | 96/1130 | chr6 | 149701841 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:149662059 | C | T | 1 | a0001c0004 | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.3063G>A | p.Gln1021Gln | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 3456/7362 | 3063/3393 | 1021/1130 | chr6 | 149662059 | |||
chr6:149662080 | G | A | 7 | a0001c0001 a0001c0004 a0002c0003 others(4): Show |
144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
synonymous_variant | LOW | c.3042C>T | p.Asp1014Asp | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 3435/7362 | 3042/3393 | 1014/1130 | chr6 | 149662080 | |||
chr6:149683469 | C | T | 1 | a0001c0010 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.1620G>A | p.Val540Val | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 2013/7362 | 1620/3393 | 540/1130 | chr6 | 149683469 | |||
chr6:149683643 | A | G | 8 | a0001c0001 a0001c0004 a0002c0003 others(5): Show |
145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
synonymous_variant | LOW | c.1446T>C | p.Ser482Ser | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 1839/7362 | 1446/3393 | 482/1130 | chr6 | 149683643 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:149658280 | G | A | 5 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0026 others(2): Show |
77 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3449C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 3449 | chr6 | 149658280 | ||||||
chr6:149658437 | T | C | 1 | a0001c0001t0028 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3292A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 3292 | chr6 | 149658437 | ||||||
chr6:149658547 | A | T | 19 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(16): Show |
143 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*3182T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 3182 | chr6 | 149658547 | ||||||
chr6:149658700 | A | T | 1 | a0001c0002t0009 | 7 | HG00140.hp1 HG00642.hp1 HG01433.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3029T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 3029 | chr6 | 149658700 | ||||||
chr6:149658764 | G | A | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(17): Show |
144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*2965C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2965 | chr6 | 149658764 | ||||||
chr6:149659093 | T | C | 1 | a0001c0001t0016 | 2 | HG02717.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2636A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2636 | chr6 | 149659093 | ||||||
chr6:149659178 | C | T | 1 | a0001c0002t0015 | 2 | NA19009.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2551G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2551 | chr6 | 149659178 | ||||||
chr6:149659317 | A | C | 15 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(12): Show |
133 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*2412T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2412 | chr6 | 149659317 | ||||||
chr6:149659442 | G | C | 4 | a0001c0002t0003 a0004c0005t0003 a0009c0012t0003 others(1): Show |
28 | HG00099.hp1 HG01192.hp2 HG02080.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2287C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2287 | chr6 | 149659442 | ||||||
chr6:149659444 | G | A | 1 | a0001c0002t0022 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2285C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2285 | chr6 | 149659444 | ||||||
chr6:149659591 | A | G | 15 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(12): Show |
133 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*2138T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2138 | chr6 | 149659591 | ||||||
chr6:149660024 | G | A | 1 | a0001c0001t0006 | 8 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1705C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1705 | chr6 | 149660024 | ||||||
chr6:149660024 | G | T | 1 | a0001c0001t0026 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1705C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1705 | chr6 | 149660024 | ||||||
chr6:149660025 | T | A | 1 | a0001c0001t0026 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1704A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1704 | chr6 | 149660025 | ||||||
chr6:149660027 | A | G | 1 | a0001c0001t0026 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1702T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1702 | chr6 | 149660027 | ||||||
chr6:149660122 | T | C | 1 | a0008c0009t0027 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1607A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1607 | chr6 | 149660122 | ||||||
chr6:149660233 | G | A | 1 | a0013c0015t0021 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1496C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1496 | chr6 | 149660233 | ||||||
chr6:149660323 | A | G | 23 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(20): Show |
147 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*1406T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1406 | chr6 | 149660323 | ||||||
chr6:149660518 | T | A | 1 | a0001c0010t0023 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1211A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1211 | chr6 | 149660518 | ||||||
chr6:149660635 | C | T | 1 | a0001c0002t0008 | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1094G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1094 | chr6 | 149660635 | ||||||
chr6:149660828 | A | G | 1 | a0001c0002t0024 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*901T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 901 | chr6 | 149660828 | ||||||
chr6:149661076 | A | G | 1 | a0001c0002t0020 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*653T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 653 | chr6 | 149661076 | ||||||
chr6:149661108 | C | T | 1 | a0001c0002t0019 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*621G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 621 | chr6 | 149661108 | ||||||
chr6:149661115 | T | TG | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(9): Show |
119 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*613dupC | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 613 | chr6 | 149661115 | ||||||
chr6:149661281 | A | G | 15 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(12): Show |
133 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*448T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 448 | chr6 | 149661281 | ||||||
chr6:149661516 | C | T | 1 | a0001c0002t0018 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*213G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 213 | chr6 | 149661516 | ||||||
chr6:149661557 | G | A | 1 | a0001c0001t0011 | 3 | HG01433.hp1 HG02273.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*172C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 172 | chr6 | 149661557 | ||||||
chr6:149702212 | C | G | 9 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(6): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(103): Show |
5_prime_UTR_variant | MODIFIER | c.-86G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/8 | 86 | chr6 | 149702212 | ||||||
chr6:149717856 | G | A | 1 | a0001c0001t0029 | 1 | NA19010.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15730 | chr6 | 149717856 | ||||||
chr6:149717936 | G | A | 1 | a0001c0004t0013 | 3 | HG02895.hp1 HG02897.hp1 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-228C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15810 | chr6 | 149717936 | ||||||
chr6:149717955 | G | A | 2 | a0001c0002t0010 a0001c0002t0024 |
6 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-247C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15829 | chr6 | 149717955 | ||||||
chr6:149718005 | G | C | 1 | a0001c0002t0025 | 1 | NA18943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-297C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15879 | chr6 | 149718005 | ||||||
chr6:149718012 | G | A | 19 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(16): Show |
143 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(140): Show |
5_prime_UTR_variant | MODIFIER | c.-304C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15886 | chr6 | 149718012 | ||||||
chr6:149718068 | C | T | 1 | a0001c0001t0017 | 1 | NA18960.hp1 | 5_prime_UTR_variant | MODIFIER | c.-360G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15942 | chr6 | 149718068 | ||||||
chr6:149718081 | T | TCGC | 3 | a0001c0001t0005 a0001c0001t0016 a0001c0001t0030 |
14 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-376_-374dupGCG | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15956 | chr6 | 149718081 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:149662474 | A | G | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2884-236T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662474 | |||||||
chr6:149662486 | C | G | 2 | a0001c0001t0004g0006 a0001c0001t0004g0208 |
3 | HG02602.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2884-248G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662486 | |||||||
chr6:149662672 | T | C | 1 | a0001c0002t0024g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2884-434A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662672 | |||||||
chr6:149662687 | C | T | 1 | a0001c0001t0004g0183 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2884-449G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662687 | |||||||
chr6:149662957 | C | T | 1 | a0001c0002t0003g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2884-719G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662957 | |||||||
chr6:149662966 | C | CA | 10 | a0001c0002t0002g0021 a0001c0002t0002g0053 a0001c0002t0002g0064 others(7): Show |
10 | HG01243.hp2 HG02040.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.2884-729dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662966 | |||||||
chr6:149662966 | CA | C | 138 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(135): Show |
140 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.2884-729delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662966 | |||||||
chr6:149662981 | A | G | 1 | a0001c0002t0003g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2884-743T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662981 | |||||||
chr6:149662982 | A | G | 131 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(128): Show |
133 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2884-744T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662982 | |||||||
chr6:149662983 | A | G | 1 | a0001c0010t0023g0009 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2884-745T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662983 | |||||||
chr6:149663057 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2884-819T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149663057 | |||||||
chr6:149663096 | G | A | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2884-858C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149663096 | |||||||
chr6:149663451 | G | T | 6 | a0001c0002t0003g0043 a0001c0002t0003g0044 a0001c0002t0003g0046 others(3): Show |
6 | HG03209.hp1 HG03225.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.2884-1213C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149663451 | |||||||
chr6:149663634 | T | C | 2 | a0001c0002t0002g0024 a0001c0002t0022g0101 |
2 | HG01106.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2884-1396A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149663634 | |||||||
chr6:149664079 | T | G | 181 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(178): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2884-1841A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664079 | |||||||
chr6:149664161 | CA | C | 133 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(130): Show |
135 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2884-1924delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664161 | |||||||
chr6:149664265 | A | C | 1 | a0001c0001t0001g0154 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2884-2027T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664265 | |||||||
chr6:149664340 | T | TGAG | 145 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(142): Show |
147 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2884-2103_2884-210 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664340 | |||||||
chr6:149664357 | T | A | 3 | a0001c0004t0013g0249 a0001c0004t0013g0250 a0001c0004t0013g0251 |
3 | HG02895.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2884-2119A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664357 | |||||||
chr6:149664708 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2884-2470C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664708 | |||||||
chr6:149664737 | A | T | 2 | a0001c0001t0001g0234 a0008c0009t0027g0233 |
2 | HG01175.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2884-2499T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664737 | |||||||
chr6:149664947 | T | G | 1 | a0001c0010t0023g0009 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2884-2709A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664947 | |||||||
chr6:149665035 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2884-2797G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149665035 | |||||||
chr6:149665191 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2884-2953C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149665191 | |||||||
chr6:149665371 | T | C | 1 | a0001c0002t0002g0051 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2884-3133A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149665371 | |||||||
chr6:149665490 | T | C | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2884-3252A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149665490 | |||||||
chr6:149665658 | T | A | 4 | a0001c0004t0012g0144 a0001c0004t0013g0249 a0001c0004t0013g0250 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2884-3420A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149665658 | |||||||
chr6:149666014 | C | G | 1 | a0001c0001t0004g0202 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2884-3776G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666014 | |||||||
chr6:149666015 | G | A | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2884-3777C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666015 | |||||||
chr6:149666015 | G | C | 1 | a0001c0001t0004g0202 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2884-3777C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666015 | |||||||
chr6:149666016 | C | T | 1 | a0001c0001t0004g0202 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2884-3778G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666016 | |||||||
chr6:149666018 | T | C | 1 | a0001c0001t0004g0202 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2884-3780A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666018 | |||||||
chr6:149666139 | C | CA | 55 | a0001c0001t0001g0129 a0001c0001t0001g0165 a0001c0001t0001g0222 others(52): Show |
57 | HG00099.hp1 HG01106.hp2 HG01175.hp1 others(54): Show |
intron_variant | MODIFIER | c.2884-3902dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666139 | |||||||
chr6:149666139 | C | CAA | 105 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0131 others(102): Show |
105 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.2884-3903_2884-390 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666139 | |||||||
chr6:149666139 | C | CAAA | 27 | a0001c0001t0001g0130 a0001c0001t0001g0147 a0001c0001t0001g0160 others(24): Show |
28 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.2884-3904_2884-390 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666139 | |||||||
chr6:149666139 | C | CAAAA | 5 | a0001c0001t0006g0007 a0001c0001t0006g0240 a0001c0001t0006g0242 others(2): Show |
6 | HG02109.hp1 HG02572.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2884-3905_2884-390 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666139 | |||||||
chr6:149666223 | A | G | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2884-3985T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666223 | |||||||
chr6:149666272 | A | C | 1 | a0001c0002t0003g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2884-4034T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666272 | |||||||
chr6:149666359 | TGTAATCC others(2): Show |
T | 7 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 others(4): Show |
7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2884-4130_2884-412 others(13): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666359 | |||||||
chr6:149666388 | C | T | 2 | a0001c0001t0007g0138 a0001c0001t0028g0139 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2884-4150G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666388 | |||||||
chr6:149666433 | C | T | 1 | a0001c0001t0005g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2884-4195G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666433 | |||||||
chr6:149666434 | G | A | 13 | a0001c0001t0001g0210 a0001c0001t0005g0252 a0001c0001t0005g0254 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2884-4196C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666434 | |||||||
chr6:149666461 | CA | C | 4 | a0001c0001t0005g0252 a0001c0001t0005g0261 a0001c0001t0005g0262 others(1): Show |
4 | HG02055.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2884-4224delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666461 | |||||||
chr6:149666803 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2884-4565C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666803 | |||||||
chr6:149666811 | G | A | 1 | a0001c0002t0003g0043 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2884-4573C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666811 | |||||||
chr6:149666892 | A | T | 2 | a0001c0004t0013g0250 a0001c0004t0013g0251 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2884-4654T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666892 | |||||||
chr6:149666900 | A | T | 2 | a0001c0004t0013g0250 a0001c0004t0013g0251 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2884-4662T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666900 | |||||||
chr6:149666940 | T | C | 12 | a0001c0002t0002g0003 a0001c0002t0002g0053 a0001c0002t0002g0055 others(9): Show |
13 | HG01358.hp1 HG02040.hp2 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.2884-4702A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666940 | |||||||
chr6:149666943 | C | CA | 11 | a0001c0001t0001g0160 a0001c0001t0001g0230 a0001c0001t0004g0202 others(8): Show |
11 | HG01496.hp2 HG02257.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.2884-4706dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666943 | |||||||
chr6:149666943 | CA | C | 6 | a0001c0001t0001g0223 a0001c0001t0007g0138 a0001c0001t0028g0139 others(3): Show |
6 | HG01069.hp1 HG02976.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2884-4706delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666943 | |||||||
chr6:149666974 | G | A | 1 | a0001c0001t0006g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2884-4736C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666974 | |||||||
chr6:149667200 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2884-4962G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667200 | |||||||
chr6:149667438 | C | CA | 25 | a0001c0001t0004g0202 a0001c0002t0002g0002 a0001c0002t0002g0021 others(22): Show |
26 | HG00099.hp1 HG01106.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.2884-5201dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667438 | |||||||
chr6:149667438 | CA | C | 24 | a0001c0001t0004g0175 a0001c0001t0004g0176 a0001c0001t0004g0205 others(21): Show |
25 | HG00140.hp1 HG01515.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.2884-5201delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667438 | |||||||
chr6:149667438 | CAA | C | 56 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0165 others(53): Show |
57 | HG00423.hp1 HG00423.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.2884-5202_2884-520 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667438 | |||||||
chr6:149667438 | CAAA | C | 59 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0130 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2884-5203_2884-520 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667438 | |||||||
chr6:149667438 | CAAAA | C | 9 | a0001c0001t0001g0129 a0001c0001t0001g0155 a0001c0001t0001g0189 others(6): Show |
9 | HG00741.hp2 HG01975.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2884-5204_2884-520 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667438 | |||||||
chr6:149667526 | C | A | 1 | a0001c0001t0004g0202 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2884-5288G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667526 | |||||||
chr6:149667527 | A | C | 1 | a0001c0001t0004g0202 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2884-5289T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667527 | |||||||
chr6:149667567 | A | G | 2 | a0001c0001t0006g0137 a0001c0001t0030g0265 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2884-5329T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667567 | |||||||
chr6:149667660 | C | T | 1 | a0001c0002t0003g0083 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2884-5422G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667660 | |||||||
chr6:149667702 | C | A | 1 | a0001c0002t0003g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2884-5464G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667702 | |||||||
chr6:149667929 | T | C | 141 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.2884-5691A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667929 | |||||||
chr6:149667952 | G | C | 1 | a0001c0001t0005g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2884-5714C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667952 | |||||||
chr6:149667964 | C | T | 10 | a0001c0002t0002g0024 a0001c0002t0002g0034 a0001c0002t0002g0084 others(7): Show |
10 | HG01106.hp1 HG01169.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.2884-5726G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667964 | |||||||
chr6:149668107 | C | T | 1 | a0001c0002t0014g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2884-5869G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668107 | |||||||
chr6:149668117 | ACATGTTG others(6149): Show |
A | 1 | a0001c0001t0001g0198 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2883+1987_2884-588 others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668117 | |||||||
chr6:149668443 | A | AT | 133 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(130): Show |
134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2884-6206dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668443 | |||||||
chr6:149668443 | A | ATT | 7 | a0001c0001t0001g0232 a0001c0001t0006g0007 a0001c0001t0006g0239 others(4): Show |
8 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2884-6207_2884-620 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668443 | |||||||
chr6:149668496 | T | C | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2884-6258A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668496 | |||||||
chr6:149668608 | AT | A | 139 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(136): Show |
141 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.2884-6371delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668608 | |||||||
chr6:149668635 | T | C | 141 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.2884-6397A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668635 | |||||||
chr6:149668666 | A | C | 2 | a0001c0002t0002g0060 a0001c0002t0018g0014 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2884-6428T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668666 | |||||||
chr6:149668870 | A | G | 2 | a0001c0001t0006g0137 a0001c0001t0030g0265 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2884-6632T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668870 | |||||||
chr6:149669173 | A | G | 144 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(141): Show |
146 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.2884-6935T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669173 | |||||||
chr6:149669224 | C | T | 1 | a0001c0001t0005g0257 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2884-6986G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669224 | |||||||
chr6:149669372 | A | G | 1 | a0001c0001t0007g0138 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2883+6888T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669372 | |||||||
chr6:149669447 | A | G | 144 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(141): Show |
146 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.2883+6813T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669447 | |||||||
chr6:149669482 | C | G | 1 | a0005c0016t0001g0200 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2883+6778G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669482 | |||||||
chr6:149669601 | T | C | 1 | a0001c0001t0004g0205 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2883+6659A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669601 | |||||||
chr6:149669715 | C | T | 1 | a0001c0001t0030g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2883+6545G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669715 | |||||||
chr6:149669744 | G | A | 1 | a0001c0002t0014g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2883+6516C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669744 | |||||||
chr6:149669820 | T | C | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2883+6440A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669820 | |||||||
chr6:149670008 | C | T | 2 | a0001c0001t0012g0168 a0001c0001t0012g0169 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2883+6252G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670008 | |||||||
chr6:149670171 | C | CA | 10 | a0001c0002t0002g0003 a0001c0002t0002g0012 a0001c0002t0002g0037 others(7): Show |
10 | HG01175.hp1 HG02071.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.2883+6088dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670171 | |||||||
chr6:149670171 | CA | C | 8 | a0001c0002t0002g0087 a0001c0002t0002g0113 a0001c0002t0002g0120 others(5): Show |
8 | HG00140.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2883+6088delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670171 | |||||||
chr6:149670182 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0209 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2883+6066_2883+607 others(16): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670182 | |||||||
chr6:149670188 | AAAAAAGA others(4): Show |
A | 28 | a0001c0002t0002g0049 a0001c0002t0003g0004 a0001c0002t0003g0023 others(25): Show |
29 | HG01192.hp2 HG02258.hp2 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.2883+6061_2883+607 others(15): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670188 | |||||||
chr6:149670188 | AAAAAAGA others(9): Show |
A | 1 | a0001c0002t0002g0116 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2883+6056_2883+607 others(20): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670188 | |||||||
chr6:149670189 | AAAAAG | A | 119 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(116): Show |
121 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.2883+6066_2883+607 others(9): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670189 | |||||||
chr6:149670189 | AAAAAGAA others(3): Show |
A | 4 | a0001c0001t0004g0148 a0001c0002t0003g0057 a0001c0002t0003g0103 others(1): Show |
4 | HG00099.hp1 HG01169.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.2883+6061_2883+607 others(14): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670189 | |||||||
chr6:149670190 | AAAAG | A | 12 | a0001c0001t0001g0181 a0001c0001t0001g0188 a0001c0001t0001g0194 others(9): Show |
12 | HG00738.hp2 HG03471.hp2 HG04184.hp2 others(9): Show |
intron_variant | MODIFIER | c.2883+6066_2883+606 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670190 | |||||||
chr6:149670267 | A | G | 2 | a0001c0001t0006g0137 a0001c0001t0030g0265 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2883+5993T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670267 | |||||||
chr6:149670284 | T | G | 6 | a0001c0001t0012g0168 a0001c0001t0012g0169 a0001c0004t0012g0144 others(3): Show |
6 | HG02615.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2883+5976A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670284 | |||||||
chr6:149670380 | G | T | 104 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(101): Show |
105 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.2883+5880C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670380 | |||||||
chr6:149670625 | T | C | 180 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(177): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.2883+5635A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670625 | |||||||
chr6:149670685 | C | T | 1 | a0001c0001t0004g0148 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2883+5575G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670685 | |||||||
chr6:149670880 | G | A | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2883+5380C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670880 | |||||||
chr6:149671122 | TTTTG | T | 140 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(137): Show |
142 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.2883+5134_2883+513 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671122 | |||||||
chr6:149671172 | A | G | 141 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.2883+5088T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671172 | |||||||
chr6:149671182 | G | A | 1 | a0001c0004t0013g0249 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2883+5078C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671182 | |||||||
chr6:149671240 | C | T | 141 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.2883+5020G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671240 | |||||||
chr6:149671294 | T | C | 3 | a0001c0002t0002g0049 a0003c0006t0002g0048 a0003c0006t0002g0058 |
3 | HG03209.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2883+4966A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671294 | |||||||
chr6:149671397 | G | A | 1 | a0001c0002t0003g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2883+4863C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671397 | |||||||
chr6:149671424 | G | A | 1 | a0001c0002t0003g0083 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2883+4836C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671424 | |||||||
chr6:149671508 | T | G | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2883+4752A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671508 | |||||||
chr6:149671572 | C | G | 144 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(141): Show |
146 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.2883+4688G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671572 | |||||||
chr6:149671588 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2883+4672A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671588 | |||||||
chr6:149671673 | T | A | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2883+4587A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671673 | |||||||
chr6:149671974 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0229 |
2 | HG03491.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2883+4286G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671974 | |||||||
chr6:149671999 | C | T | 129 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(126): Show |
131 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.2883+4261G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671999 | |||||||
chr6:149672171 | C | T | 1 | a0001c0002t0002g0003 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2883+4089G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149672171 | |||||||
chr6:149672458 | C | T | 2 | a0001c0001t0007g0138 a0001c0001t0028g0139 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2883+3802G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149672458 | |||||||
chr6:149672717 | G | A | 1 | a0001c0001t0005g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2883+3543C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149672717 | |||||||
chr6:149672905 | T | C | 141 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.2883+3355A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149672905 | |||||||
chr6:149673096 | C | CT | 14 | a0001c0002t0002g0003 a0001c0002t0002g0049 a0001c0002t0002g0053 others(11): Show |
15 | HG01358.hp1 HG02040.hp2 HG03209.hp2 others(12): Show |
intron_variant | MODIFIER | c.2883+3163dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673096 | |||||||
chr6:149673096 | CT | C | 7 | a0001c0002t0002g0016 a0001c0002t0002g0052 a0001c0002t0002g0104 others(4): Show |
7 | HG01069.hp2 HG01109.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.2883+3163delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673096 | |||||||
chr6:149673096 | CTT | C | 8 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(5): Show |
9 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2883+3162_2883+316 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673096 | |||||||
chr6:149673096 | CTTT | C | 127 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(124): Show |
128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.2883+3161_2883+316 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673096 | |||||||
chr6:149673678 | C | CT | 5 | a0001c0002t0002g0040 a0001c0002t0002g0078 a0001c0002t0009g0018 others(2): Show |
5 | HG00140.hp1 HG01358.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.2883+2581dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673678 | |||||||
chr6:149673678 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2883+2582G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673678 | |||||||
chr6:149673704 | C | T | 1 | a0001c0002t0002g0047 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2883+2556G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673704 | |||||||
chr6:149673831 | T | C | 7 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 others(4): Show |
7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2883+2429A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673831 | |||||||
chr6:149673970 | C | T | 3 | a0001c0002t0003g0083 a0004c0005t0003g0050 a0004c0005t0003g0059 |
3 | HG04115.hp1 NA18969.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2883+2290G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673970 | |||||||
chr6:149674221 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0229 a0001c0001t0012g0168 others(1): Show |
4 | HG02615.hp1 HG02630.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2883+2039G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674221 | |||||||
chr6:149674402 | A | C | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2883+1858T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674402 | |||||||
chr6:149674414 | C | T | 1 | a0001c0001t0004g0145 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2883+1846G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674414 | |||||||
chr6:149674433 | T | C | 1 | a0001c0001t0004g0176 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2883+1827A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674433 | |||||||
chr6:149674482 | C | G | 1 | a0001c0001t0007g0138 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2883+1778G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674482 | |||||||
chr6:149674639 | G | A | 105 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2883+1621C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674639 | |||||||
chr6:149674660 | C | G | 1 | a0001c0001t0004g0006 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2883+1600G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674660 | |||||||
chr6:149674695 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2883+1565A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674695 | |||||||
chr6:149674770 | C | CA | 13 | a0001c0001t0005g0252 a0001c0001t0005g0254 a0001c0001t0005g0255 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2883+1489dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674770 | |||||||
chr6:149675046 | G | A | 1 | a0001c0001t0004g0148 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2883+1214C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675046 | |||||||
chr6:149675109 | C | G | 1 | a0001c0002t0014g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2883+1151G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675109 | |||||||
chr6:149675111 | G | A | 1 | a0012c0011t0003g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2883+1149C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675111 | |||||||
chr6:149675215 | C | CA | 14 | a0001c0002t0002g0040 a0001c0002t0008g0001 a0001c0002t0008g0026 others(11): Show |
15 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2883+1044dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675215 | |||||||
chr6:149675215 | CA | C | 132 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(129): Show |
134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2883+1044delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675215 | |||||||
chr6:149675387 | G | A | 1 | a0001c0001t0005g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2883+873C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675387 | |||||||
chr6:149675588 | G | A | 142 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(139): Show |
144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2883+672C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675588 | |||||||
chr6:149675693 | A | T | 1 | a0001c0002t0003g0043 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2883+567T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675693 | |||||||
chr6:149675705 | T | C | 181 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(178): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2883+555A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675705 | |||||||
chr6:149675847 | G | A | 141 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.2883+413C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675847 | |||||||
chr6:149675853 | G | A | 3 | a0001c0001t0011g0184 a0001c0001t0011g0185 a0001c0001t0011g0227 |
3 | HG01433.hp1 HG02273.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2883+407C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675853 | |||||||
chr6:149675858 | A | G | 1 | a0001c0002t0003g0109 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2883+402T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675858 | |||||||
chr6:149675878 | T | C | 1 | a0001c0002t0003g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2883+382A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675878 | |||||||
chr6:149676001 | C | A | 6 | a0001c0002t0008g0001 a0001c0002t0008g0026 a0001c0002t0008g0027 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2883+259G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149676001 | |||||||
chr6:149676109 | C | T | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2883+151G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149676109 | |||||||
chr6:149676207 | C | A | 35 | a0001c0002t0002g0049 a0001c0002t0003g0004 a0001c0002t0003g0023 others(32): Show |
37 | HG00099.hp1 HG01192.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.2883+53G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149676207 | |||||||
chr6:149676521 | T | C | 181 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(178): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2776+34A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 6/7 | chr6 | 149676521 | |||||||
chr6:149676818 | G | A | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2594-81C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149676818 | |||||||
chr6:149676908 | T | C | 1 | a0012c0011t0003g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2594-171A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149676908 | |||||||
chr6:149677034 | C | A | 1 | a0001c0001t0004g0136 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2594-297G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677034 | |||||||
chr6:149677039 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2594-302A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677039 | |||||||
chr6:149677147 | A | AAAAC | 181 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(178): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2594-414_2594-411d others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677147 | |||||||
chr6:149677261 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2594-524C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677261 | |||||||
chr6:149677368 | C | A | 1 | a0009c0012t0003g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2594-631G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677368 | |||||||
chr6:149677378 | G | C | 1 | a0009c0012t0003g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2594-641C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677378 | |||||||
chr6:149677438 | T | C | 184 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(181): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2594-701A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677438 | |||||||
chr6:149677456 | T | TAGAAATG others(333): Show |
1 | a0001c0002t0008g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2594-720_2594-719i others(342): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677456 | |||||||
chr6:149677587 | A | G | 105 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2594-850T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677587 | |||||||
chr6:149677969 | G | A | 1 | a0001c0001t0004g0136 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2594-1232C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677969 | |||||||
chr6:149677977 | G | A | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2594-1240C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677977 | |||||||
chr6:149677993 | C | T | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2594-1256G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677993 | |||||||
chr6:149678018 | CA | C | 140 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(137): Show |
142 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.2594-1282delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678018 | |||||||
chr6:149678031 | A | C | 7 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 others(4): Show |
7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2594-1294T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678031 | |||||||
chr6:149678046 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2594-1309C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678046 | |||||||
chr6:149678086 | A | G | 145 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(142): Show |
147 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2594-1349T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678086 | |||||||
chr6:149678094 | G | A | 1 | a0001c0001t0004g0136 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2594-1357C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678094 | |||||||
chr6:149678162 | T | TA | 55 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(52): Show |
56 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2594-1426_2594-142 others(5): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678162 | |||||||
chr6:149678162 | TCC | T | 24 | a0001c0001t0028g0139 a0001c0002t0002g0049 a0001c0002t0003g0004 others(21): Show |
25 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.2594-1427_2594-142 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678162 | |||||||
chr6:149678162 | TCCA | T | 4 | a0001c0001t0006g0137 a0001c0002t0003g0117 a0001c0010t0023g0009 others(1): Show |
4 | HG02717.hp1 HG03540.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2594-1428_2594-142 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678162 | |||||||
chr6:149678162 | TCCAAAAA others(4): Show |
T | 1 | a0001c0002t0002g0036 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2594-1436_2594-142 others(15): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678162 | |||||||
chr6:149678162 | TCCAAAAA others(8): Show |
T | 6 | a0001c0002t0002g0032 a0001c0002t0002g0051 a0001c0002t0002g0065 others(3): Show |
6 | NA18955.hp2 NA18984.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.2594-1440_2594-142 others(19): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678162 | |||||||
chr6:149678163 | C | A | 171 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0150 others(168): Show |
176 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.2594-1426G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678163 | |||||||
chr6:149678164 | C | A | 55 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(52): Show |
56 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2594-1427G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678164 | |||||||
chr6:149678164 | C | CAA | 72 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0151 others(69): Show |
73 | HG00140.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.2594-1429_2594-142 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678164 | |||||||
chr6:149678164 | C | CAAA | 19 | a0001c0001t0001g0147 a0001c0001t0001g0159 a0001c0001t0001g0166 others(16): Show |
19 | HG00423.hp2 HG02027.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.2594-1430_2594-142 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678164 | |||||||
chr6:149678164 | CA | C | 22 | a0001c0001t0007g0138 a0001c0001t0030g0265 a0001c0002t0002g0060 others(19): Show |
23 | HG01515.hp1 HG01884.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.2594-1428delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678164 | |||||||
chr6:149678166 | A | C | 24 | a0001c0001t0028g0139 a0001c0002t0002g0049 a0001c0002t0003g0004 others(21): Show |
25 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.2594-1429T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678166 | |||||||
chr6:149678167 | A | C | 4 | a0001c0001t0006g0137 a0001c0002t0003g0117 a0001c0010t0023g0009 others(1): Show |
4 | HG02717.hp1 HG03540.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2594-1430T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678167 | |||||||
chr6:149678173 | A | C | 2 | a0004c0005t0003g0050 a0004c0005t0003g0059 |
2 | NA18969.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2594-1436T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678173 | |||||||
chr6:149678175 | A | C | 1 | a0001c0002t0002g0036 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2594-1438T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678175 | |||||||
chr6:149678179 | A | C | 6 | a0001c0002t0002g0032 a0001c0002t0002g0051 a0001c0002t0002g0065 others(3): Show |
6 | NA18955.hp2 NA18984.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.2594-1442T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678179 | |||||||
chr6:149678292 | C | A | 1 | a0012c0011t0003g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2594-1555G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678292 | |||||||
chr6:149678345 | A | AAAAC | 141 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.2593+1526_2593+152 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678345 | |||||||
chr6:149678426 | G | C | 2 | a0001c0001t0006g0137 a0001c0001t0030g0265 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2593+1449C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678426 | |||||||
chr6:149678467 | A | G | 2 | a0001c0001t0007g0138 a0001c0001t0028g0139 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2593+1408T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678467 | |||||||
chr6:149678615 | C | T | 1 | a0001c0001t0005g0254 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2593+1260G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678615 | |||||||
chr6:149678624 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2593+1251A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678624 | |||||||
chr6:149678651 | A | G | 14 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(11): Show |
14 | HG00423.hp2 HG01975.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.2593+1224T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678651 | |||||||
chr6:149678652 | T | C | 3 | a0001c0002t0002g0049 a0003c0006t0002g0048 a0003c0006t0002g0058 |
3 | HG03209.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2593+1223A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678652 | |||||||
chr6:149678831 | G | A | 5 | a0001c0002t0010g0005 a0001c0002t0010g0122 a0001c0002t0010g0123 others(2): Show |
6 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2593+1044C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678831 | |||||||
chr6:149679181 | T | C | 1 | a0001c0001t0004g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2593+694A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149679181 | |||||||
chr6:149679506 | G | C | 142 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(139): Show |
144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2593+369C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149679506 | |||||||
chr6:149679531 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2593+344C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149679531 | |||||||
chr6:149679549 | C | CA | 21 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0186 others(18): Show |
21 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.2593+325dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149679549 | |||||||
chr6:149679549 | CA | C | 16 | a0001c0001t0001g0132 a0001c0001t0001g0189 a0001c0001t0006g0007 others(13): Show |
18 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2593+325delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149679549 | |||||||
chr6:149679555 | A | C | 2 | a0003c0006t0002g0048 a0003c0006t0002g0058 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2593+320T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149679555 | |||||||
chr6:149680602 | C | A | 7 | a0001c0002t0002g0003 a0001c0002t0002g0067 a0001c0002t0002g0068 others(4): Show |
8 | NA18947.hp1 NA18952.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.2011-145G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680602 | |||||||
chr6:149680638 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2011-181C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680638 | |||||||
chr6:149680743 | G | GA | 111 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(108): Show |
112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.2011-287dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680743 | |||||||
chr6:149680743 | G | GAA | 24 | a0001c0001t0001g0158 a0001c0001t0001g0222 a0001c0001t0006g0007 others(21): Show |
25 | HG01884.hp1 HG02109.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.2011-288_2011-287d others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680743 | |||||||
chr6:149680743 | G | GGA | 12 | a0001c0001t0005g0252 a0001c0001t0005g0254 a0001c0001t0005g0255 others(9): Show |
12 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2011-287_2011-286i others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680743 | |||||||
chr6:149680786 | G | A | 1 | a0001c0001t0030g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2011-329C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680786 | |||||||
chr6:149680975 | T | C | 7 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 others(4): Show |
7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2011-518A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680975 | |||||||
chr6:149680990 | T | A | 1 | a0001c0001t0026g0182 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2011-533A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680990 | |||||||
chr6:149681766 | T | C | 142 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(139): Show |
144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2011-1309A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149681766 | |||||||
chr6:149681942 | G | A | 2 | a0001c0002t0014g0010 a0001c0010t0023g0009 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2010+1137C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149681942 | |||||||
chr6:149681975 | G | A | 2 | a0001c0001t0007g0138 a0001c0001t0028g0139 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2010+1104C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149681975 | |||||||
chr6:149682036 | C | T | 1 | a0001c0002t0002g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2010+1043G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682036 | |||||||
chr6:149682044 | G | A | 3 | a0001c0002t0002g0024 a0001c0002t0002g0102 a0001c0002t0022g0101 |
3 | HG01106.hp1 HG01169.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2010+1035C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682044 | |||||||
chr6:149682067 | G | C | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010+1012C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682067 | |||||||
chr6:149682090 | GAC | G | 105 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2010+987_2010+988d others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682090 | |||||||
chr6:149682110 | C | CA | 123 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(120): Show |
124 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.2010+968dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682110 | |||||||
chr6:149682120 | A | AT | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010+958_2010+959i others(3): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682120 | |||||||
chr6:149682184 | G | A | 2 | a0001c0001t0004g0245 a0001c0001t0004g0246 |
2 | NA18990.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2010+895C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682184 | |||||||
chr6:149682379 | G | C | 1 | a0001c0010t0023g0009 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2010+700C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682379 | |||||||
chr6:149682415 | C | CT | 6 | a0001c0001t0004g0237 a0001c0001t0005g0256 a0001c0002t0002g0097 others(3): Show |
6 | HG02257.hp1 HG02698.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.2010+663dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682415 | |||||||
chr6:149682419 | T | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0213 |
2 | HG02523.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2010+660A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682419 | |||||||
chr6:149682472 | C | T | 26 | a0001c0002t0003g0004 a0001c0002t0003g0023 a0001c0002t0003g0041 others(23): Show |
27 | HG00099.hp1 HG01192.hp2 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.2010+607G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682472 | |||||||
chr6:149682693 | C | A | 1 | a0001c0001t0026g0182 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2010+386G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682693 | |||||||
chr6:149682696 | G | A | 6 | a0001c0002t0008g0001 a0001c0002t0008g0026 a0001c0002t0008g0027 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010+383C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682696 | |||||||
chr6:149682706 | G | A | 1 | a0001c0001t0011g0185 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2010+373C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682706 | |||||||
chr6:149682759 | T | C | 2 | a0001c0001t0006g0137 a0001c0001t0030g0265 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2010+320A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682759 | |||||||
chr6:149682790 | C | T | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2010+289G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682790 | |||||||
chr6:149682891 | A | C | 142 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(139): Show |
144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2010+188T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682891 | |||||||
chr6:149684603 | A | G | 7 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 others(4): Show |
7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-11T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149684603 | |||||||
chr6:149684888 | A | G | 5 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 others(2): Show |
5 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-296T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149684888 | |||||||
chr6:149684938 | A | G | 2 | a0001c0002t0014g0010 a0001c0010t0023g0009 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.497-346T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149684938 | |||||||
chr6:149685131 | G | A | 1 | a0001c0002t0002g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.497-539C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149685131 | |||||||
chr6:149685192 | C | T | 4 | a0001c0004t0012g0144 a0001c0004t0013g0249 a0001c0004t0013g0250 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-600G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149685192 | |||||||
chr6:149685244 | A | T | 4 | a0001c0001t0005g0253 a0001c0002t0024g0124 a0001c0004t0013g0250 others(1): Show |
4 | HG02004.hp2 HG02258.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-652T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149685244 | |||||||
chr6:149685246 | T | A | 1 | a0001c0002t0014g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.497-654A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149685246 | |||||||
chr6:149685543 | G | A | 1 | a0001c0001t0006g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-951C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149685543 | |||||||
chr6:149685803 | CA | C | 139 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(136): Show |
141 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.497-1212delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149685803 | |||||||
chr6:149686020 | C | A | 2 | a0001c0001t0004g0207 a0001c0001t0029g0248 |
2 | NA18961.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.497-1428G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686020 | |||||||
chr6:149686274 | AAT | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-1684_497-1683d others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686274 | |||||||
chr6:149686463 | G | C | 1 | a0001c0002t0003g0112 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.497-1871C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686463 | |||||||
chr6:149686478 | G | A | 1 | a0001c0001t0006g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-1886C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686478 | |||||||
chr6:149686479 | C | T | 1 | a0001c0001t0006g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-1887G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686479 | |||||||
chr6:149686520 | T | A | 1 | a0001c0001t0001g0172 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.497-1928A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686520 | |||||||
chr6:149686926 | T | C | 1 | a0001c0002t0008g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.497-2334A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686926 | |||||||
chr6:149686941 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.497-2349A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686941 | |||||||
chr6:149687095 | A | AT | 137 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(134): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.497-2504dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687095 | |||||||
chr6:149687102 | T | A | 1 | a0001c0001t0028g0139 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.497-2510A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687102 | |||||||
chr6:149687145 | C | T | 1 | a0001c0002t0002g0062 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.497-2553G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687145 | |||||||
chr6:149687167 | C | T | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.497-2575G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687167 | |||||||
chr6:149687758 | G | A | 4 | a0002c0003t0007g0140 a0002c0003t0007g0141 a0002c0003t0007g0142 others(1): Show |
4 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-3166C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687758 | |||||||
chr6:149687873 | C | CT | 24 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(21): Show |
24 | HG01175.hp1 HG02055.hp1 HG02273.hp1 others(21): Show |
intron_variant | MODIFIER | c.497-3282dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687873 | |||||||
chr6:149687905 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.497-3313C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687905 | |||||||
chr6:149687975 | C | T | 6 | a0001c0001t0012g0168 a0001c0001t0012g0169 a0001c0004t0012g0144 others(3): Show |
6 | HG02615.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-3383G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687975 | |||||||
chr6:149688122 | G | C | 130 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(127): Show |
132 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.497-3530C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688122 | |||||||
chr6:149688390 | C | A | 7 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 others(4): Show |
7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-3798G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688390 | |||||||
chr6:149688410 | A | G | 1 | a0001c0002t0009g0061 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.497-3818T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688410 | |||||||
chr6:149688459 | C | T | 142 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(139): Show |
144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.497-3867G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688459 | |||||||
chr6:149688465 | C | A | 1 | a0010c0014t0002g0080 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.497-3873G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688465 | |||||||
chr6:149688507 | A | G | 2 | a0001c0001t0006g0137 a0001c0001t0030g0265 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.497-3915T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688507 | |||||||
chr6:149688551 | G | A | 11 | a0001c0001t0006g0137 a0001c0001t0007g0138 a0001c0001t0028g0139 others(8): Show |
11 | HG01884.hp1 HG02717.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-3959C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688551 | |||||||
chr6:149688603 | C | T | 1 | a0001c0002t0014g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.497-4011G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688603 | |||||||
chr6:149688609 | G | A | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.497-4017C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688609 | |||||||
chr6:149688609 | G | C | 11 | a0001c0001t0006g0137 a0001c0001t0007g0138 a0001c0001t0028g0139 others(8): Show |
11 | HG01884.hp1 HG02717.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-4017C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688609 | |||||||
chr6:149688650 | C | T | 1 | a0001c0001t0005g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-4058G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688650 | |||||||
chr6:149688893 | C | T | 1 | a0001c0001t0005g0254 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.497-4301G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688893 | |||||||
chr6:149689054 | G | C | 1 | a0001c0001t0007g0138 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.497-4462C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689054 | |||||||
chr6:149689358 | C | A | 1 | a0001c0001t0028g0139 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.497-4766G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689358 | |||||||
chr6:149689418 | C | CA | 117 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(114): Show |
118 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.497-4827dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689418 | |||||||
chr6:149689418 | C | CAA | 10 | a0001c0001t0001g0164 a0001c0001t0001g0211 a0001c0001t0001g0226 others(7): Show |
11 | HG00738.hp2 HG00741.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-4828_497-4827d others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689418 | |||||||
chr6:149689533 | C | T | 12 | a0001c0001t0005g0252 a0001c0001t0005g0254 a0001c0001t0005g0255 others(9): Show |
12 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.497-4941G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689533 | |||||||
chr6:149689596 | C | T | 1 | a0001c0001t0006g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-5004G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689596 | |||||||
chr6:149689653 | C | T | 1 | a0001c0001t0026g0182 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.497-5061G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689653 | |||||||
chr6:149689781 | T | A | 1 | a0001c0001t0006g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-5189A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689781 | |||||||
chr6:149689971 | T | TA | 39 | a0001c0001t0004g0145 a0001c0002t0002g0002 a0001c0002t0002g0003 others(36): Show |
42 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.496+5102dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689971 | |||||||
chr6:149689985 | T | A | 1 | a0001c0002t0003g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.496+5089A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689985 | |||||||
chr6:149690150 | C | T | 180 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(177): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.496+4924G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690150 | |||||||
chr6:149690186 | T | C | 9 | a0001c0001t0005g0252 a0001c0001t0005g0255 a0001c0001t0005g0256 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.496+4888A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690186 | |||||||
chr6:149690213 | C | CT | 5 | a0001c0002t0002g0047 a0001c0002t0003g0081 a0001c0002t0003g0103 others(2): Show |
5 | HG01109.hp1 HG02080.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+4860dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690213 | |||||||
chr6:149690213 | CT | C | 132 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(129): Show |
134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.496+4860delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690213 | |||||||
chr6:149690266 | T | G | 1 | a0001c0001t0001g0244 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.496+4808A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690266 | |||||||
chr6:149690449 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.496+4625C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690449 | |||||||
chr6:149690506 | C | A | 1 | a0001c0002t0003g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.496+4568G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690506 | |||||||
chr6:149690551 | C | CT | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+4522dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690551 | |||||||
chr6:149690581 | C | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+4493G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690581 | |||||||
chr6:149690605 | G | T | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.496+4469C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690605 | |||||||
chr6:149691226 | T | C | 142 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(139): Show |
144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.496+3848A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691226 | |||||||
chr6:149691286 | C | T | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+3788G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691286 | |||||||
chr6:149691668 | A | G | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+3406T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691668 | |||||||
chr6:149691770 | C | T | 1 | a0001c0010t0023g0009 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.496+3304G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691770 | |||||||
chr6:149691832 | T | C | 5 | a0001c0002t0003g0004 a0001c0002t0003g0042 a0001c0002t0003g0117 others(2): Show |
6 | HG01192.hp2 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+3242A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691832 | |||||||
chr6:149691880 | A | G | 1 | a0001c0002t0002g0036 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.496+3194T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691880 | |||||||
chr6:149691923 | C | T | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.496+3151G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691923 | |||||||
chr6:149692155 | C | T | 1 | a0001c0002t0014g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.496+2919G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692155 | |||||||
chr6:149692163 | T | G | 6 | a0001c0001t0001g0163 a0001c0001t0001g0187 a0001c0001t0001g0191 others(3): Show |
6 | HG00099.hp2 HG00738.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+2911A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692163 | |||||||
chr6:149692208 | G | C | 1 | a0001c0001t0005g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.496+2866C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692208 | |||||||
chr6:149692442 | T | C | 2 | a0001c0001t0012g0168 a0001c0001t0012g0169 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.496+2632A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692442 | |||||||
chr6:149692677 | C | CT | 12 | a0001c0001t0005g0252 a0001c0001t0005g0253 a0001c0001t0005g0254 others(9): Show |
12 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.496+2396dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692677 | |||||||
chr6:149692677 | CT | C | 5 | a0001c0001t0004g0148 a0001c0001t0026g0182 a0001c0002t0002g0017 others(2): Show |
5 | HG01169.hp1 HG01975.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+2396delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692677 | |||||||
chr6:149692705 | G | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0162 |
2 | HG00741.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.496+2369C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692705 | |||||||
chr6:149692821 | C | T | 130 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(127): Show |
132 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.496+2253G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692821 | |||||||
chr6:149692824 | G | A | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.496+2250C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692824 | |||||||
chr6:149693003 | G | A | 2 | a0001c0001t0006g0137 a0001c0002t0002g0102 |
2 | HG02717.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.496+2071C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693003 | |||||||
chr6:149693022 | C | T | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.496+2052G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693022 | |||||||
chr6:149693254 | G | A | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+1820C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693254 | |||||||
chr6:149693334 | A | G | 180 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(177): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.496+1740T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693334 | |||||||
chr6:149693339 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.496+1735G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693339 | |||||||
chr6:149693567 | G | A | 3 | a0001c0001t0001g0229 a0001c0001t0007g0138 a0001c0002t0014g0010 |
3 | HG02976.hp2 HG03471.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.496+1507C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693567 | |||||||
chr6:149693591 | C | T | 4 | a0001c0002t0002g0085 a0001c0002t0002g0086 a0001c0002t0015g0035 others(1): Show |
4 | NA18945.hp2 NA19009.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+1483G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693591 | |||||||
chr6:149693611 | A | AAAAC | 6 | a0001c0002t0002g0021 a0001c0002t0002g0116 a0001c0002t0003g0023 others(3): Show |
6 | HG03490.hp2 HG04115.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+1459_496+1462d others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693611 | |||||||
chr6:149693611 | AAAAC | A | 10 | a0001c0001t0007g0138 a0001c0001t0028g0139 a0001c0002t0002g0012 others(7): Show |
10 | HG00642.hp1 HG01109.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+1459_496+1462d others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693611 | |||||||
chr6:149693611 | AAAACAAA others(1): Show |
A | 132 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(129): Show |
134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.496+1455_496+1462d others(10): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693611 | |||||||
chr6:149693611 | AAAACAAA others(5): Show |
A | 1 | a0001c0001t0004g0231 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.496+1451_496+1462d others(14): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693611 | |||||||
chr6:149693743 | C | T | 1 | a0001c0002t0002g0021 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.496+1331G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693743 | |||||||
chr6:149693835 | A | G | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.496+1239T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693835 | |||||||
chr6:149693894 | A | T | 105 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.496+1180T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693894 | |||||||
chr6:149693903 | A | T | 1 | a0001c0001t0007g0138 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.496+1171T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693903 | |||||||
chr6:149693947 | C | T | 6 | a0001c0002t0003g0004 a0001c0002t0003g0041 a0001c0002t0003g0042 others(3): Show |
7 | HG01192.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+1127G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693947 | |||||||
chr6:149694051 | C | T | 2 | a0001c0001t0006g0137 a0001c0001t0030g0265 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.496+1023G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149694051 | |||||||
chr6:149694122 | G | A | 180 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(177): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.496+952C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149694122 | |||||||
chr6:149694162 | G | A | 1 | a0002c0003t0007g0141 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496+912C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149694162 | |||||||
chr6:149694304 | T | C | 1 | a0001c0002t0002g0120 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.496+770A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149694304 | |||||||
chr6:149694601 | C | T | 1 | a0001c0001t0005g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.496+473G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149694601 | |||||||
chr6:149694765 | T | C | 2 | a0001c0001t0016g0258 a0001c0001t0016g0259 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.496+309A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149694765 | |||||||
chr6:149695345 | T | A | 2 | a0001c0001t0007g0138 a0001c0001t0028g0139 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.349-124A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695345 | |||||||
chr6:149695366 | A | T | 1 | a0001c0002t0014g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.349-145T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695366 | |||||||
chr6:149695392 | T | G | 7 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 others(4): Show |
7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-171A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695392 | |||||||
chr6:149695393 | C | T | 7 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 others(4): Show |
7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-172G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695393 | |||||||
chr6:149695440 | G | A | 141 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.349-219C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695440 | |||||||
chr6:149695491 | T | C | 1 | a0010c0014t0002g0080 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.349-270A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695491 | |||||||
chr6:149695554 | G | A | 2 | a0001c0002t0014g0010 a0001c0010t0023g0009 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.349-333C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695554 | |||||||
chr6:149695676 | G | GA | 15 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0151 others(12): Show |
16 | HG00140.hp2 HG00741.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.349-456dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695676 | |||||||
chr6:149695676 | GA | G | 139 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.349-456delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695676 | |||||||
chr6:149695781 | C | T | 1 | a0001c0001t0017g0008 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.349-560G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695781 | |||||||
chr6:149695804 | A | C | 2 | a0001c0001t0007g0138 a0001c0001t0028g0139 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.349-583T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695804 | |||||||
chr6:149695812 | T | C | 2 | a0001c0002t0014g0010 a0001c0010t0023g0009 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.349-591A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695812 | |||||||
chr6:149695949 | A | G | 1 | a0001c0001t0005g0254 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.349-728T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695949 | |||||||
chr6:149695958 | G | A | 1 | a0001c0004t0012g0144 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.349-737C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695958 | |||||||
chr6:149695967 | C | T | 36 | a0001c0002t0002g0049 a0001c0002t0003g0004 a0001c0002t0003g0023 others(33): Show |
38 | HG00099.hp1 HG01192.hp2 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.349-746G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695967 | |||||||
chr6:149695968 | G | A | 1 | a0001c0002t0002g0104 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.349-747C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695968 | |||||||
chr6:149696152 | C | T | 2 | a0001c0002t0002g0093 a0001c0002t0002g0094 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.349-931G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696152 | |||||||
chr6:149696167 | A | T | 12 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(9): Show |
13 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.349-946T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696167 | |||||||
chr6:149696203 | A | C | 1 | a0001c0010t0023g0009 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.349-982T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696203 | |||||||
chr6:149696280 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.349-1059A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696280 | |||||||
chr6:149696335 | G | A | 2 | a0001c0002t0014g0010 a0001c0010t0023g0009 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.349-1114C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696335 | |||||||
chr6:149696414 | T | C | 30 | a0001c0002t0002g0049 a0001c0002t0003g0004 a0001c0002t0003g0023 others(27): Show |
31 | HG00099.hp1 HG01192.hp2 HG02080.hp1 others(28): Show |
intron_variant | MODIFIER | c.349-1193A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696414 | |||||||
chr6:149696554 | C | T | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349-1333G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696554 | |||||||
chr6:149696555 | G | A | 1 | a0001c0001t0030g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.349-1334C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696555 | |||||||
chr6:149696559 | T | TA | 97 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0130 others(94): Show |
99 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(96): Show |
intron_variant | MODIFIER | c.349-1339dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696559 | |||||||
chr6:149696559 | T | TAA | 41 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(38): Show |
41 | HG00642.hp2 HG01074.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.349-1340_349-1339d others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696559 | |||||||
chr6:149696559 | T | TAAA | 6 | a0001c0001t0001g0159 a0001c0001t0001g0216 a0001c0001t0001g0217 others(3): Show |
6 | HG00423.hp2 HG00438.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-1341_349-1339d others(5): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696559 | |||||||
chr6:149696559 | TA | T | 8 | a0001c0001t0004g0153 a0001c0002t0002g0015 a0001c0002t0002g0032 others(5): Show |
8 | HG00099.hp1 HG00423.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-1339delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696559 | |||||||
chr6:149696560 | A | T | 6 | a0001c0002t0008g0001 a0001c0002t0008g0026 a0001c0002t0008g0027 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-1339T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696560 | |||||||
chr6:149696642 | C | T | 145 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(142): Show |
147 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.349-1421G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696642 | |||||||
chr6:149696840 | T | C | 1 | a0001c0002t0002g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.349-1619A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696840 | |||||||
chr6:149696911 | T | C | 1 | a0001c0002t0002g0021 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.349-1690A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696911 | |||||||
chr6:149696964 | C | A | 1 | a0012c0011t0003g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.349-1743G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696964 | |||||||
chr6:149696988 | C | T | 6 | a0001c0001t0012g0168 a0001c0001t0012g0169 a0001c0004t0012g0144 others(3): Show |
6 | HG02615.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-1767G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696988 | |||||||
chr6:149697352 | G | T | 7 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 others(4): Show |
7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-2131C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697352 | |||||||
chr6:149697452 | T | A | 1 | a0001c0002t0002g0049 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.349-2231A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697452 | |||||||
chr6:149697477 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.349-2256C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697477 | |||||||
chr6:149697489 | G | A | 1 | a0001c0002t0008g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.349-2268C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697489 | |||||||
chr6:149697507 | A | G | 1 | a0001c0002t0014g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.349-2286T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697507 | |||||||
chr6:149697952 | T | C | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-2731A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697952 | |||||||
chr6:149697960 | G | C | 1 | a0001c0001t0001g0222 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.349-2739C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697960 | |||||||
chr6:149698036 | G | A | 1 | a0001c0001t0006g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.349-2815C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698036 | |||||||
chr6:149698239 | CTT | C | 143 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(140): Show |
145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.349-3020_349-3019d others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698239 | |||||||
chr6:149698254 | T | C | 6 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0151 others(3): Show |
6 | HG00140.hp2 HG00741.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-3033A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698254 | |||||||
chr6:149698552 | C | CT | 5 | a0001c0001t0001g0232 a0001c0001t0004g0203 a0001c0002t0002g0084 others(2): Show |
5 | HG01361.hp1 HG02135.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+3226dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698552 | |||||||
chr6:149698589 | C | T | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.348+3190G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698589 | |||||||
chr6:149698637 | G | A | 1 | a0001c0001t0006g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.348+3142C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698637 | |||||||
chr6:149698770 | C | T | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.348+3009G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698770 | |||||||
chr6:149698841 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.348+2938C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698841 | |||||||
chr6:149698972 | A | G | 1 | a0001c0001t0006g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.348+2807T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698972 | |||||||
chr6:149699020 | G | T | 1 | a0001c0002t0002g0045 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.348+2759C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699020 | |||||||
chr6:149699058 | CA | C | 144 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(141): Show |
146 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.348+2720delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699058 | |||||||
chr6:149699199 | C | T | 1 | a0001c0001t0005g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.348+2580G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699199 | |||||||
chr6:149699277 | A | G | 2 | a0001c0002t0014g0010 a0001c0010t0023g0009 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.348+2502T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699277 | |||||||
chr6:149699308 | GTCTGGGA others(13): Show |
G | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.348+2451_348+2470d others(22): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699308 | |||||||
chr6:149699365 | C | A | 1 | a0001c0002t0003g0081 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.348+2414G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699365 | |||||||
chr6:149699365 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.348+2414G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699365 | |||||||
chr6:149699380 | G | A | 1 | a0001c0010t0023g0009 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.348+2399C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699380 | |||||||
chr6:149699417 | G | T | 141 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.348+2362C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699417 | |||||||
chr6:149699453 | A | C | 1 | a0001c0002t0002g0116 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.348+2326T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699453 | |||||||
chr6:149699482 | A | T | 8 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(5): Show |
9 | HG01109.hp1 HG02109.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+2297T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699482 | |||||||
chr6:149699483 | A | T | 1 | a0001c0002t0014g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.348+2296T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699483 | |||||||
chr6:149699567 | T | C | 1 | a0001c0002t0014g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.348+2212A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699567 | |||||||
chr6:149699730 | G | T | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348+2049C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699730 | |||||||
chr6:149699936 | T | A | 2 | a0001c0001t0012g0168 a0001c0001t0012g0169 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.348+1843A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699936 | |||||||
chr6:149700161 | C | T | 145 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(142): Show |
147 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.348+1618G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700161 | |||||||
chr6:149700168 | T | C | 1 | a0001c0002t0020g0071 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.348+1611A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700168 | |||||||
chr6:149700285 | C | T | 6 | a0001c0001t0001g0188 a0001c0001t0001g0199 a0001c0001t0001g0201 others(3): Show |
6 | HG02523.hp1 NA18967.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+1494G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700285 | |||||||
chr6:149700355 | C | A | 7 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 others(4): Show |
7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.348+1424G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700355 | |||||||
chr6:149700363 | C | T | 2 | a0001c0002t0003g0023 a0009c0012t0003g0056 |
2 | HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.348+1416G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700363 | |||||||
chr6:149700451 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.348+1328A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700451 | |||||||
chr6:149700602 | G | A | 6 | a0001c0002t0008g0001 a0001c0002t0008g0026 a0001c0002t0008g0027 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+1177C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700602 | |||||||
chr6:149700602 | G | C | 1 | a0001c0002t0003g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.348+1177C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700602 | |||||||
chr6:149700733 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.348+1046A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700733 | |||||||
chr6:149700741 | AT | A | 142 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(139): Show |
144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.348+1037delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700741 | |||||||
chr6:149700852 | C | T | 9 | a0001c0001t0005g0252 a0001c0001t0005g0255 a0001c0001t0005g0256 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+927G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700852 | |||||||
chr6:149700885 | G | A | 9 | a0001c0001t0007g0138 a0001c0001t0028g0139 a0002c0003t0007g0133 others(6): Show |
9 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+894C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700885 | |||||||
chr6:149701086 | C | T | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348+693G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149701086 | |||||||
chr6:149701097 | A | G | 11 | a0001c0001t0006g0137 a0001c0001t0007g0138 a0001c0001t0028g0139 others(8): Show |
11 | HG01884.hp1 HG02717.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.348+682T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149701097 | |||||||
chr6:149701291 | C | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+488G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149701291 | |||||||
chr6:149701451 | C | A | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348+328G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149701451 | |||||||
chr6:149701752 | C | T | 3 | a0001c0004t0013g0249 a0001c0004t0013g0250 a0001c0004t0013g0251 |
3 | HG02895.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.348+27G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149701752 | |||||||
chr6:149702291 | A | C | 1 | a0001c0001t0001g0172 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-140-25T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702291 | |||||||
chr6:149702367 | T | G | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140-101A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702367 | |||||||
chr6:149702397 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0004g0247 |
2 | HG01243.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-140-131G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702397 | |||||||
chr6:149702480 | A | AT | 3 | a0001c0004t0012g0144 a0001c0004t0013g0250 a0001c0004t0013g0251 |
3 | HG02895.hp1 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-140-215dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702480 | |||||||
chr6:149702483 | TA | T | 9 | a0001c0001t0001g0181 a0001c0001t0001g0187 a0001c0001t0001g0196 others(6): Show |
9 | HG00099.hp2 HG01069.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-140-218delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702483 | |||||||
chr6:149702497 | AAGTT | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-140-235_-140-232d others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702497 | |||||||
chr6:149702517 | C | T | 130 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(127): Show |
132 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-140-251G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702517 | |||||||
chr6:149702577 | T | G | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-140-311A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702577 | |||||||
chr6:149702732 | T | C | 182 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(179): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.-140-466A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702732 | |||||||
chr6:149702799 | A | G | 1 | a0001c0002t0002g0060 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-140-533T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702799 | |||||||
chr6:149702964 | T | C | 145 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(142): Show |
147 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.-140-698A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702964 | |||||||
chr6:149702975 | T | C | 1 | a0002c0003t0007g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-140-709A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702975 | |||||||
chr6:149703130 | C | A | 1 | a0001c0002t0003g0081 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-140-864G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149703130 | |||||||
chr6:149703149 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-140-883A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149703149 | |||||||
chr6:149703358 | T | C | 7 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 others(4): Show |
7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-140-1092A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149703358 | |||||||
chr6:149703730 | T | C | 2 | a0001c0002t0014g0010 a0001c0010t0023g0009 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-1464A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149703730 | |||||||
chr6:149703986 | C | T | 105 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-140-1720G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149703986 | |||||||
chr6:149704096 | C | A | 1 | a0001c0002t0002g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-140-1830G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704096 | |||||||
chr6:149704097 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-140-1831C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704097 | |||||||
chr6:149704158 | C | T | 1 | a0001c0001t0004g0208 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-140-1892G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704158 | |||||||
chr6:149704159 | G | A | 2 | a0001c0002t0014g0010 a0001c0010t0023g0009 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-1893C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704159 | |||||||
chr6:149704229 | C | G | 29 | a0001c0002t0002g0049 a0001c0002t0003g0004 a0001c0002t0003g0023 others(26): Show |
30 | HG00099.hp1 HG01192.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.-140-1963G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704229 | |||||||
chr6:149704231 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-140-1965C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704231 | |||||||
chr6:149704483 | T | G | 2 | a0001c0001t0030g0265 a0005c0016t0001g0200 |
2 | HG00642.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-140-2217A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704483 | |||||||
chr6:149704493 | G | GT | 102 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(99): Show |
103 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-140-2228dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704493 | |||||||
chr6:149704493 | G | T | 4 | a0001c0001t0001g0212 a0001c0001t0004g0148 a0001c0001t0004g0245 others(1): Show |
4 | HG01169.hp1 HG03831.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140-2227C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704493 | |||||||
chr6:149704510 | A | G | 2 | a0004c0005t0003g0050 a0004c0005t0003g0059 |
2 | NA18969.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-140-2244T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704510 | |||||||
chr6:149704824 | T | G | 1 | a0001c0002t0002g0036 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-140-2558A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704824 | |||||||
chr6:149704860 | A | T | 29 | a0001c0002t0002g0049 a0001c0002t0003g0004 a0001c0002t0003g0023 others(26): Show |
30 | HG00099.hp1 HG01192.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.-140-2594T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704860 | |||||||
chr6:149704880 | TTAATTA | T | 2 | a0001c0002t0002g0020 a0001c0002t0002g0022 |
2 | HG01106.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-140-2620_-140-261 others(10): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704880 | |||||||
chr6:149704883 | A | C | 3 | a0001c0001t0001g0127 a0001c0002t0014g0010 a0001c0010t0023g0009 |
3 | HG02280.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-2617T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704883 | |||||||
chr6:149704884 | T | A | 3 | a0001c0001t0001g0127 a0001c0002t0014g0010 a0001c0010t0023g0009 |
3 | HG02280.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-2618A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704884 | |||||||
chr6:149704884 | TTA | T | 4 | a0001c0002t0009g0018 a0001c0002t0009g0019 a0001c0004t0013g0250 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-140-2620_-140-261 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704884 | |||||||
chr6:149704885 | T | C | 3 | a0001c0001t0001g0127 a0001c0002t0014g0010 a0001c0010t0023g0009 |
3 | HG02280.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-2619A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704885 | |||||||
chr6:149704885 | TATACACA others(7): Show |
T | 1 | a0001c0004t0012g0144 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-140-2633_-140-262 others(18): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704885 | |||||||
chr6:149704887 | T | C | 4 | a0001c0001t0001g0127 a0001c0002t0014g0010 a0001c0004t0013g0249 others(1): Show |
4 | HG02280.hp2 HG03471.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140-2621A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | |||||||
chr6:149704887 | T | TAC | 14 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0209 others(11): Show |
14 | HG01074.hp2 HG01175.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-140-2623_-140-262 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | |||||||
chr6:149704887 | T | TACAC | 12 | a0001c0001t0001g0181 a0001c0001t0001g0211 a0001c0001t0001g0236 others(9): Show |
12 | HG00438.hp1 HG00741.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.-140-2625_-140-262 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | |||||||
chr6:149704887 | T | TACACAC | 34 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(31): Show |
34 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.-140-2627_-140-262 others(10): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | |||||||
chr6:149704887 | T | TACACACA others(1): Show |
25 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0149 others(22): Show |
25 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.-140-2629_-140-262 others(12): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | |||||||
chr6:149704887 | T | TACACACA others(3): Show |
4 | a0001c0001t0001g0163 a0001c0001t0001g0201 a0001c0001t0005g0253 others(1): Show |
4 | HG01361.hp2 HG02258.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140-2631_-140-262 others(14): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | |||||||
chr6:149704887 | T | TACACACA others(5): Show |
11 | a0001c0001t0001g0164 a0001c0001t0001g0220 a0001c0001t0001g0224 others(8): Show |
11 | HG00738.hp2 HG01358.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-140-2633_-140-262 others(16): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | |||||||
chr6:149704887 | T | TACACACA others(9): Show |
1 | a0001c0001t0005g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-140-2637_-140-262 others(20): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | |||||||
chr6:149704887 | TAC | T | 87 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0004g0136 others(84): Show |
90 | HG00423.hp1 HG00642.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.-140-2623_-140-262 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | |||||||
chr6:149704887 | TACAC | T | 9 | a0001c0001t0004g0145 a0001c0002t0002g0037 a0001c0002t0002g0060 others(6): Show |
9 | HG00140.hp1 HG02572.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-140-2625_-140-262 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | |||||||
chr6:149704887 | TACACAC | T | 35 | a0001c0001t0004g0202 a0001c0001t0004g0238 a0001c0001t0006g0137 others(32): Show |
37 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.-140-2627_-140-262 others(10): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | |||||||
chr6:149704889 | C | T | 2 | a0001c0002t0002g0020 a0001c0002t0002g0022 |
2 | HG01106.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-140-2623G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704889 | |||||||
chr6:149704933 | G | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-140-2667C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704933 | |||||||
chr6:149704954 | G | A | 2 | a0001c0002t0014g0010 a0001c0010t0023g0009 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-2688C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704954 | |||||||
chr6:149705060 | T | C | 105 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-140-2794A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149705060 | |||||||
chr6:149705201 | C | T | 2 | a0001c0001t0004g0221 a0006c0013t0004g0171 |
2 | HG01074.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-140-2935G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149705201 | |||||||
chr6:149705292 | T | C | 1 | a0001c0001t0030g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-140-3026A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149705292 | |||||||
chr6:149705343 | C | G | 1 | a0001c0001t0030g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-140-3077G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149705343 | |||||||
chr6:149705598 | G | A | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140-3332C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149705598 | |||||||
chr6:149705739 | T | C | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140-3473A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149705739 | |||||||
chr6:149706059 | T | C | 2 | a0001c0002t0014g0010 a0001c0010t0023g0009 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-3793A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706059 | |||||||
chr6:149706064 | T | C | 1 | a0001c0002t0003g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-140-3798A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706064 | |||||||
chr6:149706068 | A | G | 4 | a0001c0004t0012g0144 a0001c0004t0013g0249 a0001c0004t0013g0250 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140-3802T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706068 | |||||||
chr6:149706075 | C | T | 1 | a0001c0002t0003g0109 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-140-3809G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706075 | |||||||
chr6:149706124 | G | A | 1 | a0001c0001t0004g0231 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-140-3858C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706124 | |||||||
chr6:149706144 | T | C | 7 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 others(4): Show |
7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-140-3878A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706144 | |||||||
chr6:149706164 | C | A | 1 | a0001c0001t0004g0152 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-140-3898G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706164 | |||||||
chr6:149706183 | C | CA | 6 | a0001c0002t0002g0017 a0001c0002t0002g0093 a0001c0002t0002g0094 others(3): Show |
6 | HG01175.hp1 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.-140-3918dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | |||||||
chr6:149706183 | C | CAA | 6 | a0001c0002t0002g0012 a0001c0002t0002g0097 a0001c0002t0002g0098 others(3): Show |
6 | HG01433.hp2 HG02698.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-140-3919_-140-391 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | |||||||
chr6:149706183 | C | CAAAAAAA others(6): Show |
1 | a0001c0002t0002g0100 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-140-3930_-140-391 others(17): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | |||||||
chr6:149706183 | CA | C | 22 | a0001c0002t0002g0022 a0001c0002t0002g0025 a0001c0002t0002g0077 others(19): Show |
24 | HG01106.hp2 HG01192.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.-140-3918delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | |||||||
chr6:149706183 | CAA | C | 31 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0060 others(28): Show |
32 | HG00099.hp1 HG00140.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-140-3919_-140-391 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | |||||||
chr6:149706183 | CAAA | C | 16 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0032 others(13): Show |
18 | HG01069.hp2 HG01071.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.-140-3920_-140-391 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | |||||||
chr6:149706183 | CAAAAAAA others(2): Show |
C | 12 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0222 others(9): Show |
12 | HG02004.hp1 HG02559.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-140-3926_-140-391 others(13): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | |||||||
chr6:149706183 | CAAAAAAA others(3): Show |
C | 46 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0147 others(43): Show |
47 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-140-3927_-140-391 others(14): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | |||||||
chr6:149706183 | CAAAAAAA others(4): Show |
C | 70 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(67): Show |
71 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-140-3928_-140-391 others(15): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | |||||||
chr6:149706183 | CAAAAAAA others(5): Show |
C | 13 | a0001c0001t0005g0252 a0001c0001t0005g0254 a0001c0001t0005g0255 others(10): Show |
13 | HG02615.hp1 HG02895.hp1 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.-140-3929_-140-391 others(16): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | |||||||
chr6:149706183 | CAAAAAAA others(6): Show |
C | 1 | a0001c0004t0013g0250 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-140-3930_-140-391 others(17): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | |||||||
chr6:149706183 | CAAAAAAA others(14): Show |
C | 2 | a0001c0002t0003g0043 a0001c0002t0003g0044 |
2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-140-3938_-140-391 others(25): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | |||||||
chr6:149706183 | CAAAAAAA others(15): Show |
C | 1 | a0001c0002t0002g0047 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-140-3939_-140-391 others(26): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | |||||||
chr6:149706196 | A | G | 1 | a0001c0001t0004g0237 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-140-3930T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706196 | |||||||
chr6:149706336 | G | A | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140-4070C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706336 | |||||||
chr6:149706349 | C | T | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140-4083G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706349 | |||||||
chr6:149707011 | C | CT | 123 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(120): Show |
124 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.-140-4746dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707011 | |||||||
chr6:149707011 | C | CTT | 12 | a0001c0001t0004g0245 a0001c0001t0005g0254 a0001c0001t0030g0265 others(9): Show |
13 | HG01192.hp2 HG01884.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-140-4747_-140-474 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707011 | |||||||
chr6:149707011 | CT | C | 5 | a0001c0002t0002g0024 a0001c0002t0002g0102 a0001c0002t0002g0120 others(2): Show |
5 | HG01106.hp1 HG01169.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-140-4746delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707011 | |||||||
chr6:149707158 | G | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-140-4892C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707158 | |||||||
chr6:149707283 | G | A | 1 | a0001c0001t0028g0139 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-140-5017C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707283 | |||||||
chr6:149707383 | G | A | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-140-5117C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707383 | |||||||
chr6:149707441 | G | A | 1 | a0001c0002t0003g0103 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-140-5175C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707441 | |||||||
chr6:149707534 | T | C | 7 | a0001c0002t0002g0036 a0001c0002t0002g0037 a0001c0002t0002g0038 others(4): Show |
7 | HG02027.hp2 HG02132.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.-140-5268A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707534 | |||||||
chr6:149707787 | G | A | 1 | a0001c0002t0003g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-140-5521C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707787 | |||||||
chr6:149707880 | A | C | 1 | a0001c0001t0004g0170 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-140-5614T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707880 | |||||||
chr6:149708151 | C | G | 2 | a0001c0001t0012g0168 a0001c0001t0012g0169 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-140-5885G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708151 | |||||||
chr6:149708172 | G | T | 12 | a0001c0001t0005g0252 a0001c0001t0005g0254 a0001c0001t0005g0255 others(9): Show |
12 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-140-5906C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708172 | |||||||
chr6:149708414 | CA | C | 148 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(145): Show |
150 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.-140-6149delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708414 | |||||||
chr6:149708616 | A | T | 1 | a0001c0002t0002g0104 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-140-6350T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708616 | |||||||
chr6:149708775 | A | T | 1 | a0001c0001t0030g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-140-6509T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708775 | |||||||
chr6:149708870 | C | T | 6 | a0001c0002t0008g0001 a0001c0002t0008g0026 a0001c0002t0008g0027 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-140-6604G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708870 | |||||||
chr6:149708922 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG00140.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-140-6656T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708922 | |||||||
chr6:149709055 | T | C | 3 | a0001c0004t0013g0249 a0001c0004t0013g0250 a0001c0004t0013g0251 |
3 | HG02895.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-140-6789A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709055 | |||||||
chr6:149709180 | G | A | 1 | a0001c0001t0005g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-140-6914C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709180 | |||||||
chr6:149709212 | C | T | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-140-6946G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709212 | |||||||
chr6:149709251 | A | C | 1 | a0001c0001t0001g0236 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-140-6985T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709251 | |||||||
chr6:149709463 | C | T | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140-7197G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709463 | |||||||
chr6:149709493 | G | A | 1 | a0001c0010t0023g0009 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-140-7227C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709493 | |||||||
chr6:149709668 | C | CT | 99 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(96): Show |
100 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.-140-7403dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709668 | |||||||
chr6:149709668 | C | CTT | 24 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0149 others(21): Show |
24 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.-140-7404_-140-740 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709668 | |||||||
chr6:149709668 | CT | C | 15 | a0001c0002t0002g0104 a0001c0002t0002g0107 a0001c0002t0002g0108 others(12): Show |
15 | HG01516.hp1 HG02132.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140-7403delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709668 | |||||||
chr6:149709668 | CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0019g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-140-7415_-140-740 others(17): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709668 | |||||||
chr6:149709678 | T | C | 7 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 others(4): Show |
7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-140-7412A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709678 | |||||||
chr6:149709937 | G | A | 1 | a0001c0002t0002g0116 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-140-7671C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709937 | |||||||
chr6:149710043 | C | T | 1 | a0001c0001t0005g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-140-7777G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149710043 | |||||||
chr6:149710254 | T | C | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+7595A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149710254 | |||||||
chr6:149710593 | C | T | 4 | a0001c0004t0012g0144 a0001c0004t0013g0249 a0001c0004t0013g0250 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-141+7256G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149710593 | |||||||
chr6:149710647 | T | C | 1 | a0001c0002t0003g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-141+7202A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149710647 | |||||||
chr6:149710710 | G | A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0008c0009t0027g0233 |
3 | HG01074.hp2 HG01175.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-141+7139C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149710710 | |||||||
chr6:149710906 | T | G | 12 | a0001c0001t0005g0252 a0001c0001t0005g0254 a0001c0001t0005g0255 others(9): Show |
12 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-141+6943A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149710906 | |||||||
chr6:149711033 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-141+6816C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711033 | |||||||
chr6:149711111 | T | C | 142 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(139): Show |
144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.-141+6738A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711111 | |||||||
chr6:149711115 | C | T | 1 | a0001c0001t0004g0145 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-141+6734G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711115 | |||||||
chr6:149711178 | T | C | 2 | a0001c0001t0004g0237 a0001c0001t0004g0238 |
2 | NA18977.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-141+6671A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711178 | |||||||
chr6:149711253 | A | T | 11 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(8): Show |
12 | HG01169.hp2 HG02109.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-141+6596T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711253 | |||||||
chr6:149711254 | AT | A | 8 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(5): Show |
9 | HG00738.hp1 HG01106.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-141+6594delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711254 | |||||||
chr6:149711294 | C | T | 1 | a0001c0002t0003g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-141+6555G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711294 | |||||||
chr6:149711715 | G | T | 3 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 |
3 | HG01106.hp2 HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-141+6134C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711715 | |||||||
chr6:149711843 | G | C | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+6006C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711843 | |||||||
chr6:149711888 | G | A | 1 | a0001c0001t0006g0243 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-141+5961C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711888 | |||||||
chr6:149711896 | T | C | 145 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(142): Show |
147 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.-141+5953A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711896 | |||||||
chr6:149712153 | A | C | 2 | a0001c0002t0009g0018 a0001c0002t0009g0019 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-141+5696T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149712153 | |||||||
chr6:149712221 | T | C | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+5628A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149712221 | |||||||
chr6:149712355 | C | T | 130 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(127): Show |
132 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-141+5494G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149712355 | |||||||
chr6:149712484 | A | G | 3 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0017 |
3 | NA18951.hp1 NA19060.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-141+5365T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149712484 | |||||||
chr6:149712647 | G | A | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+5202C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149712647 | |||||||
chr6:149712922 | G | A | 1 | a0001c0001t0030g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-141+4927C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149712922 | |||||||
chr6:149713003 | T | A | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+4846A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713003 | |||||||
chr6:149713267 | C | T | 1 | a0001c0004t0012g0144 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-141+4582G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713267 | |||||||
chr6:149713363 | C | T | 1 | a0001c0002t0018g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-141+4486G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713363 | |||||||
chr6:149713364 | G | A | 1 | a0001c0002t0014g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-141+4485C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713364 | |||||||
chr6:149713406 | T | C | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-141+4443A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713406 | |||||||
chr6:149713455 | C | T | 1 | a0001c0001t0005g0252 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-141+4394G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713455 | |||||||
chr6:149713496 | A | G | 3 | a0001c0001t0004g0136 a0001c0001t0004g0245 a0001c0001t0004g0246 |
3 | NA18990.hp1 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-141+4353T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713496 | |||||||
chr6:149713572 | A | T | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+4277T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713572 | |||||||
chr6:149713574 | G | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0239 a0001c0001t0006g0240 others(3): Show |
7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-141+4275C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713574 | |||||||
chr6:149713752 | C | T | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+4097G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713752 | |||||||
chr6:149713919 | C | T | 131 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(128): Show |
133 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-141+3930G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713919 | |||||||
chr6:149713954 | G | A | 1 | a0001c0010t0023g0009 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-141+3895C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713954 | |||||||
chr6:149714174 | G | A | 2 | a0001c0002t0014g0010 a0001c0010t0023g0009 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-141+3675C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149714174 | |||||||
chr6:149714623 | A | C | 1 | a0013c0015t0021g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+3226T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149714623 | |||||||
chr6:149714640 | T | G | 143 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(140): Show |
145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.-141+3209A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149714640 | |||||||
chr6:149714836 | T | C | 4 | a0001c0002t0003g0004 a0001c0002t0003g0117 a0001c0002t0003g0118 others(1): Show |
5 | HG01192.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-141+3013A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149714836 | |||||||
chr6:149715046 | T | A | 1 | a0001c0001t0001g0244 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-141+2803A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149715046 | |||||||
chr6:149715109 | C | T | 4 | a0001c0004t0012g0144 a0001c0004t0013g0249 a0001c0004t0013g0250 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-141+2740G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149715109 | |||||||
chr6:149715279 | G | C | 3 | a0001c0001t0004g0136 a0001c0001t0004g0245 a0001c0001t0004g0246 |
3 | NA18990.hp1 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-141+2570C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149715279 | |||||||
chr6:149715309 | T | C | 1 | a0001c0001t0004g0247 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-141+2540A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149715309 | |||||||
chr6:149715895 | T | C | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-141+1954A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149715895 | |||||||
chr6:149716268 | T | C | 132 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(129): Show |
134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-141+1581A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149716268 | |||||||
chr6:149716299 | A | G | 1 | a0001c0001t0006g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-141+1550T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149716299 | |||||||
chr6:149716436 | A | G | 146 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(143): Show |
148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.-141+1413T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149716436 | |||||||
chr6:149716438 | C | T | 1 | a0001c0002t0002g0013 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-141+1411G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149716438 | |||||||
chr6:149716807 | A | G | 146 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(143): Show |
148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.-141+1042T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149716807 | |||||||
chr6:149716971 | T | A | 1 | a0001c0002t0002g0120 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-141+878A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149716971 | |||||||
chr6:149717070 | T | G | 1 | a0007c0007t0014g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-141+779A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149717070 | |||||||
chr6:149717096 | A | G | 1 | a0001c0010t0023g0009 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-141+753T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149717096 | |||||||
chr6:149717234 | C | T | 1 | a0001c0001t0004g0136 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-141+615G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149717234 | |||||||
chr6:149717667 | C | T | 3 | a0002c0003t0007g0133 a0002c0003t0007g0134 a0002c0003t0007g0135 |
3 | HG03579.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-141+182G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149717667 | |||||||
chr6:149717707 | C | G | 6 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-141+142G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149717707 |