Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7462 |
| ensemblid | ENSG00000086730.17 |
| hgncid | 12749 |
| symbol | LAT2 |
| name | linker for activation of T cells family member 2 |
| refseq_nuc | NM_032464.3 |
| refseq_prot | NP_115853.2 |
| ensembl_nuc | ENST00000460943.6 |
| ensembl_prot | ENSP00000420494.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 74210006 |
| end | 74229834 |
| strand | + |
| ver | v1.2 |
| region | chr7:74210006-74229834 |
| region5000 | chr7:74205006-74234834 |
| regionname0 | LAT2_chr7_74210006_74229834 |
| regionname5000 | LAT2_chr7_74205006_74234834 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 243 | 336 | 86 | 70 | 122 | 14 | 42 | 81 | LAT2_chr7_74205006_74234834 | LAT2 | MSSGT others(238): Show |
chr7 | 74205006 | 74234834 |
| a0002 | 0/0 | 243 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | MSSGT others(238): Show |
chr7 | 74205006 | 74234834 |
| a0003 | 0/0 | 243 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | MSSGT others(238): Show |
chr7 | 74205006 | 74234834 |
| a0004 | 0/0 | 243 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | MSSGT others(238): Show |
chr7 | 74205006 | 74234834 |
| a0005 | 0/0 | 243 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | MSSGT others(238): Show |
chr7 | 74205006 | 74234834 |
| a0006 | 0/0 | 243 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | MSSGT others(238): Show |
chr7 | 74205006 | 74234834 |
| a0007 | 0/0 | 243 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | MSSGT others(238): Show |
chr7 | 74205006 | 74234834 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 729 | 325 | 82 | 69 | 116 | 14 | 42 | LAT2_chr7_74205006_74234834 | LAT2 | ATGAG others(724): Show |
chr7 | 74205006 | 74234834 | ||
| a0001c0002 | 0/0 | 729 | 5 | 4 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | ATGAG others(724): Show |
chr7 | 74205006 | 74234834 | ||
| a0001c0003 | 0/0 | 729 | 4 | 0 | 0 | 4 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | ATGAG others(724): Show |
chr7 | 74205006 | 74234834 | ||
| a0001c0005 | 0/0 | 729 | 2 | 0 | 0 | 2 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | ATGAG others(724): Show |
chr7 | 74205006 | 74234834 | ||
| a0002c0004 | 0/0 | 729 | 3 | 0 | 3 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | ATGAG others(724): Show |
chr7 | 74205006 | 74234834 | ||
| a0003c0008 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | ATGAG others(724): Show |
chr7 | 74205006 | 74234834 | ||
| a0004c0009 | 0/0 | 729 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | ATGAG others(724): Show |
chr7 | 74205006 | 74234834 | ||
| a0005c0007 | 0/0 | 729 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | ATGAG others(724): Show |
chr7 | 74205006 | 74234834 | ||
| a0006c0006 | 0/0 | 729 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | ATGAG others(724): Show |
chr7 | 74205006 | 74234834 | ||
| a0007c0010 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | ATGAG others(724): Show |
chr7 | 74205006 | 74234834 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1942 | 307 | 70 | 67 | 114 | 14 | 40 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0001c0001t0002 | 0/0 | 1942 | 9 | 9 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0001c0001t0003 | 0/0 | 1942 | 2 | 1 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0001c0001t0004 | 0/0 | 1942 | 2 | 0 | 0 | 2 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0001c0001t0005 | 0/0 | 1942 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0001c0001t0006 | 0/0 | 1942 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0001c0001t0007 | 0/0 | 1942 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0001c0001t0008 | 0/0 | 1942 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0001c0001t0009 | 0/0 | 1942 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0001c0002t0001 | 0/0 | 1942 | 5 | 4 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0001c0003t0001 | 0/0 | 1942 | 4 | 0 | 0 | 4 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0001c0005t0001 | 0/0 | 1942 | 2 | 0 | 0 | 2 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0002c0004t0001 | 0/0 | 1942 | 3 | 0 | 3 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0003c0008t0001 | 0/0 | 1942 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0004c0009t0001 | 0/0 | 1942 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0005c0007t0001 | 0/0 | 1942 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0006c0006t0001 | 0/0 | 1942 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| a0007c0010t0001 | 0/0 | 1942 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | AGTGT others(1937): Show |
chr7 | 74205006 | 74234834 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0018 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0306 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0007g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0001t0009g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0005t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0001c0005t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0002c0004t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0002c0004t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0003c0008t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0004c0009t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0005c0007t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0006c0006t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| a0007c0010t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | GBR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | GBR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | FIN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | FIN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | CHS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00558 | hp2 | a0003 | c0008 | t0001 | g0077 | EAS | CHS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00597 | hp2 | a0001 | c0003 | t0001 | g0054 | EAS | CHS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00738 | hp1 | a0002 | c0004 | t0001 | g0005 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01255 | hp1 | a0002 | c0004 | t0001 | g0147 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0203 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01358 | hp1 | a0002 | c0004 | t0001 | g0005 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | IBS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01891 | hp1 | a0004 | c0009 | t0001 | g0036 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CDX | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02258 | hp1 | a0005 | c0007 | t0001 | g0200 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02300 | hp2 | a0006 | c0006 | t0001 | g0187 | AMR | PEL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0152 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03017 | hp1 | a0001 | c0001 | t0009 | g0057 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | MSL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | MSL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | BEB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | BEB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0312 | SAS | STU | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG04199 | hp2 | a0001 | c0001 | t0007 | g0093 | SAS | STU | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | STU | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | YRI | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0067 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18947 | hp2 | a0001 | c0005 | t0001 | g0130 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18960 | hp2 | a0001 | c0005 | t0001 | g0016 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19010 | hp2 | a0007 | c0010 | t0001 | g0138 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | LWK | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | YRI | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ASW | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | TSI | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | GIH | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | GIH | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | MSL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | USA | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | USA | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | USA | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | USA | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0306 | REF | REF | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0018 | REF | REF | LAT2_chr7_74205006_74234834 | LAT2 | chr7 | 74205006 | 74234834 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:74216054 | C | T | 1 | a0007 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.79C>T | p.Arg27Cys | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 3/14 | 380/1942 | 79/732 | 27/243 | chr7 | 74216054 | |||
| chr7:74216825 | G | T | 1 | a0004 | 1 | HG01891.hp1 | missense_variant&splice_region_variant | MODERATE | c.95G>T | p.Gly32Val | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/14 | 396/1942 | 95/732 | 32/243 | chr7 | 74216825 | |||
| chr7:74216847 | C | G | 1 | a0002 | 3 | HG00738.hp1 HG01255.hp1 HG01358.hp1 |
missense_variant | MODERATE | c.117C>G | p.Ile39Met | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/14 | 418/1942 | 117/732 | 39/243 | chr7 | 74216847 | |||
| chr7:74220733 | A | G | 1 | a0003 | 1 | HG00558.hp2 | missense_variant&splice_region_variant | MODERATE | c.331A>G | p.Ile111Val | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/14 | 632/1942 | 331/732 | 111/243 | chr7 | 74220733 | |||
| chr7:74223744 | G | A | 1 | a0006 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.409G>A | p.Glu137Lys | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 11/14 | 710/1942 | 409/732 | 137/243 | chr7 | 74223744 | |||
| chr7:74224686 | G | A | 1 | a0005 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.676G>A | p.Glu226Lys | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/14 | 977/1942 | 676/732 | 226/243 | chr7 | 74224686 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:74216014 | G | A | 1 | a0001c0003 | 4 | HG00558.hp1 HG00597.hp2 HG02015.hp1 others(1): Show |
synonymous_variant | LOW | c.39G>A | p.Ala13Ala | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 3/14 | 340/1942 | 39/732 | 13/243 | chr7 | 74216014 | |||
| chr7:74221688 | A | G | 1 | a0001c0002 | 5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
synonymous_variant | LOW | c.384A>G | p.Pro128Pro | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/14 | 685/1942 | 384/732 | 128/243 | chr7 | 74221688 | |||
| chr7:74224121 | G | A | 1 | a0001c0005 | 2 | NA18947.hp2 NA18960.hp2 |
synonymous_variant | LOW | c.552G>A | p.Pro184Pro | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 12/14 | 853/1942 | 552/732 | 184/243 | chr7 | 74224121 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:74210072 | G | A | 1 | a0001c0001t0002 | 9 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-235G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/14 | 5904 | chr7 | 74210072 | ||||||
| chr7:74210076 | C | G | 1 | a0001c0001t0004 | 2 | HG02040.hp2 NA18998.hp1 |
5_prime_UTR_variant | MODIFIER | c.-231C>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/14 | 5900 | chr7 | 74210076 | ||||||
| chr7:74229021 | C | T | 1 | a0001c0001t0009 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 14/14 | 4279 | chr7 | 74229021 | ||||||
| chr7:74229070 | G | A | 1 | a0001c0001t0005 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*145G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 14/14 | 4328 | chr7 | 74229070 | ||||||
| chr7:74229135 | G | A | 1 | a0001c0001t0003 | 2 | HG01074.hp2 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*210G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 14/14 | 4393 | chr7 | 74229135 | ||||||
| chr7:74229144 | C | T | 1 | a0001c0001t0002 | 9 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*219C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 14/14 | 4402 | chr7 | 74229144 | ||||||
| chr7:74229194 | C | G | 1 | a0001c0001t0008 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*269C>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 14/14 | 4452 | chr7 | 74229194 | ||||||
| chr7:74229212 | C | T | 1 | a0001c0001t0007 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*287C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 14/14 | 4470 | chr7 | 74229212 | ||||||
| chr7:74229506 | A | G | 1 | a0001c0001t0006 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*581A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 14/14 | 4764 | chr7 | 74229506 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:74210197 | C | T | 2 | a0001c0001t0001g0315 a0001c0001t0001g0316 |
2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-219+109C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74210197 | |||||||
| chr7:74210278 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-219+190T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74210278 | |||||||
| chr7:74210285 | C | T | 93 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(90): Show |
97 | HG00741.hp2 HG01069.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.-219+197C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74210285 | |||||||
| chr7:74210358 | GTA | G | 12 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(9): Show |
12 | HG01074.hp2 HG01081.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-219+271_-219+272d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74210358 | |||||||
| chr7:74210361 | A | G | 12 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(9): Show |
12 | HG01074.hp2 HG01081.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-219+273A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74210361 | |||||||
| chr7:74210402 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-219+314C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74210402 | |||||||
| chr7:74210460 | C | T | 1 | a0001c0001t0003g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-219+372C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74210460 | |||||||
| chr7:74210513 | C | T | 1 | a0001c0001t0001g0313 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-219+425C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74210513 | |||||||
| chr7:74210551 | A | G | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
11 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-219+463A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74210551 | |||||||
| chr7:74210594 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-219+506C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74210594 | |||||||
| chr7:74210798 | T | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(34): Show |
38 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.-219+710T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74210798 | |||||||
| chr7:74210808 | T | A | 8 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | HG01074.hp2 HG01243.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-219+720T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74210808 | |||||||
| chr7:74210951 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG02083.hp1 HG02135.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-219+863G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74210951 | |||||||
| chr7:74211012 | GC | G | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-219+928delC | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74211012 | ||||||
| chr7:74211120 | G | GCCCCCAC others(3): Show |
1 | a0001c0001t0001g0224 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-219+1035_-219+104 others(14): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74211120 | ||||||
| chr7:74211132 | C | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
6 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-219+1044C>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74211132 | |||||||
| chr7:74211138 | G | T | 1 | a0001c0001t0003g0069 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-219+1050G>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74211138 | |||||||
| chr7:74211243 | G | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(37): Show |
41 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.-219+1155G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74211243 | |||||||
| chr7:74211326 | G | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-219+1238G>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74211326 | |||||||
| chr7:74211337 | C | T | 1 | a0001c0001t0003g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-219+1249C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74211337 | |||||||
| chr7:74211526 | T | C | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
11 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-219+1438T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74211526 | |||||||
| chr7:74211531 | C | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-219+1443C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74211531 | |||||||
| chr7:74211614 | C | G | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-219+1526C>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74211614 | |||||||
| chr7:74211642 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-219+1554A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74211642 | |||||||
| chr7:74211848 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-219+1760T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74211848 | |||||||
| chr7:74211849 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-219+1761C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74211849 | |||||||
| chr7:74211932 | CTGTT | C | 10 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(7): Show |
10 | HG00558.hp2 HG00673.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.-219+1849_-219+185 others(8): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74211932 | ||||||
| chr7:74212035 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-219+1947C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74212035 | |||||||
| chr7:74212182 | C | T | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-219+2094C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74212182 | |||||||
| chr7:74212222 | C | T | 1 | a0001c0002t0001g0029 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-219+2134C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74212222 | |||||||
| chr7:74212380 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-219+2292C>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74212380 | |||||||
| chr7:74212495 | T | A | 1 | a0001c0001t0001g0088 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-218-2327T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74212495 | |||||||
| chr7:74212653 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-218-2169C>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74212653 | |||||||
| chr7:74212930 | G | T | 1 | a0001c0001t0001g0222 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-218-1892G>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74212930 | |||||||
| chr7:74212978 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-218-1844C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74212978 | |||||||
| chr7:74213262 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-218-1560C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213262 | |||||||
| chr7:74213291 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-218-1531G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213291 | |||||||
| chr7:74213293 | A | T | 1 | a0001c0001t0001g0090 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-218-1529A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213293 | |||||||
| chr7:74213296 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-218-1526C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213296 | |||||||
| chr7:74213420 | C | CT | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01943.hp1 HG02056.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-1402_-218-140 others(5): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213420 | |||||||
| chr7:74213421 | A | AT | 46 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0195 others(43): Show |
47 | HG00597.hp1 HG00621.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.-218-1380dupT | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74213421 | ||||||
| chr7:74213421 | A | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(28): Show |
32 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.-218-1401A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213421 | |||||||
| chr7:74213421 | AT | A | 13 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0073 others(10): Show |
13 | HG01081.hp2 HG01515.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-218-1380delT | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74213421 | ||||||
| chr7:74213453 | C | T | 4 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(1): Show |
4 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-1369C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213453 | |||||||
| chr7:74213573 | T | A | 1 | a0001c0001t0001g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-218-1249T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213573 | |||||||
| chr7:74213573 | T | C | 1 | a0002c0004t0001g0005 | 2 | HG00738.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-218-1249T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213573 | |||||||
| chr7:74213630 | G | A | 1 | a0001c0001t0007g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-218-1192G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213630 | |||||||
| chr7:74213632 | T | C | 1 | a0001c0001t0007g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-218-1190T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213632 | |||||||
| chr7:74213637 | C | A | 1 | a0001c0001t0007g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-218-1185C>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213637 | |||||||
| chr7:74213639 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-1183A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213639 | |||||||
| chr7:74213702 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-218-1120C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213702 | |||||||
| chr7:74213703 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-218-1119G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213703 | |||||||
| chr7:74213707 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-218-1115G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213707 | |||||||
| chr7:74213715 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-218-1107G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213715 | |||||||
| chr7:74213781 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0094 |
3 | HG02630.hp1 HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-218-1041G>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74213781 | |||||||
| chr7:74214031 | CATATATA others(5): Show |
C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0068 |
2 | HG02165.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-218-782_-218-771d others(14): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214031 | ||||||
| chr7:74214040 | G | GTA | 8 | a0001c0001t0001g0025 a0001c0001t0001g0142 a0001c0001t0001g0205 others(5): Show |
8 | HG00140.hp2 HG02630.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-218-766_-218-765d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214040 | ||||||
| chr7:74214040 | G | GTATA | 8 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-218-768_-218-765d others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214040 | ||||||
| chr7:74214045 | T | TATATATA others(21): Show |
1 | a0001c0001t0001g0096 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-218-738_-218-711d others(30): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214045 | ||||||
| chr7:74214045 | TATATATA others(21): Show |
T | 1 | a0001c0001t0001g0090 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-218-738_-218-711d others(30): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214045 | ||||||
| chr7:74214063 | A | T | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-759A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214063 | |||||||
| chr7:74214065 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-218-757T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214065 | |||||||
| chr7:74214071 | T | A | 3 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 |
3 | HG02630.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-218-751T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214071 | |||||||
| chr7:74214075 | T | A | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-747T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214075 | |||||||
| chr7:74214082 | A | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0311 |
2 | HG02683.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-218-740A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214082 | |||||||
| chr7:74214091 | A | T | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-731A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214091 | |||||||
| chr7:74214091 | AATATATA others(19): Show |
A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0064 |
3 | HG01943.hp1 NA18977.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-218-697_-218-672d others(28): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214091 | ||||||
| chr7:74214099 | T | A | 1 | a0001c0002t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-218-723T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214099 | |||||||
| chr7:74214101 | A | AAT | 12 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(9): Show |
12 | HG01074.hp2 HG01081.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-218-712_-218-711d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214101 | ||||||
| chr7:74214101 | A | AATATATA others(23): Show |
1 | a0001c0001t0001g0226 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-218-711_-218-710i others(32): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214101 | ||||||
| chr7:74214113 | AAAATATA others(5): Show |
A | 1 | a0001c0001t0001g0291 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-218-696_-218-685d others(14): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214113 | ||||||
| chr7:74214117 | T | A | 4 | a0001c0001t0001g0097 a0001c0001t0001g0226 a0001c0001t0001g0230 others(1): Show |
4 | HG01074.hp2 HG01928.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.-218-705T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214117 | |||||||
| chr7:74214117 | T | TATATATA others(17): Show |
7 | a0001c0001t0001g0131 a0001c0001t0001g0150 a0001c0001t0001g0199 others(4): Show |
7 | HG01109.hp2 HG02145.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218-671_-218-648d others(26): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214117 | ||||||
| chr7:74214117 | TATATATA others(17): Show |
T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0223 |
3 | HG01070.hp1 HG01071.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-218-671_-218-648d others(26): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214117 | ||||||
| chr7:74214125 | T | A | 1 | a0001c0002t0001g0029 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-218-697T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214125 | |||||||
| chr7:74214125 | T | TAAATATA others(7): Show |
2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG01496.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.-218-685_-218-672d others(16): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214125 | ||||||
| chr7:74214127 | A | AAT | 10 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(7): Show |
10 | HG01081.hp2 HG01243.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-218-686_-218-685d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214127 | ||||||
| chr7:74214139 | AAAATATA others(3): Show |
A | 28 | a0001c0001t0001g0228 a0001c0001t0001g0270 a0001c0001t0001g0271 others(25): Show |
28 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.-218-671_-218-662d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214139 | ||||||
| chr7:74214139 | AAAATATA others(17): Show |
A | 60 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(57): Show |
63 | HG00673.hp2 HG01106.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.-218-671_-218-648d others(26): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214139 | ||||||
| chr7:74214141 | A | AAT | 14 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(11): Show |
14 | HG01243.hp2 HG01361.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.-218-673_-218-672d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214141 | ||||||
| chr7:74214149 | TAAATATA others(7): Show |
T | 1 | a0001c0001t0001g0025 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-218-647_-218-634d others(16): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214149 | ||||||
| chr7:74214150 | A | AAATATAT others(19): Show |
1 | a0001c0001t0001g0234 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-218-669_-218-644d others(28): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214150 | ||||||
| chr7:74214150 | A | ATAAATAT others(37): Show |
1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-672_-218-671i others(46): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214150 | |||||||
| chr7:74214150 | A | ATG | 14 | a0001c0001t0001g0182 a0001c0001t0001g0225 a0001c0001t0001g0233 others(11): Show |
14 | HG01069.hp1 HG01081.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.-218-672_-218-671i others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214150 | |||||||
| chr7:74214150 | A | ATGAAAAT others(19): Show |
1 | a0001c0001t0001g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-218-672_-218-671i others(28): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214150 | |||||||
| chr7:74214151 | A | AAAAT | 3 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 |
3 | HG02630.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-218-670_-218-669i others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214151 | ||||||
| chr7:74214151 | A | AAAATATA others(207): Show |
1 | a0001c0002t0001g0029 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-218-670_-218-669i others(216): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214151 | ||||||
| chr7:74214151 | A | T | 1 | a0004c0009t0001g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-218-671A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214151 | |||||||
| chr7:74214153 | T | A | 16 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0225 others(13): Show |
16 | HG01069.hp1 HG01081.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.-218-669T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214153 | |||||||
| chr7:74214153 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0238 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-218-660_-218-649d others(14): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214153 | ||||||
| chr7:74214161 | TGA | T | 14 | a0001c0001t0001g0182 a0001c0001t0001g0225 a0001c0001t0001g0233 others(11): Show |
14 | HG01069.hp1 HG01081.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.-218-660_-218-659d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214161 | |||||||
| chr7:74214163 | A | AAAATATA others(3): Show |
25 | a0001c0001t0001g0228 a0001c0001t0001g0271 a0001c0001t0001g0272 others(22): Show |
25 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.-218-657_-218-648d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214163 | ||||||
| chr7:74214165 | A | AATATATA others(7): Show |
3 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 |
3 | HG02630.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-218-648_-218-647i others(16): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214165 | ||||||
| chr7:74214165 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-218-647_-218-646i others(16): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214165 | ||||||
| chr7:74214165 | A | AATATATA others(19): Show |
1 | a0004c0009t0001g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-218-649_-218-648i others(28): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214165 | ||||||
| chr7:74214165 | AAT | A | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0291 |
3 | HG01346.hp2 HG01496.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.-218-648_-218-647d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214165 | ||||||
| chr7:74214167 | T | TATATATG others(3): Show |
1 | a0001c0001t0001g0287 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-218-649_-218-648i others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214167 | ||||||
| chr7:74214173 | TATGAAAA others(33): Show |
T | 1 | a0001c0001t0001g0297 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-218-647_-218-608d others(42): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214173 | ||||||
| chr7:74214174 | ATG | A | 6 | a0001c0001t0001g0056 a0001c0001t0001g0097 a0001c0001t0001g0115 others(3): Show |
6 | HG01361.hp2 HG01928.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218-647_-218-646d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214174 | |||||||
| chr7:74214176 | G | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(2): Show |
5 | HG01081.hp2 HG01243.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-218-646G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214176 | |||||||
| chr7:74214177 | AAAATATA others(3): Show |
A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0291 |
2 | HG01346.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-218-633_-218-624d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214177 | ||||||
| chr7:74214179 | A | T | 12 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(9): Show |
12 | HG01081.hp2 HG01243.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.-218-643A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214179 | |||||||
| chr7:74214187 | T | TATGAAAA others(63): Show |
1 | a0001c0001t0001g0240 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-218-634_-218-633i others(72): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214187 | ||||||
| chr7:74214187 | T | TGA | 49 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0097 others(46): Show |
49 | HG00741.hp2 HG01069.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-218-635_-218-634i others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214187 | |||||||
| chr7:74214188 | A | ATG | 4 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG01081.hp2 HG01243.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-634_-218-633i others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214188 | |||||||
| chr7:74214188 | A | G | 2 | a0001c0001t0001g0270 a0004c0009t0001g0036 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-218-634A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214188 | |||||||
| chr7:74214189 | A | AAAAT | 3 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 |
3 | HG02630.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-218-632_-218-631i others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214189 | ||||||
| chr7:74214191 | T | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218-631T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214191 | |||||||
| chr7:74214200 | G | A | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(4): Show |
7 | HG01081.hp2 HG01243.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218-622G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214200 | |||||||
| chr7:74214201 | A | T | 1 | a0001c0002t0001g0029 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-218-621A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214201 | |||||||
| chr7:74214203 | A | AAT | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG02083.hp1 HG02135.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-218-612_-218-611d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214203 | ||||||
| chr7:74214203 | A | AATATATA others(37): Show |
2 | a0001c0002t0001g0027 a0001c0002t0001g0028 |
2 | HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-218-611_-218-610i others(46): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214203 | ||||||
| chr7:74214203 | A | AATATATA others(9): Show |
1 | a0001c0001t0001g0283 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-218-611_-218-610i others(18): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214203 | ||||||
| chr7:74214203 | A | T | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(4): Show |
7 | HG01081.hp2 HG01243.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218-619A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214203 | |||||||
| chr7:74214203 | AATATATA others(7): Show |
A | 1 | a0001c0001t0001g0168 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-218-598_-218-585d others(16): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214203 | ||||||
| chr7:74214211 | TGA | T | 9 | a0001c0001t0001g0056 a0001c0001t0001g0097 a0001c0001t0001g0098 others(6): Show |
9 | HG01361.hp2 HG01928.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.-218-610_-218-609d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214211 | |||||||
| chr7:74214212 | G | A | 1 | a0001c0002t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-218-610G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214212 | |||||||
| chr7:74214213 | A | AAAATATA others(3): Show |
3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG02083.hp1 HG02135.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-218-607_-218-598d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214213 | ||||||
| chr7:74214215 | A | AAT | 4 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG01243.hp2 HG02451.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-598_-218-597d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214215 | ||||||
| chr7:74214217 | T | TATATATG others(3): Show |
1 | a0001c0001t0001g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-218-599_-218-598i others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214217 | ||||||
| chr7:74214226 | G | A | 45 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0225 others(42): Show |
45 | HG00741.hp2 HG01069.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-218-596G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214226 | |||||||
| chr7:74214227 | A | AAT | 30 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0225 others(27): Show |
30 | HG00741.hp2 HG01069.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-218-594_-218-593i others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214227 | ||||||
| chr7:74214229 | A | AATATATA others(119): Show |
1 | a0001c0002t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-218-585_-218-584i others(128): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214229 | ||||||
| chr7:74214229 | A | T | 50 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0182 others(47): Show |
51 | HG00741.hp2 HG01069.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.-218-593A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214229 | |||||||
| chr7:74214229 | AATATATA others(21): Show |
A | 3 | a0001c0001t0001g0181 a0001c0001t0001g0214 a0001c0001t0003g0037 |
3 | HG01074.hp2 HG02040.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-218-558_-218-531d others(30): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214229 | ||||||
| chr7:74214231 | TATATATG others(43): Show |
T | 1 | a0001c0001t0001g0270 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-218-584_-218-535d others(52): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214231 | ||||||
| chr7:74214250 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 |
3 | HG01243.hp2 HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-218-572A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214250 | |||||||
| chr7:74214251 | T | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 |
3 | HG01243.hp2 HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-218-571T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214251 | |||||||
| chr7:74214252 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0070 others(17): Show |
20 | HG00438.hp1 HG01255.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.-218-570A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214252 | |||||||
| chr7:74214253 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-218-569A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214253 | |||||||
| chr7:74214253 | AAT | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(98): Show |
105 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.-218-558_-218-557d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214253 | ||||||
| chr7:74214253 | AATAT | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 |
3 | HG01243.hp2 HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-218-560_-218-557d others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214253 | ||||||
| chr7:74214254 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-218-568A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214254 | |||||||
| chr7:74214255 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-218-567T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214255 | |||||||
| chr7:74214255 | T | TATATATA others(17): Show |
2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-218-559_-218-558i others(26): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214255 | ||||||
| chr7:74214255 | TATATATA others(19): Show |
T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0083 others(3): Show |
6 | HG01884.hp1 HG02015.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218-504_-218-479d others(28): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214255 | ||||||
| chr7:74214257 | T | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0056 others(15): Show |
18 | HG00438.hp1 HG01361.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-218-565T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214257 | |||||||
| chr7:74214263 | T | C | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-559T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214263 | |||||||
| chr7:74214264 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-218-558A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214264 | |||||||
| chr7:74214265 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-218-557T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214265 | |||||||
| chr7:74214266 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-218-556G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214266 | |||||||
| chr7:74214267 | AAAATATA others(5): Show |
A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0089 |
2 | HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-218-542_-218-531d others(14): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214267 | ||||||
| chr7:74214269 | A | T | 1 | a0001c0001t0001g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-218-553A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214269 | |||||||
| chr7:74214280 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG01255.hp2 HG02258.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-218-542A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214280 | |||||||
| chr7:74214281 | A | AAT | 23 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0033 others(20): Show |
24 | HG00438.hp1 HG01081.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.-218-532_-218-531d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214281 | ||||||
| chr7:74214281 | A | T | 1 | a0001c0001t0001g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-218-541A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214281 | |||||||
| chr7:74214283 | T | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0098 a0001c0001t0001g0099 |
3 | HG02258.hp2 NA18955.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-218-539T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214283 | |||||||
| chr7:74214284 | A | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0312 |
2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-218-538A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214284 | |||||||
| chr7:74214295 | A | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0240 |
2 | HG01496.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-218-527A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214295 | |||||||
| chr7:74214305 | T | TATATATA others(48): Show |
1 | a0001c0001t0001g0310 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-218-516_-218-515i others(57): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214305 | ||||||
| chr7:74214305 | TAA | T | 3 | a0001c0001t0001g0238 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG01346.hp1 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.-218-515_-218-514d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214305 | ||||||
| chr7:74214306 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-218-516A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214306 | |||||||
| chr7:74214307 | A | AAT | 19 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0034 others(16): Show |
19 | HG00140.hp1 HG00558.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-218-506_-218-505d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214307 | ||||||
| chr7:74214307 | A | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0287 a0001c0001t0001g0310 |
3 | HG01175.hp2 HG01978.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-218-515A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214307 | |||||||
| chr7:74214307 | AATATATA others(21): Show |
A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0150 others(4): Show |
7 | HG01433.hp1 HG02040.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218-394_-218-367d others(30): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214307 | ||||||
| chr7:74214307 | AATATATA others(49): Show |
A | 1 | a0001c0001t0001g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-218-422_-218-367d others(58): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214307 | ||||||
| chr7:74214321 | A | C | 10 | a0001c0001t0001g0228 a0001c0001t0001g0238 a0001c0001t0001g0240 others(7): Show |
10 | HG01175.hp2 HG01346.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-218-501A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214321 | |||||||
| chr7:74214333 | A | T | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG01106.hp2 HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-218-489A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214333 | |||||||
| chr7:74214333 | AAT | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
89 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-218-478_-218-477d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214333 | ||||||
| chr7:74214333 | AATATATA others(23): Show |
A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0118 a0001c0001t0001g0173 |
3 | HG02132.hp1 NA18945.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-218-478_-218-449d others(32): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214333 | ||||||
| chr7:74214333 | AATATATA others(51): Show |
A | 1 | a0001c0001t0001g0014 | 2 | NA18977.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-218-478_-218-421d others(60): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214333 | ||||||
| chr7:74214333 | AATATATA others(79): Show |
A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | NA18955.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-218-478_-218-393d others(88): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214333 | ||||||
| chr7:74214335 | T | TATATATA others(71): Show |
1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-480_-218-479i others(80): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214335 | ||||||
| chr7:74214349 | A | C | 24 | a0001c0001t0001g0023 a0001c0001t0001g0228 a0001c0001t0001g0233 others(21): Show |
25 | HG01106.hp2 HG01175.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.-218-473A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214349 | |||||||
| chr7:74214349 | AAT | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0100 a0001c0001t0001g0241 |
3 | HG02523.hp2 HG02698.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-218-463_-218-462d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214349 | ||||||
| chr7:74214351 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-218-471T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214351 | |||||||
| chr7:74214355 | TATATAA | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0264 a0001c0001t0001g0265 others(3): Show |
7 | HG01106.hp2 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218-461_-218-456d others(8): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214355 | ||||||
| chr7:74214357 | TATAA | T | 18 | a0001c0001t0001g0191 a0001c0001t0001g0239 a0001c0001t0001g0256 others(15): Show |
18 | HG01069.hp1 HG01081.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.-218-461_-218-458d others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214357 | ||||||
| chr7:74214359 | TAA | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0233 a0001c0001t0001g0234 others(4): Show |
7 | HG02027.hp1 HG02683.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218-461_-218-460d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214359 | ||||||
| chr7:74214361 | A | AATATATA others(17): Show |
1 | a0001c0001t0001g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-218-446_-218-445i others(26): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214361 | ||||||
| chr7:74214361 | AAT | A | 39 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0060 others(36): Show |
40 | HG00558.hp1 HG00738.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.-218-450_-218-449d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214361 | ||||||
| chr7:74214377 | A | AATATATA others(15): Show |
1 | a0001c0001t0001g0230 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-218-434_-218-433i others(24): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214377 | ||||||
| chr7:74214377 | A | C | 64 | a0001c0001t0001g0023 a0001c0001t0001g0180 a0001c0001t0001g0183 others(61): Show |
65 | HG00741.hp2 HG01069.hp1 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.-218-445A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214377 | |||||||
| chr7:74214383 | TATATAA | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0302 |
3 | HG01070.hp1 HG01071.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-218-433_-218-428d others(8): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214383 | ||||||
| chr7:74214389 | AAT | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0038 others(29): Show |
33 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-218-422_-218-421d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214389 | ||||||
| chr7:74214389 | AATATATA others(23): Show |
A | 3 | a0001c0003t0001g0052 a0001c0003t0001g0054 a0001c0003t0001g0067 |
3 | HG00597.hp2 HG02015.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.-218-422_-218-393d others(32): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214389 | ||||||
| chr7:74214391 | T | A | 1 | a0001c0001t0003g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-218-431T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214391 | |||||||
| chr7:74214400 | A | G | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-422A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214400 | |||||||
| chr7:74214405 | A | C | 73 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(70): Show |
76 | HG00741.hp2 HG01069.hp1 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.-218-417A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214405 | |||||||
| chr7:74214417 | AAT | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(25): Show |
31 | HG00673.hp1 HG01123.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.-218-394_-218-393d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214417 | ||||||
| chr7:74214419 | T | A | 1 | a0001c0001t0003g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-218-403T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214419 | |||||||
| chr7:74214419 | T | TATATATA others(375): Show |
1 | a0001c0002t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-218-355_-218-354i others(384): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214419 | ||||||
| chr7:74214419 | TATATATA others(19): Show |
T | 12 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0044 others(9): Show |
12 | HG00280.hp1 HG00323.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.-218-366_-218-341d others(28): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214419 | ||||||
| chr7:74214428 | A | G | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-394A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214428 | |||||||
| chr7:74214433 | A | C | 79 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(76): Show |
82 | HG00741.hp2 HG01069.hp1 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.-218-389A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214433 | |||||||
| chr7:74214433 | AAT | A | 7 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | HG01175.hp2 HG01346.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218-379_-218-378d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214433 | ||||||
| chr7:74214435 | TATATATA others(17): Show |
T | 1 | a0001c0001t0001g0100 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-218-377_-218-354d others(26): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214435 | ||||||
| chr7:74214441 | TATAAATA others(111): Show |
T | 1 | a0001c0001t0001g0042 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-218-377_-218-260d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214441 | ||||||
| chr7:74214443 | T | A | 4 | a0001c0001t0001g0301 a0001c0003t0001g0052 a0001c0003t0001g0054 others(1): Show |
4 | HG00597.hp2 HG02015.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-379T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214443 | |||||||
| chr7:74214443 | T | G | 1 | a0001c0001t0001g0090 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-218-379T>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214443 | |||||||
| chr7:74214443 | TAAATATA others(107): Show |
T | 1 | a0001c0001t0001g0242 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-218-366_-218-253d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214443 | ||||||
| chr7:74214445 | A | AAT | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
96 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-218-368_-218-367d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214445 | ||||||
| chr7:74214445 | A | AATATATA others(375): Show |
1 | a0001c0002t0001g0029 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-218-341_-218-340i others(384): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214445 | ||||||
| chr7:74214445 | A | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0301 a0001c0003t0001g0052 others(2): Show |
5 | HG00597.hp2 HG02015.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-377A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214445 | |||||||
| chr7:74214447 | TATATATA others(133): Show |
T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(5): Show |
12 | HG02723.hp2 HG03195.hp1 HG03831.hp2 others(9): Show |
intron_variant | MODIFIER | c.-218-366_-218-227d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214447 | ||||||
| chr7:74214449 | TATATATG others(167): Show |
T | 1 | a0001c0001t0001g0090 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-218-366_-218-193d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214449 | ||||||
| chr7:74214456 | G | A | 5 | a0001c0001t0001g0228 a0001c0001t0001g0238 a0001c0001t0001g0287 others(2): Show |
5 | HG01358.hp2 HG01975.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-366G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214456 | |||||||
| chr7:74214457 | A | T | 5 | a0001c0001t0001g0228 a0001c0001t0001g0238 a0001c0001t0001g0287 others(2): Show |
5 | HG01358.hp2 HG01975.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-365A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214457 | |||||||
| chr7:74214458 | A | G | 5 | a0001c0001t0001g0228 a0001c0001t0001g0238 a0001c0001t0001g0287 others(2): Show |
5 | HG01358.hp2 HG01975.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-364A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214458 | |||||||
| chr7:74214458 | AAATATAT others(157): Show |
A | 1 | a0001c0001t0001g0178 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-218-351_-218-188d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214458 | ||||||
| chr7:74214459 | A | AAT | 5 | a0001c0001t0001g0041 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
5 | HG00673.hp1 HG01123.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-353_-218-352d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214459 | ||||||
| chr7:74214459 | A | C | 34 | a0001c0001t0001g0022 a0001c0001t0001g0218 a0001c0001t0001g0230 others(31): Show |
35 | HG01109.hp1 HG01515.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.-218-363A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214459 | |||||||
| chr7:74214459 | AATATATA others(7): Show |
A | 1 | a0001c0001t0001g0179 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-218-352_-218-339d others(16): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214459 | ||||||
| chr7:74214461 | T | A | 5 | a0001c0001t0001g0228 a0001c0001t0001g0238 a0001c0001t0001g0287 others(2): Show |
5 | HG01358.hp2 HG01975.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-361T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214461 | |||||||
| chr7:74214461 | TATATATA others(3): Show |
T | 1 | a0001c0001t0003g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-218-351_-218-342d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214461 | ||||||
| chr7:74214461 | TATATATA others(155): Show |
T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0184 |
3 | NA18943.hp1 NA18970.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-218-351_-218-190d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214461 | ||||||
| chr7:74214471 | A | AAT | 3 | a0001c0001t0001g0240 a0001c0001t0001g0289 a0001c0001t0001g0310 |
3 | HG01175.hp2 HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-218-340_-218-339d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214471 | ||||||
| chr7:74214471 | AAT | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(48): Show |
51 | HG00639.hp1 HG00642.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.-218-340_-218-339d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214471 | ||||||
| chr7:74214471 | AATATATA others(83): Show |
A | 1 | a0001c0001t0001g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-218-340_-218-251d others(92): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214471 | ||||||
| chr7:74214473 | T | A | 2 | a0001c0001t0001g0040 a0001c0003t0001g0051 |
2 | HG00558.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-218-349T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214473 | |||||||
| chr7:74214473 | TATATATA others(107): Show |
T | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(5): Show |
8 | HG00438.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.-218-325_-218-212d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214473 | ||||||
| chr7:74214481 | TATGAAAA others(87): Show |
T | 1 | a0001c0001t0001g0058 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-218-338_-218-245d others(96): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214481 | ||||||
| chr7:74214482 | A | G | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-340A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214482 | |||||||
| chr7:74214485 | A | AAAATATA others(3): Show |
2 | a0001c0001t0001g0300 a0001c0001t0001g0304 |
2 | HG01168.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-218-335_-218-326d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214485 | ||||||
| chr7:74214487 | A | C | 21 | a0001c0001t0001g0022 a0001c0001t0001g0218 a0001c0001t0001g0231 others(18): Show |
22 | HG01515.hp1 HG01891.hp2 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-218-335A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214487 | |||||||
| chr7:74214487 | AAT | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-325_-218-324d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214487 | ||||||
| chr7:74214489 | T | A | 1 | a0001c0001t0001g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-218-333T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214489 | |||||||
| chr7:74214489 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-218-333T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214489 | |||||||
| chr7:74214489 | TATATATA others(127): Show |
T | 1 | a0001c0001t0001g0223 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-218-323_-218-190d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214489 | ||||||
| chr7:74214495 | TATAA | T | 17 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.-218-323_-218-320d others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214495 | ||||||
| chr7:74214498 | A | G | 2 | a0001c0001t0001g0300 a0001c0001t0001g0304 |
2 | HG01168.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-218-324A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214498 | |||||||
| chr7:74214498 | AAATATAT others(51): Show |
A | 1 | a0001c0001t0001g0087 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-218-321_-218-264d others(60): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214498 | ||||||
| chr7:74214499 | A | AAT | 9 | a0001c0001t0001g0040 a0001c0001t0001g0228 a0001c0001t0001g0238 others(6): Show |
9 | HG00558.hp1 HG01358.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.-218-312_-218-311d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214499 | ||||||
| chr7:74214499 | AAT | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0038 others(29): Show |
33 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.-218-312_-218-311d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214499 | ||||||
| chr7:74214499 | AATATATA others(55): Show |
A | 13 | a0001c0001t0001g0097 a0001c0001t0001g0109 a0001c0001t0001g0110 others(10): Show |
13 | HG00438.hp2 HG00738.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.-218-312_-218-251d others(64): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214499 | ||||||
| chr7:74214501 | T | A | 19 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0121 others(16): Show |
19 | HG01168.hp2 HG01243.hp1 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.-218-321T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214501 | |||||||
| chr7:74214501 | TATATATA others(79): Show |
T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0074 a0001c0001t0001g0154 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218-217_-218-132d others(88): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214501 | ||||||
| chr7:74214505 | TATATATG others(3): Show |
T | 1 | a0001c0001t0001g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-218-310_-218-301d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214505 | ||||||
| chr7:74214510 | A | G | 16 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0173 others(13): Show |
17 | HG01891.hp2 HG02074.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-218-312A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214510 | |||||||
| chr7:74214511 | T | A | 15 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0173 others(12): Show |
16 | HG01891.hp2 HG02074.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.-218-311T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214511 | |||||||
| chr7:74214512 | G | A | 18 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0173 others(15): Show |
19 | HG01168.hp2 HG01515.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-218-310G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214512 | |||||||
| chr7:74214513 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-218-309A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214513 | |||||||
| chr7:74214514 | AAATATAT others(101): Show |
A | 1 | a0001c0001t0006g0203 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-218-297_-218-190d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214514 | ||||||
| chr7:74214515 | A | AAT | 6 | a0001c0001t0001g0014 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
7 | HG03471.hp2 HG03540.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218-299_-218-298d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214515 | ||||||
| chr7:74214515 | A | T | 18 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0173 others(15): Show |
19 | HG01168.hp2 HG01515.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-218-307A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214515 | |||||||
| chr7:74214515 | AATATATA others(107): Show |
A | 2 | a0001c0001t0001g0040 a0001c0003t0001g0051 |
2 | HG00558.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-218-297_-218-184d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214515 | ||||||
| chr7:74214517 | TATATATA others(51): Show |
T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG00673.hp2 HG02523.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218-297_-218-240d others(60): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214517 | ||||||
| chr7:74214517 | TATATATA others(99): Show |
T | 10 | a0001c0001t0001g0017 a0001c0001t0001g0121 a0001c0001t0001g0127 others(7): Show |
10 | HG01928.hp1 HG01952.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-218-297_-218-192d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214517 | ||||||
| chr7:74214519 | TATATAAA others(11): Show |
T | 1 | a0001c0001t0001g0227 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-218-297_-218-280d others(20): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214519 | ||||||
| chr7:74214519 | TATATAAA others(75): Show |
T | 1 | a0001c0001t0001g0172 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-218-297_-218-216d others(84): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214519 | ||||||
| chr7:74214519 | TATATAAA others(97): Show |
T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0198 |
3 | NA18944.hp1 NA19066.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-218-297_-218-194d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214519 | ||||||
| chr7:74214523 | T | TATAA | 9 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
9 | HG01243.hp2 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-218-298_-218-297i others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214523 | ||||||
| chr7:74214523 | T | TATAAATA others(11): Show |
1 | a0001c0002t0001g0029 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-218-298_-218-297i others(20): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214523 | ||||||
| chr7:74214523 | T | TATAAATA others(535): Show |
1 | a0001c0002t0001g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-218-298_-218-297i others(544): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214523 | ||||||
| chr7:74214523 | T | TATAAATA others(535): Show |
1 | a0001c0002t0001g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-218-298_-218-297i others(544): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214523 | ||||||
| chr7:74214523 | TAAATATA others(27): Show |
T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0107 others(1): Show |
4 | HG00323.hp2 HG01255.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-286_-218-253d others(36): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214523 | ||||||
| chr7:74214524 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-218-298A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214524 | |||||||
| chr7:74214524 | AAATATAT others(25): Show |
A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0092 others(20): Show |
24 | HG00639.hp1 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.-218-295_-218-264d others(34): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214524 | ||||||
| chr7:74214524 | AAATATAT others(111): Show |
A | 1 | a0001c0001t0003g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-218-295_-218-178d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214524 | ||||||
| chr7:74214525 | A | AAT | 13 | a0001c0001t0001g0022 a0001c0001t0001g0218 a0001c0001t0001g0231 others(10): Show |
14 | HG01891.hp2 HG02074.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.-218-288_-218-287d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214525 | ||||||
| chr7:74214525 | A | T | 29 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0034 others(26): Show |
29 | HG00140.hp1 HG01175.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-218-297A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214525 | |||||||
| chr7:74214525 | AATATATA others(9): Show |
A | 1 | a0001c0001t0001g0039 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-218-286_-218-271d others(18): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214525 | ||||||
| chr7:74214525 | AATATATA others(29): Show |
A | 1 | a0001c0001t0001g0062 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-218-283_-218-248d others(38): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214525 | ||||||
| chr7:74214525 | AATATATA others(99): Show |
A | 1 | a0001c0001t0001g0190 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-218-283_-218-178d others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214525 | ||||||
| chr7:74214527 | T | A | 19 | a0001c0001t0001g0033 a0001c0001t0001g0108 a0001c0001t0001g0115 others(16): Show |
19 | HG00140.hp1 HG01175.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.-218-295T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214527 | |||||||
| chr7:74214533 | TATGA | T | 5 | a0001c0001t0001g0232 a0001c0001t0001g0282 a0001c0001t0001g0284 others(2): Show |
5 | HG02809.hp2 HG04199.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-286_-218-283d others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214533 | ||||||
| chr7:74214535 | TGA | T | 10 | a0001c0001t0001g0033 a0001c0001t0001g0108 a0001c0001t0001g0115 others(7): Show |
10 | HG00140.hp1 HG01175.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.-218-286_-218-285d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214535 | |||||||
| chr7:74214536 | G | A | 11 | a0001c0001t0001g0194 a0001c0001t0001g0238 a0001c0001t0001g0240 others(8): Show |
11 | HG01081.hp2 HG01168.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-218-286G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214536 | |||||||
| chr7:74214536 | GAATATAT others(31): Show |
G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0075 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-218-273_-218-236d others(40): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214536 | ||||||
| chr7:74214537 | A | AAAAT | 8 | a0001c0001t0001g0089 a0001c0001t0001g0120 a0001c0001t0001g0143 others(5): Show |
8 | HG01433.hp2 HG01496.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-218-284_-218-283i others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214537 | ||||||
| chr7:74214537 | A | AAAATAT | 6 | a0001c0001t0001g0032 a0001c0001t0001g0182 a0001c0001t0001g0241 others(3): Show |
6 | HG02258.hp2 HG03209.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218-284_-218-283i others(8): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214537 | ||||||
| chr7:74214537 | A | AAAATATA others(1): Show |
17 | a0001c0001t0001g0022 a0001c0001t0001g0218 a0001c0001t0001g0231 others(14): Show |
18 | HG01891.hp2 HG02074.hp2 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.-218-284_-218-283i others(10): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214537 | ||||||
| chr7:74214537 | A | AAAATATA others(3): Show |
4 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-284_-218-283i others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214537 | ||||||
| chr7:74214537 | A | T | 5 | a0001c0001t0001g0194 a0001c0001t0001g0238 a0001c0001t0001g0240 others(2): Show |
5 | HG01496.hp1 HG01975.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-285A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214537 | |||||||
| chr7:74214537 | AATATATA others(81): Show |
A | 1 | a0001c0001t0001g0119 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-218-268_-218-181d others(90): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214537 | ||||||
| chr7:74214538 | ATATATAT others(77): Show |
A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(21): Show |
27 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.-218-283_-218-200d others(86): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214538 | |||||||
| chr7:74214539 | T | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(132): Show |
140 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.-218-283T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214539 | |||||||
| chr7:74214540 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-218-282A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214540 | |||||||
| chr7:74214541 | T | A | 7 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218-281T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214541 | |||||||
| chr7:74214541 | TATATATA others(75): Show |
T | 42 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(39): Show |
43 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.-218-266_-218-185d others(84): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214541 | ||||||
| chr7:74214542 | A | G | 12 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0001t0001g0222 others(9): Show |
12 | HG00140.hp1 HG01175.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.-218-280A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214542 | |||||||
| chr7:74214543 | T | A | 31 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0108 others(28): Show |
32 | HG00140.hp1 HG01175.hp2 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.-218-279T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214543 | |||||||
| chr7:74214543 | TATATATA others(73): Show |
T | 6 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0131 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218-266_-218-187d others(82): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214543 | ||||||
| chr7:74214544 | A | G | 6 | a0001c0001t0001g0033 a0001c0001t0001g0232 a0001c0001t0001g0282 others(3): Show |
6 | HG02809.hp2 HG02818.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218-278A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214544 | |||||||
| chr7:74214545 | T | A | 21 | a0001c0001t0001g0033 a0001c0001t0001g0108 a0001c0001t0001g0115 others(18): Show |
21 | HG00140.hp1 HG01175.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.-218-277T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214545 | |||||||
| chr7:74214545 | T | TATATAAA others(17): Show |
9 | a0001c0001t0001g0191 a0001c0001t0001g0233 a0001c0001t0001g0257 others(6): Show |
9 | HG01952.hp2 HG01981.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-218-272_-218-271i others(26): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214545 | ||||||
| chr7:74214545 | T | TATATAAA others(47): Show |
8 | a0001c0001t0001g0180 a0001c0001t0001g0234 a0001c0001t0001g0236 others(5): Show |
8 | HG01993.hp2 HG02683.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-218-272_-218-271i others(56): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214545 | ||||||
| chr7:74214545 | T | TATATAAA others(77): Show |
1 | a0001c0001t0001g0239 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-218-272_-218-271i others(86): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214545 | ||||||
| chr7:74214545 | T | TATATAAA others(45): Show |
9 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0225 others(6): Show |
11 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-218-272_-218-271i others(54): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214545 | ||||||
| chr7:74214545 | T | TATATAAA others(45): Show |
2 | a0001c0001t0001g0230 a0001c0001t0001g0235 |
2 | HG02027.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-218-272_-218-271i others(54): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214545 | ||||||
| chr7:74214545 | TATATATA others(71): Show |
T | 1 | a0001c0001t0001g0298 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-218-266_-218-189d others(80): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214545 | ||||||
| chr7:74214545 | TATATATA others(79): Show |
T | 1 | a0001c0001t0001g0210 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-218-217_-218-132d others(88): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214545 | ||||||
| chr7:74214545 | TATATATA others(93): Show |
T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0153 |
3 | HG03239.hp2 HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-218-266_-218-167d others(102): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214545 | ||||||
| chr7:74214547 | T | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0232 a0001c0001t0001g0282 others(3): Show |
6 | HG02809.hp2 HG02818.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218-275T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214547 | |||||||
| chr7:74214547 | TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0064 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-218-273_-218-264d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214547 | ||||||
| chr7:74214547 | TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0283 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-218-266_-218-255d others(14): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214547 | ||||||
| chr7:74214548 | ATATATAT others(1): Show |
A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0061 a0001c0001t0001g0063 others(2): Show |
5 | HG00673.hp1 HG01123.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-273_-218-266d others(10): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214548 | |||||||
| chr7:74214549 | TATATATG others(1): Show |
T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0046 a0001c0001t0001g0098 others(6): Show |
10 | HG02602.hp1 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-218-271_-218-264d others(10): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214549 | ||||||
| chr7:74214550 | ATATATG | A | 33 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0044 others(30): Show |
33 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.-218-271_-218-266d others(8): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214550 | |||||||
| chr7:74214551 | T | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0055 others(2): Show |
6 | HG00621.hp1 HG01515.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218-271T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214551 | |||||||
| chr7:74214553 | TATGAAAA others(27): Show |
T | 1 | a0001c0001t0001g0212 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-218-266_-218-233d others(36): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214553 | ||||||
| chr7:74214555 | TGAAA | T | 10 | a0001c0001t0001g0033 a0001c0001t0001g0108 a0001c0001t0001g0115 others(7): Show |
10 | HG00140.hp1 HG01361.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-218-266_-218-263d others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214555 | |||||||
| chr7:74214555 | TGAAAATA others(25): Show |
T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0055 |
4 | HG00621.hp1 HG02280.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-266_-218-235d others(34): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214555 | |||||||
| chr7:74214556 | G | A | 43 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0180 others(40): Show |
45 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.-218-266G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214556 | |||||||
| chr7:74214557 | A | AAAATATA others(5): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0302 |
2 | HG01109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-218-263_-218-252d others(14): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214557 | ||||||
| chr7:74214557 | A | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0087 others(26): Show |
30 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.-218-265A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214557 | |||||||
| chr7:74214558 | A | G | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-264A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214558 | |||||||
| chr7:74214559 | A | T | 81 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0024 others(78): Show |
83 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-218-263A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214559 | |||||||
| chr7:74214559 | AATATATA others(63): Show |
A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0047 |
2 | HG02145.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-218-235_-218-166d others(72): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214559 | ||||||
| chr7:74214561 | T | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0042 others(15): Show |
18 | HG00140.hp1 HG00323.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-218-261T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214561 | |||||||
| chr7:74214561 | T | TATATATA others(1): Show |
20 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0034 others(17): Show |
21 | HG01243.hp2 HG01891.hp2 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-218-254_-218-253i others(10): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214561 | ||||||
| chr7:74214561 | T | TATATATA others(3): Show |
1 | a0001c0002t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-218-252_-218-251i others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214561 | ||||||
| chr7:74214561 | TATATATA others(55): Show |
T | 1 | a0001c0001t0001g0186 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-218-250_-218-189d others(64): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214561 | ||||||
| chr7:74214572 | G | A | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-250G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214572 | |||||||
| chr7:74214575 | A | T | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-247A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214575 | |||||||
| chr7:74214575 | AAT | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(20): Show |
24 | HG00642.hp1 HG01106.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-218-237_-218-236d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214575 | ||||||
| chr7:74214575 | AATATATA others(47): Show |
A | 21 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0043 others(18): Show |
21 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.-218-235_-218-182d others(56): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214575 | ||||||
| chr7:74214577 | T | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0073 a0001c0001t0001g0075 |
3 | HG00609.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-218-245T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214577 | |||||||
| chr7:74214577 | TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0182 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-218-235_-218-226d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214577 | ||||||
| chr7:74214583 | T | TAA | 3 | a0001c0001t0001g0248 a0001c0001t0001g0282 a0001c0001t0001g0301 |
3 | HG02809.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-218-238_-218-237i others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214583 | ||||||
| chr7:74214585 | T | A | 8 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0080 others(5): Show |
8 | HG00673.hp2 HG02523.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.-218-237T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214585 | |||||||
| chr7:74214587 | A | AAT | 30 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0087 others(27): Show |
30 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.-218-226_-218-225d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214587 | ||||||
| chr7:74214587 | A | AATAT | 59 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(56): Show |
62 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.-218-228_-218-225d others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214587 | ||||||
| chr7:74214587 | A | T | 12 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0080 others(9): Show |
12 | HG00673.hp2 HG02523.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.-218-235A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214587 | |||||||
| chr7:74214591 | TATATATG others(3): Show |
T | 1 | a0001c0001t0001g0097 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-218-224_-218-215d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214591 | ||||||
| chr7:74214591 | TATATATG others(13): Show |
T | 16 | a0001c0001t0001g0042 a0001c0001t0001g0229 a0001c0001t0001g0237 others(13): Show |
16 | HG00741.hp2 HG01123.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.-218-224_-218-205d others(22): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214591 | ||||||
| chr7:74214593 | TATATGAA others(1): Show |
T | 4 | a0001c0001t0001g0238 a0001c0001t0001g0260 a0001c0001t0001g0290 others(1): Show |
4 | HG01975.hp2 HG02148.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-224_-218-217d others(10): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214593 | ||||||
| chr7:74214594 | A | T | 3 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 |
3 | HG02630.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-218-228A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214594 | |||||||
| chr7:74214595 | TATGAAA | T | 3 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0309 |
3 | HG02896.hp2 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-218-224_-218-219d others(8): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214595 | ||||||
| chr7:74214598 | G | A | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-224G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214598 | |||||||
| chr7:74214600 | AAATATAT others(15): Show |
A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0162 others(3): Show |
6 | HG00642.hp1 HG01106.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218-211_-218-190d others(24): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214600 | ||||||
| chr7:74214601 | A | AAT | 55 | a0001c0001t0001g0024 a0001c0001t0001g0031 a0001c0001t0001g0033 others(52): Show |
56 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.-218-213_-218-212d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214601 | ||||||
| chr7:74214601 | A | T | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-221A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214601 | |||||||
| chr7:74214601 | AAT | A | 3 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 |
3 | HG02630.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-218-213_-218-212d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214601 | ||||||
| chr7:74214601 | AATATATA others(17): Show |
A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0075 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-218-211_-218-188d others(26): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214601 | ||||||
| chr7:74214601 | AATATATA others(21): Show |
A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0055 others(3): Show |
7 | HG00621.hp1 HG02280.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218-211_-218-184d others(30): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214601 | ||||||
| chr7:74214601 | AATATATA others(55): Show |
A | 1 | a0001c0001t0001g0017 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-218-197_-218-136d others(64): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214601 | ||||||
| chr7:74214603 | TATATATA others(13): Show |
T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0098 others(5): Show |
9 | HG01167.hp1 HG02155.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-218-211_-218-192d others(22): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214603 | ||||||
| chr7:74214604 | ATATATAA others(2): Show |
A | 6 | a0001c0001t0001g0120 a0001c0001t0001g0194 a0001c0001t0001g0227 others(3): Show |
6 | HG03139.hp1 HG03209.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218-217_-218-209d others(11): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214604 | |||||||
| chr7:74214604 | ATATATAA others(52): Show |
A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG01261.hp1 HG01433.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.-218-217_-218-159d others(61): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214604 | |||||||
| chr7:74214605 | TATATAAA others(11): Show |
T | 5 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0199 others(2): Show |
5 | HG01109.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-211_-218-194d others(20): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214605 | ||||||
| chr7:74214607 | T | TATATAA | 9 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(6): Show |
9 | HG01361.hp1 HG01952.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.-218-212_-218-211i others(8): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214607 | ||||||
| chr7:74214608 | A | G | 3 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0309 |
3 | HG02896.hp2 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-218-214A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214608 | |||||||
| chr7:74214609 | T | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0281 a0001c0001t0001g0283 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-213T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214609 | |||||||
| chr7:74214609 | TAAATATA others(7): Show |
T | 1 | a0001c0001t0001g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-218-211_-218-198d others(16): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214609 | ||||||
| chr7:74214610 | A | G | 5 | a0001c0001t0001g0097 a0001c0001t0001g0238 a0001c0001t0001g0260 others(2): Show |
5 | HG01928.hp2 HG01975.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-212A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214610 | |||||||
| chr7:74214611 | A | T | 17 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0172 others(14): Show |
19 | HG01361.hp1 HG01515.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.-218-211A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214611 | |||||||
| chr7:74214612 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0097 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-218-209_-218-200d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214612 | |||||||
| chr7:74214613 | T | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0238 a0001c0001t0001g0249 others(5): Show |
9 | HG01515.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.-218-209T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214613 | |||||||
| chr7:74214615 | T | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0253 a0001c0001t0001g0254 |
4 | HG01891.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-207T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214615 | |||||||
| chr7:74214621 | T | TATGAAAA others(51): Show |
1 | a0001c0002t0001g0029 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-218-201_-218-200i others(60): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214621 | |||||||
| chr7:74214621 | TGA | T | 6 | a0001c0001t0001g0238 a0001c0001t0001g0260 a0001c0001t0001g0281 others(3): Show |
6 | HG01975.hp2 HG02148.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218-200_-218-199d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214621 | |||||||
| chr7:74214622 | G | A | 65 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(62): Show |
68 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.-218-200G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214622 | |||||||
| chr7:74214622 | G | GAA | 20 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0070 others(17): Show |
21 | HG00438.hp1 HG01981.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.-218-199_-218-198d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214622 | ||||||
| chr7:74214623 | A | AAAAT | 29 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(26): Show |
32 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.-218-198_-218-197i others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214623 | ||||||
| chr7:74214623 | A | AAAATAT | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(4): Show |
7 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218-198_-218-197i others(8): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214623 | ||||||
| chr7:74214623 | A | AAAATATA others(3): Show |
8 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(5): Show |
8 | HG01361.hp1 HG01952.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-218-198_-218-197i others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214623 | ||||||
| chr7:74214623 | A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0264 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-218-198_-218-197i others(14): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214623 | ||||||
| chr7:74214623 | A | T | 57 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(54): Show |
60 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.-218-199A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214623 | |||||||
| chr7:74214623 | AATAT | A | 17 | a0001c0001t0001g0042 a0001c0001t0001g0229 a0001c0001t0001g0237 others(14): Show |
17 | HG00741.hp2 HG01123.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.-218-184_-218-181d others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214623 | ||||||
| chr7:74214625 | T | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0074 others(6): Show |
10 | HG00741.hp1 HG01070.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.-218-197T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214625 | |||||||
| chr7:74214626 | A | G | 56 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0058 others(53): Show |
58 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.-218-196A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214626 | |||||||
| chr7:74214627 | T | A | 72 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0058 others(69): Show |
74 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.-218-195T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214627 | |||||||
| chr7:74214629 | T | A | 73 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0042 others(70): Show |
75 | HG00609.hp1 HG00741.hp2 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.-218-193T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214629 | |||||||
| chr7:74214629 | T | TGAAA | 3 | a0001c0001t0001g0022 a0001c0001t0001g0253 a0001c0001t0001g0254 |
4 | HG01891.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-193_-218-192i others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214629 | |||||||
| chr7:74214631 | T | A | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(8): Show |
11 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-218-191T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214631 | |||||||
| chr7:74214633 | T | A | 6 | a0001c0001t0001g0120 a0001c0001t0001g0194 a0001c0001t0001g0227 others(3): Show |
6 | HG03139.hp1 HG03209.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218-189T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214633 | |||||||
| chr7:74214635 | TATATATG others(3): Show |
T | 1 | a0001c0001t0001g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-218-180_-218-171d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214635 | ||||||
| chr7:74214638 | A | T | 1 | a0001c0002t0001g0029 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-218-184A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214638 | |||||||
| chr7:74214639 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-218-183T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214639 | |||||||
| chr7:74214642 | G | A | 8 | a0001c0001t0001g0120 a0001c0001t0001g0182 a0001c0001t0001g0194 others(5): Show |
8 | HG03139.hp1 HG03209.hp2 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.-218-180G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214642 | |||||||
| chr7:74214643 | A | T | 3 | a0001c0001t0001g0182 a0001c0001t0003g0037 a0001c0002t0001g0030 |
3 | HG01074.hp2 HG03471.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-218-179A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214643 | |||||||
| chr7:74214645 | A | AAT | 3 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 |
3 | HG02630.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-218-166_-218-165d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214645 | ||||||
| chr7:74214645 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-218-177A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214645 | |||||||
| chr7:74214645 | AAT | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG03834.hp1 HG03942.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-218-166_-218-165d others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214645 | ||||||
| chr7:74214647 | T | A | 1 | a0001c0001t0001g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-218-175T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214647 | |||||||
| chr7:74214647 | T | TATATATA others(3): Show |
5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(2): Show |
5 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-218-166_-218-165i others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214647 | ||||||
| chr7:74214649 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-218-173T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214649 | |||||||
| chr7:74214649 | TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0194 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-218-171_-218-162d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214649 | ||||||
| chr7:74214650 | ATATATAT others(32): Show |
A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0227 a0001c0001t0001g0241 |
3 | HG03139.hp1 NA18983.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-218-171_-218-133d others(41): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214650 | |||||||
| chr7:74214651 | T | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-218-171T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214651 | |||||||
| chr7:74214658 | G | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0243 a0001c0001t0001g0244 |
3 | HG03209.hp2 HG03540.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-218-164G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214658 | |||||||
| chr7:74214659 | A | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-218-163A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214659 | |||||||
| chr7:74214663 | T | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-218-159T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214663 | |||||||
| chr7:74214663 | T | TATATATA others(20): Show |
1 | a0001c0001t0001g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-218-139_-218-113d others(29): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214663 | ||||||
| chr7:74214667 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-218-155T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214667 | |||||||
| chr7:74214671 | T | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0243 a0001c0001t0001g0244 |
3 | HG03209.hp2 HG03540.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-218-151T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214671 | |||||||
| chr7:74214673 | A | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0243 a0001c0001t0001g0244 |
3 | HG03209.hp2 HG03540.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-218-149A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214673 | |||||||
| chr7:74214677 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-218-145T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214677 | |||||||
| chr7:74214679 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-218-143T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214679 | |||||||
| chr7:74214684 | G | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0243 a0001c0001t0001g0244 |
3 | HG03209.hp2 HG03540.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-218-138G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214684 | |||||||
| chr7:74214685 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-218-137A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214685 | |||||||
| chr7:74214686 | A | T | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-136A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214686 | |||||||
| chr7:74214687 | A | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-218-135A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214687 | |||||||
| chr7:74214687 | A | G | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-135A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214687 | |||||||
| chr7:74214687 | A | T | 1 | a0001c0001t0001g0194 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-218-135A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214687 | |||||||
| chr7:74214688 | AT | A | 4 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(1): Show |
4 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-133delT | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214688 | |||||||
| chr7:74214689 | T | A | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-133T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214689 | |||||||
| chr7:74214689 | TA | T | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
7 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218-131delA | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214689 | ||||||
| chr7:74214689 | TAATATAT others(3): Show |
T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(32): Show |
36 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.-218-110_-218-101d others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214689 | ||||||
| chr7:74214689 | TAATATAT others(4): Show |
T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-218-131_-218-121d others(13): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214689 | ||||||
| chr7:74214702 | T | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0227 a0001c0001t0001g0241 |
3 | HG03139.hp1 NA18983.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-218-120T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214702 | |||||||
| chr7:74214702 | T | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0194 |
2 | HG03669.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-218-120T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214702 | |||||||
| chr7:74214708 | T | TATATGA | 3 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 |
3 | HG01081.hp2 HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-218-113_-218-112i others(8): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214708 | ||||||
| chr7:74214710 | A | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(2): Show |
5 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-218-112A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214710 | |||||||
| chr7:74214711 | A | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(2): Show |
5 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-218-111A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214711 | |||||||
| chr7:74214712 | T | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218-110T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214712 | |||||||
| chr7:74214714 | T | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(2): Show |
5 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-218-108T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214714 | |||||||
| chr7:74214717 | AT | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(2): Show |
5 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-218-104delT | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214717 | |||||||
| chr7:74214718 | TAAAA | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0120 a0001c0001t0001g0227 others(1): Show |
4 | HG02818.hp1 HG03139.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-218-102_-218-99de others(5): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214718 | ||||||
| chr7:74214720 | A | T | 13 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(10): Show |
13 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-218-102A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214720 | |||||||
| chr7:74214722 | A | AATATATA others(94): Show |
1 | a0001c0002t0001g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-218-95_-218-94ins others(101): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214722 | ||||||
| chr7:74214722 | A | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218-100A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214722 | |||||||
| chr7:74214724 | T | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-218-98T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214724 | |||||||
| chr7:74214726 | TAA | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0002t0001g0027 |
3 | HG02630.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-218-94_-218-93del others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214726 | ||||||
| chr7:74214727 | A | ATATATGA others(4): Show |
1 | a0001c0001t0001g0034 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-218-95_-218-94ins others(11): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214727 | |||||||
| chr7:74214728 | A | T | 2 | a0001c0002t0001g0026 a0001c0002t0001g0029 |
2 | HG01081.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-218-94A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214728 | |||||||
| chr7:74214730 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0227 a0001c0001t0001g0241 |
3 | HG03139.hp1 NA18983.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-218-92T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214730 | |||||||
| chr7:74214733 | A | G | 1 | a0001c0002t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-218-89A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214733 | |||||||
| chr7:74214734 | T | A | 1 | a0001c0002t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-218-88T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214734 | |||||||
| chr7:74214734 | TATAAAA | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0227 a0001c0001t0001g0241 |
3 | HG03139.hp1 NA18983.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-218-84_-218-79del others(6): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214734 | ||||||
| chr7:74214736 | T | A | 2 | a0001c0002t0001g0026 a0001c0002t0001g0029 |
2 | HG01081.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-218-86T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214736 | |||||||
| chr7:74214737 | A | G | 1 | a0001c0002t0001g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-218-85A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214737 | |||||||
| chr7:74214738 | A | T | 2 | a0001c0002t0001g0026 a0001c0002t0001g0029 |
2 | HG01081.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-218-84A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214738 | |||||||
| chr7:74214738 | AAAATATA others(5): Show |
A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-218-82_-218-71del others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214738 | ||||||
| chr7:74214740 | A | T | 8 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-218-82A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214740 | |||||||
| chr7:74214746 | T | A | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-76T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214746 | |||||||
| chr7:74214748 | A | T | 2 | a0001c0002t0001g0027 a0001c0002t0001g0030 |
2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-218-74A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214748 | |||||||
| chr7:74214748 | AAT | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0038 others(69): Show |
74 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-218-62_-218-61del others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214748 | ||||||
| chr7:74214750 | T | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-218-72T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214750 | |||||||
| chr7:74214750 | T | TATATATA others(17): Show |
1 | a0001c0001t0001g0245 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-218-63_-218-62ins others(24): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214750 | ||||||
| chr7:74214752 | T | A | 1 | a0001c0002t0001g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-218-70T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214752 | |||||||
| chr7:74214756 | T | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218-66T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214756 | |||||||
| chr7:74214758 | T | A | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-64T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214758 | |||||||
| chr7:74214761 | A | G | 3 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0029 |
3 | HG01081.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-218-61A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214761 | |||||||
| chr7:74214762 | A | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218-60A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214762 | |||||||
| chr7:74214764 | C | A | 4 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(1): Show |
4 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-58C>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214764 | |||||||
| chr7:74214764 | C | T | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
7 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218-58C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214764 | |||||||
| chr7:74214766 | T | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218-56T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214766 | |||||||
| chr7:74214768 | T | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-218-54T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214768 | |||||||
| chr7:74214776 | A | AAT | 199 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(196): Show |
216 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.-218-31_-218-30dup others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214776 | ||||||
| chr7:74214776 | A | AATAT | 6 | a0001c0001t0001g0039 a0001c0001t0001g0126 a0001c0001t0001g0127 others(3): Show |
6 | HG00280.hp2 HG01258.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218-33_-218-30dup others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214776 | ||||||
| chr7:74214776 | A | AATATATA others(21): Show |
1 | a0001c0001t0001g0298 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-218-35_-218-34ins others(28): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214776 | ||||||
| chr7:74214776 | A | AATATATA others(23): Show |
1 | a0001c0001t0001g0106 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-218-33_-218-32ins others(30): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214776 | ||||||
| chr7:74214776 | A | T | 2 | a0001c0001t0001g0050 a0001c0002t0001g0030 |
2 | HG00323.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-218-46A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214776 | |||||||
| chr7:74214778 | T | A | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218-44T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214778 | |||||||
| chr7:74214778 | T | C | 1 | a0001c0002t0001g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-218-44T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214778 | |||||||
| chr7:74214780 | T | TATATATA others(118): Show |
1 | a0001c0002t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-218-34_-218-33ins others(125): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214780 | ||||||
| chr7:74214780 | T | TATATATA others(90): Show |
1 | a0001c0002t0001g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-218-34_-218-33ins others(97): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214780 | ||||||
| chr7:74214780 | T | TATATGAA others(114): Show |
1 | a0001c0002t0001g0029 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-218-38_-218-37ins others(121): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214780 | ||||||
| chr7:74214791 | A | ATAT | 23 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(20): Show |
23 | HG00558.hp1 HG00609.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-218-30_-218-29ins others(3): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214791 | ||||||
| chr7:74214791 | A | ATT | 22 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0071 others(19): Show |
23 | HG00597.hp1 HG01928.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.-218-17_-218-16dup others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 74214791 | ||||||
| chr7:74214791 | A | T | 2 | a0001c0001t0001g0018 a0006c0006t0001g0187 |
2 | HG00609.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-218-31A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214791 | |||||||
| chr7:74214792 | T | TA | 13 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
13 | HG01168.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-218-30_-218-29ins others(1): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214792 | |||||||
| chr7:74214792 | T | TATA | 30 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0040 others(27): Show |
31 | HG00280.hp1 HG00597.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-218-30_-218-29ins others(3): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214792 | |||||||
| chr7:74214792 | T | TATATA | 4 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0053 others(1): Show |
5 | HG00621.hp1 NA18945.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-30_-218-29ins others(5): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214792 | |||||||
| chr7:74214793 | T | A | 82 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(79): Show |
84 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.-218-29T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214793 | |||||||
| chr7:74214794 | T | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0229 |
3 | HG01123.hp2 HG02572.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-218-28T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214794 | |||||||
| chr7:74214795 | T | A | 9 | a0001c0001t0001g0231 a0001c0001t0001g0255 a0001c0001t0001g0260 others(6): Show |
9 | HG01074.hp2 HG01081.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-218-27T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214795 | |||||||
| chr7:74214797 | T | A | 1 | a0001c0001t0003g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-218-25T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | chr7 | 74214797 | |||||||
| chr7:74215035 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-30+25T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 2/13 | chr7 | 74215035 | |||||||
| chr7:74215220 | C | T | 1 | a0001c0001t0009g0057 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+210C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 2/13 | chr7 | 74215220 | |||||||
| chr7:74215534 | T | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-413T>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 2/13 | chr7 | 74215534 | |||||||
| chr7:74215660 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-29-287G>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 2/13 | chr7 | 74215660 | |||||||
| chr7:74215682 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-29-265G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 2/13 | chr7 | 74215682 | |||||||
| chr7:74215695 | G | A | 1 | a0001c0005t0001g0130 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-29-252G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 2/13 | chr7 | 74215695 | |||||||
| chr7:74215718 | A | G | 87 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(84): Show |
90 | HG00741.hp2 HG01069.hp1 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.-29-229A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 2/13 | chr7 | 74215718 | |||||||
| chr7:74215825 | G | A | 34 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(31): Show |
35 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-29-122G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 2/13 | chr7 | 74215825 | |||||||
| chr7:74215847 | G | A | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-100G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 2/13 | chr7 | 74215847 | |||||||
| chr7:74215854 | A | G | 12 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(9): Show |
12 | HG01074.hp2 HG01081.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-29-93A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 2/13 | chr7 | 74215854 | |||||||
| chr7:74215872 | G | C | 1 | a0001c0001t0001g0251 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-29-75G>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 2/13 | chr7 | 74215872 | |||||||
| chr7:74216075 | C | T | 1 | a0001c0001t0007g0093 | 1 | HG04199.hp2 | splice_region_variant&intron_variant | LOW | c.94+6C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 3/13 | chr7 | 74216075 | |||||||
| chr7:74216076 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0040 others(13): Show |
17 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(14): Show |
splice_region_variant&intron_variant | LOW | c.94+7G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 3/13 | chr7 | 74216076 | |||||||
| chr7:74216091 | G | A | 4 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(1): Show |
4 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+22G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 3/13 | chr7 | 74216091 | |||||||
| chr7:74216186 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.94+117G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 3/13 | chr7 | 74216186 | |||||||
| chr7:74216195 | G | GA | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+127dupA | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 74216195 | ||||||
| chr7:74216382 | T | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+313T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 3/13 | chr7 | 74216382 | |||||||
| chr7:74216591 | C | T | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02486.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-234C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 3/13 | chr7 | 74216591 | |||||||
| chr7:74216651 | G | A | 13 | a0001c0001t0001g0237 a0001c0001t0001g0246 a0001c0001t0001g0247 others(10): Show |
13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.95-174G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 3/13 | chr7 | 74216651 | |||||||
| chr7:74216758 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0179 |
3 | HG00639.hp2 HG02735.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.95-67G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 3/13 | chr7 | 74216758 | |||||||
| chr7:74217105 | C | T | 1 | a0001c0002t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134+241C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74217105 | |||||||
| chr7:74217189 | T | C | 1 | a0001c0001t0007g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.134+325T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74217189 | |||||||
| chr7:74217292 | G | A | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.134+428G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74217292 | |||||||
| chr7:74217301 | G | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG01069.hp2 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.134+437G>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74217301 | |||||||
| chr7:74217339 | C | G | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.134+475C>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74217339 | |||||||
| chr7:74217358 | G | A | 1 | a0001c0003t0001g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.134+494G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74217358 | |||||||
| chr7:74217478 | C | T | 4 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(1): Show |
4 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.134+614C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74217478 | |||||||
| chr7:74217805 | T | C | 12 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(9): Show |
12 | HG01074.hp2 HG01081.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.134+941T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74217805 | |||||||
| chr7:74217814 | C | T | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.134+950C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74217814 | |||||||
| chr7:74217841 | G | A | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.134+977G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74217841 | |||||||
| chr7:74217899 | A | T | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.134+1035A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74217899 | |||||||
| chr7:74217911 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.134+1047A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74217911 | |||||||
| chr7:74218013 | T | G | 1 | a0001c0001t0001g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.134+1149T>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218013 | |||||||
| chr7:74218073 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.134+1209T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218073 | |||||||
| chr7:74218227 | G | A | 86 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(83): Show |
89 | HG00741.hp2 HG01069.hp1 HG01070.hp1 others(86): Show |
intron_variant | MODIFIER | c.134+1363G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218227 | |||||||
| chr7:74218303 | T | C | 1 | a0001c0001t0003g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.134+1439T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218303 | |||||||
| chr7:74218445 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA18960.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.135-1299A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218445 | |||||||
| chr7:74218457 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.135-1287C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218457 | |||||||
| chr7:74218681 | A | C | 1 | a0001c0001t0001g0226 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.135-1063A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218681 | |||||||
| chr7:74218799 | C | T | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.135-945C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218799 | |||||||
| chr7:74218802 | T | G | 4 | a0001c0001t0001g0103 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG00438.hp1 HG02040.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-942T>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218802 | |||||||
| chr7:74218846 | G | A | 1 | a0001c0002t0001g0029 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.135-898G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218846 | |||||||
| chr7:74218851 | C | G | 1 | a0001c0001t0001g0172 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.135-893C>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218851 | |||||||
| chr7:74218853 | T | C | 4 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(1): Show |
4 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-891T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218853 | |||||||
| chr7:74218863 | A | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.135-881A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218863 | |||||||
| chr7:74218909 | G | A | 1 | a0001c0003t0001g0067 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.135-835G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218909 | |||||||
| chr7:74218964 | C | G | 4 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(1): Show |
4 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-780C>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74218964 | |||||||
| chr7:74219009 | C | CT | 34 | a0001c0001t0001g0032 a0001c0001t0001g0072 a0001c0001t0001g0076 others(31): Show |
35 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.135-697dupT | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | C | CTT | 14 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0035 others(11): Show |
15 | HG01243.hp2 HG01361.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.135-698_135-697dup others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0003g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.135-708_135-697dup others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | CT | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(41): Show |
51 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.135-697delT | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | CTTTTTTT others(3): Show |
C | 30 | a0001c0001t0001g0218 a0001c0001t0001g0229 a0001c0001t0001g0230 others(27): Show |
30 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.135-706_135-697del others(10): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | CTTTTTTT others(4): Show |
C | 55 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(52): Show |
58 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.135-707_135-697del others(11): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0233 a0001c0001t0001g0303 a0001c0001t0001g0304 |
3 | HG01168.hp2 HG03017.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.135-708_135-697del others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.135-710_135-697del others(14): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | CTTTTTTT others(8): Show |
C | 4 | a0001c0001t0001g0105 a0001c0001t0001g0131 a0001c0001t0001g0199 others(1): Show |
4 | HG00639.hp1 HG01109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-711_135-697del others(15): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | CTTTTTTT others(10): Show |
C | 9 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
9 | HG00597.hp2 HG01943.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.135-713_135-697del others(17): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | CTTTTTTT others(11): Show |
C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0038 others(22): Show |
26 | HG00280.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.135-714_135-697del others(18): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0001g0050 a0001c0002t0001g0029 |
2 | HG00323.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.135-715_135-697del others(19): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | CTTTTTTT others(13): Show |
C | 4 | a0001c0001t0001g0226 a0001c0002t0001g0026 a0001c0002t0001g0027 others(1): Show |
4 | HG02630.hp2 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-716_135-697del others(20): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | CTTTTTTT others(16): Show |
C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA18960.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.135-719_135-697del others(23): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219009 | CTTTTTTT others(17): Show |
C | 1 | a0001c0001t0001g0103 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.135-720_135-697del others(24): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 74219009 | ||||||
| chr7:74219043 | T | C | 6 | a0001c0001t0001g0237 a0001c0001t0001g0274 a0001c0001t0001g0279 others(3): Show |
6 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.135-701T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74219043 | |||||||
| chr7:74219069 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0076 |
3 | HG00642.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.135-675G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74219069 | |||||||
| chr7:74219126 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.135-618T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74219126 | |||||||
| chr7:74219364 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135-380C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74219364 | |||||||
| chr7:74219636 | C | T | 9 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.135-108C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74219636 | |||||||
| chr7:74219645 | G | T | 1 | a0001c0001t0001g0300 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.135-99G>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74219645 | |||||||
| chr7:74219727 | A | T | 1 | a0001c0001t0001g0300 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.135-17A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 4/13 | chr7 | 74219727 | |||||||
| chr7:74219861 | A | C | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+74A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 5/13 | chr7 | 74219861 | |||||||
| chr7:74219890 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.179-70G>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 5/13 | chr7 | 74219890 | |||||||
| chr7:74220041 | T | G | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.227+33T>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 6/13 | chr7 | 74220041 | |||||||
| chr7:74220336 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.265+82G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 7/13 | chr7 | 74220336 | |||||||
| chr7:74220432 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.266-152G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 7/13 | chr7 | 74220432 | |||||||
| chr7:74220557 | A | G | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-27A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 7/13 | chr7 | 74220557 | |||||||
| chr7:74220767 | G | GCCTCTCC others(10): Show |
1 | a0001c0002t0001g0029 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.332+71_332+87dupCT others(15): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 74220767 | ||||||
| chr7:74220767 | GCCTCTCC others(10): Show |
G | 9 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(6): Show |
9 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.332+71_332+87delCT others(15): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 74220767 | ||||||
| chr7:74221092 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.332+358C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | chr7 | 74221092 | |||||||
| chr7:74221144 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.332+410G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | chr7 | 74221144 | |||||||
| chr7:74221225 | C | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(138): Show |
146 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.333-412C>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | chr7 | 74221225 | |||||||
| chr7:74221307 | C | A | 1 | a0001c0001t0001g0251 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.333-330C>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | chr7 | 74221307 | |||||||
| chr7:74221307 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.333-330C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | chr7 | 74221307 | |||||||
| chr7:74221330 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.333-307G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | chr7 | 74221330 | |||||||
| chr7:74221410 | C | CA | 80 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(77): Show |
83 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.333-198dupA | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 74221410 | ||||||
| chr7:74221410 | C | CAA | 11 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0058 others(8): Show |
11 | HG00597.hp2 HG00609.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.333-199_333-198dup others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 74221410 | ||||||
| chr7:74221410 | C | CAAA | 6 | a0001c0001t0001g0038 a0001c0001t0001g0046 a0001c0001t0001g0047 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.333-200_333-198dup others(3): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 74221410 | ||||||
| chr7:74221410 | CA | C | 12 | a0001c0001t0001g0023 a0001c0001t0001g0095 a0001c0001t0001g0101 others(9): Show |
13 | HG00642.hp1 HG01069.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.333-198delA | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 74221410 | ||||||
| chr7:74221410 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG02083.hp1 HG02135.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.333-209_333-198del others(12): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 74221410 | ||||||
| chr7:74221617 | GTA | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0053 others(1): Show |
5 | HG00621.hp1 NA18945.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-16_333-15delAT | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 74221617 | ||||||
| chr7:74221699 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0205 a0001c0001t0001g0207 |
3 | NA18951.hp2 NA18962.hp2 NA19090.hp1 |
splice_region_variant&intron_variant | LOW | c.388+7C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74221699 | |||||||
| chr7:74221708 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.388+16A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74221708 | |||||||
| chr7:74221712 | C | CGGT | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
11 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.388+22_388+23insTG others(1): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 74221712 | ||||||
| chr7:74221713 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.388+21G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74221713 | |||||||
| chr7:74221715 | A | C | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
11 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.388+23A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74221715 | |||||||
| chr7:74221718 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.388+26T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74221718 | |||||||
| chr7:74221718 | T | G | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
11 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.388+26T>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74221718 | |||||||
| chr7:74221783 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.388+91T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74221783 | |||||||
| chr7:74221987 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.388+295G>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74221987 | |||||||
| chr7:74222016 | G | C | 1 | a0001c0001t0001g0006 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.388+324G>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74222016 | |||||||
| chr7:74222076 | C | CT | 37 | a0001c0001t0001g0023 a0001c0001t0001g0121 a0001c0001t0001g0191 others(34): Show |
38 | HG01106.hp2 HG01175.hp2 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.388+387dupT | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 74222076 | ||||||
| chr7:74222107 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.388+415C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74222107 | |||||||
| chr7:74222142 | T | C | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+450T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74222142 | |||||||
| chr7:74222167 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.388+475C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74222167 | |||||||
| chr7:74222230 | C | CA | 80 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
83 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.388+559dupA | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 74222230 | ||||||
| chr7:74222230 | CA | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(32): Show |
36 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.388+559delA | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 74222230 | ||||||
| chr7:74222230 | CAAA | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.388+557_388+559del others(3): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 74222230 | ||||||
| chr7:74222243 | A | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.388+551A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74222243 | |||||||
| chr7:74222400 | C | CA | 23 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(20): Show |
23 | HG00639.hp2 HG01074.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.388+722dupA | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 74222400 | ||||||
| chr7:74222582 | A | AT | 6 | a0001c0001t0001g0064 a0001c0001t0001g0078 a0001c0002t0001g0026 others(3): Show |
6 | HG01081.hp2 HG01943.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.388+900dupT | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 74222582 | ||||||
| chr7:74222586 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.388+894T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74222586 | |||||||
| chr7:74222611 | G | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.388+919G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74222611 | |||||||
| chr7:74222654 | A | G | 4 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(1): Show |
4 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+962A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74222654 | |||||||
| chr7:74222698 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(31): Show |
35 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.388+1006C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74222698 | |||||||
| chr7:74222730 | C | T | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-994C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74222730 | |||||||
| chr7:74222992 | T | C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 |
3 | HG01515.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.389-732T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74222992 | |||||||
| chr7:74223001 | T | G | 1 | a0001c0001t0001g0162 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.389-723T>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223001 | |||||||
| chr7:74223009 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.389-715C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223009 | |||||||
| chr7:74223042 | C | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-682C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223042 | |||||||
| chr7:74223050 | G | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0179 |
3 | HG00639.hp2 HG02735.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.389-674G>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223050 | |||||||
| chr7:74223100 | A | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | NA18975.hp2 NA18998.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.389-624A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223100 | |||||||
| chr7:74223104 | A | G | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-620A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223104 | |||||||
| chr7:74223144 | A | G | 12 | a0001c0001t0001g0183 a0001c0001t0001g0218 a0001c0001t0001g0231 others(9): Show |
12 | HG01934.hp2 HG02074.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.389-580A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223144 | |||||||
| chr7:74223147 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0151 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.389-577C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223147 | |||||||
| chr7:74223219 | A | AGAG | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-503_389-501dup others(3): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 74223219 | ||||||
| chr7:74223312 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.389-412G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223312 | |||||||
| chr7:74223453 | C | A | 1 | a0001c0001t0002g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.389-271C>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223453 | |||||||
| chr7:74223579 | A | G | 2 | a0001c0001t0001g0150 a0007c0010t0001g0138 |
2 | NA18995.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.389-145A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223579 | |||||||
| chr7:74223580 | A | C | 2 | a0001c0001t0001g0150 a0007c0010t0001g0138 |
2 | NA18995.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.389-144A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223580 | |||||||
| chr7:74223620 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.389-104C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223620 | |||||||
| chr7:74223621 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0167 a0001c0001t0001g0213 |
3 | HG00642.hp1 HG01106.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.389-103G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223621 | |||||||
| chr7:74223705 | A | G | 25 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0060 others(22): Show |
25 | HG00673.hp1 HG01074.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.389-19A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 10/13 | chr7 | 74223705 | |||||||
| chr7:74223901 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.449-117G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 11/13 | chr7 | 74223901 | |||||||
| chr7:74224403 | T | C | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.628+206T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 12/13 | chr7 | 74224403 | |||||||
| chr7:74224509 | C | T | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.629-130C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 12/13 | chr7 | 74224509 | |||||||
| chr7:74224626 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.629-13C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 12/13 | chr7 | 74224626 | |||||||
| chr7:74224635 | A | G | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.629-4A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 12/13 | chr7 | 74224635 | |||||||
| chr7:74224824 | C | G | 1 | a0001c0001t0001g0007 | 2 | NA18977.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.*18+64C>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74224824 | |||||||
| chr7:74225094 | G | C | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.*18+334G>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74225094 | |||||||
| chr7:74225368 | T | C | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.*18+608T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74225368 | |||||||
| chr7:74225386 | T | G | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.*18+626T>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74225386 | |||||||
| chr7:74225571 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.*18+811C>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74225571 | |||||||
| chr7:74225671 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.*18+911C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74225671 | |||||||
| chr7:74225779 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.*18+1019G>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74225779 | |||||||
| chr7:74225816 | T | C | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
11 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.*18+1056T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74225816 | |||||||
| chr7:74225861 | A | G | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.*18+1101A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74225861 | |||||||
| chr7:74225885 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.*18+1125T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74225885 | |||||||
| chr7:74225914 | C | T | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.*18+1154C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74225914 | |||||||
| chr7:74225949 | C | T | 2 | a0001c0001t0002g0161 a0001c0001t0002g0163 |
2 | HG02451.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.*18+1189C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74225949 | |||||||
| chr7:74226054 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0116 a0001c0001t0001g0165 others(1): Show |
4 | NA18612.hp2 NA18747.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.*18+1294C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74226054 | |||||||
| chr7:74226114 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*18+1354T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74226114 | |||||||
| chr7:74226140 | C | CT | 39 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(36): Show |
40 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.*18+1397dupT | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 74226140 | ||||||
| chr7:74226140 | CT | C | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
11 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.*18+1397delT | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 74226140 | ||||||
| chr7:74226278 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.*18+1518C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74226278 | |||||||
| chr7:74226364 | T | C | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
11 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.*18+1604T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74226364 | |||||||
| chr7:74226785 | C | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0194 |
2 | HG03669.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.*18+2025C>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74226785 | |||||||
| chr7:74226933 | A | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(41): Show |
45 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.*19-2011A>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74226933 | |||||||
| chr7:74227000 | G | C | 2 | a0001c0002t0001g0027 a0001c0002t0001g0028 |
2 | HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*19-1944G>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74227000 | |||||||
| chr7:74227047 | T | G | 2 | a0001c0002t0001g0027 a0001c0002t0001g0028 |
2 | HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*19-1897T>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74227047 | |||||||
| chr7:74227053 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.*19-1891T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74227053 | |||||||
| chr7:74227055 | C | CT | 13 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
13 | HG01243.hp2 HG01891.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.*19-1874dupT | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 74227055 | ||||||
| chr7:74227055 | CT | C | 100 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(97): Show |
104 | HG00741.hp2 HG01069.hp1 HG01070.hp1 others(101): Show |
intron_variant | MODIFIER | c.*19-1874delT | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 74227055 | ||||||
| chr7:74227330 | T | C | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.*19-1614T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74227330 | |||||||
| chr7:74227462 | G | A | 1 | a0001c0001t0003g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.*19-1482G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74227462 | |||||||
| chr7:74227653 | C | A | 1 | a0001c0001t0001g0088 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.*19-1291C>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74227653 | |||||||
| chr7:74227773 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.*19-1171G>A | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74227773 | |||||||
| chr7:74227864 | C | T | 12 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(9): Show |
12 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.*19-1080C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74227864 | |||||||
| chr7:74228123 | C | G | 4 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(1): Show |
4 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.*19-821C>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74228123 | |||||||
| chr7:74228165 | T | TA | 18 | a0001c0001t0001g0038 a0001c0001t0001g0053 a0001c0001t0001g0065 others(15): Show |
18 | HG01255.hp1 HG02056.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.*19-749dupA | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 74228165 | ||||||
| chr7:74228165 | TA | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(144): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.*19-749delA | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 74228165 | ||||||
| chr7:74228165 | TAA | T | 7 | a0001c0001t0001g0134 a0001c0001t0001g0141 a0001c0001t0001g0144 others(4): Show |
7 | HG01496.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.*19-750_*19-749del others(2): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 74228165 | ||||||
| chr7:74228165 | TAAAAAAA others(3): Show |
T | 3 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0030 |
3 | HG02630.hp2 HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*19-758_*19-749del others(10): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 74228165 | ||||||
| chr7:74228165 | TAAAAAAA others(4): Show |
T | 2 | a0001c0002t0001g0026 a0001c0002t0001g0029 |
2 | HG01081.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.*19-759_*19-749del others(11): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 74228165 | ||||||
| chr7:74228165 | TAAAAAAA others(7): Show |
T | 12 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(9): Show |
12 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.*19-762_*19-749del others(14): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 74228165 | ||||||
| chr7:74228328 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.*19-616T>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74228328 | |||||||
| chr7:74228485 | AAAAC | A | 12 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(9): Show |
12 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.*19-447_*19-444del others(4): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 74228485 | ||||||
| chr7:74228523 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18944.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.*19-421C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74228523 | |||||||
| chr7:74228548 | A | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(49): Show |
53 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.*19-396A>G | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74228548 | |||||||
| chr7:74228629 | C | CA | 27 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0044 others(24): Show |
28 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.*19-297dupA | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 74228629 | ||||||
| chr7:74228641 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.*19-303A>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74228641 | |||||||
| chr7:74228705 | C | T | 12 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(9): Show |
12 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.*19-239C>T | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74228705 | |||||||
| chr7:74228900 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.*19-44G>C | LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 13/13 | chr7 | 74228900 |