Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55353 |
| ensemblid | ENSG00000104341.17 |
| hgncid | 13646 |
| symbol | LAPTM4B |
| name | lysosomal protein transmembrane 4 beta |
| refseq_nuc | NM_018407.6 |
| refseq_prot | NP_060877.4 |
| ensembl_nuc | ENST00000521545.7 |
| ensembl_prot | ENSP00000428409.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 97775788 |
| end | 97853013 |
| strand | + |
| ver | v1.2 |
| region | chr8:97775788-97853013 |
| region5000 | chr8:97770788-97858013 |
| regionname0 | LAPTM4B_chr8_97775788_97853013 |
| regionname5000 | LAPTM4B_chr8_97770788_97858013 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 226 | 373 | 94 | 69 | 156 | 14 | 38 | 114 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | MKMVA others(221): Show |
chr8 | 97770788 | 97858013 |
| a0002 | 0/0 | 226 | 6 | 3 | 1 | 0 | 2 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | MKMVA others(221): Show |
chr8 | 97770788 | 97858013 |
| a0003 | 0/0 | 226 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | MKMVA others(221): Show |
chr8 | 97770788 | 97858013 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 678 | 343 | 87 | 54 | 154 | 14 | 32 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | ATGAA others(673): Show |
chr8 | 97770788 | 97858013 | ||
| a0001c0002 | 0/0 | 678 | 25 | 7 | 12 | 0 | 0 | 6 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | ATGAA others(673): Show |
chr8 | 97770788 | 97858013 | ||
| a0001c0004 | 0/0 | 678 | 3 | 0 | 3 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | ATGAA others(673): Show |
chr8 | 97770788 | 97858013 | ||
| a0001c0005 | 0/0 | 678 | 2 | 0 | 0 | 2 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | ATGAA others(673): Show |
chr8 | 97770788 | 97858013 | ||
| a0002c0003 | 0/0 | 678 | 6 | 3 | 1 | 0 | 2 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | ATGAA others(673): Show |
chr8 | 97770788 | 97858013 | ||
| a0003c0006 | 0/0 | 678 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | ATGAA others(673): Show |
chr8 | 97770788 | 97858013 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2442 | 79 | 1 | 14 | 44 | 5 | 15 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2437): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0002 | 0/0 | 2441 | 59 | 20 | 10 | 23 | 2 | 4 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0003 | 0/0 | 2441 | 55 | 13 | 9 | 28 | 1 | 4 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0004 | 1/1 | 2442 | 36 | 0 | 8 | 21 | 1 | 4 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2437): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0005 | 0/0 | 2441 | 29 | 12 | 2 | 14 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0006 | 0/0 | 2441 | 13 | 13 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0007 | 0/0 | 2441 | 12 | 2 | 4 | 6 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0008 | 0/0 | 2441 | 11 | 11 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0010 | 0/0 | 2441 | 9 | 3 | 1 | 5 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0011 | 0/0 | 2441 | 7 | 0 | 4 | 0 | 2 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0012 | 0/0 | 2441 | 4 | 0 | 0 | 3 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0013 | 0/0 | 2441 | 3 | 1 | 0 | 2 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0014 | 0/0 | 2443 | 5 | 1 | 2 | 0 | 2 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2438): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0016 | 0/0 | 2441 | 4 | 0 | 0 | 4 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0022 | 0/0 | 2442 | 2 | 1 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2437): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0023 | 0/0 | 2441 | 2 | 0 | 0 | 0 | 1 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0024 | 0/0 | 2441 | 2 | 0 | 0 | 2 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0025 | 0/0 | 2442 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2437): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0027 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2437): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0028 | 0/0 | 2441 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0029 | 0/0 | 2441 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0030 | 0/0 | 2441 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0031 | 0/0 | 2441 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0032 | 0/0 | 2441 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0033 | 0/0 | 2441 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0034 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2438): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0035 | 0/0 | 2441 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0001t0036 | 0/0 | 2441 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0002t0009 | 0/0 | 2457 | 9 | 3 | 3 | 0 | 0 | 3 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2452): Show |
chr8 | 97770788 | 97858013 |
| a0001c0002t0015 | 0/0 | 2458 | 4 | 0 | 2 | 0 | 0 | 2 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2453): Show |
chr8 | 97770788 | 97858013 |
| a0001c0002t0017 | 0/0 | 2457 | 3 | 2 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2452): Show |
chr8 | 97770788 | 97858013 |
| a0001c0002t0018 | 0/0 | 2457 | 2 | 2 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2452): Show |
chr8 | 97770788 | 97858013 |
| a0001c0002t0019 | 0/0 | 2457 | 2 | 0 | 2 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2452): Show |
chr8 | 97770788 | 97858013 |
| a0001c0002t0020 | 0/0 | 2457 | 2 | 0 | 2 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2452): Show |
chr8 | 97770788 | 97858013 |
| a0001c0002t0021 | 0/0 | 2458 | 2 | 0 | 2 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2453): Show |
chr8 | 97770788 | 97858013 |
| a0001c0002t0026 | 0/0 | 2459 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2454): Show |
chr8 | 97770788 | 97858013 |
| a0001c0004t0004 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2437): Show |
chr8 | 97770788 | 97858013 |
| a0001c0004t0012 | 0/0 | 2441 | 2 | 0 | 2 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0001c0005t0001 | 0/0 | 2442 | 2 | 0 | 0 | 2 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2437): Show |
chr8 | 97770788 | 97858013 |
| a0002c0003t0005 | 0/0 | 2441 | 3 | 2 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0002c0003t0013 | 0/0 | 2441 | 3 | 1 | 0 | 0 | 2 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| a0003c0006t0005 | 0/0 | 2441 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | GTCCC others(2436): Show |
chr8 | 97770788 | 97858013 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0002g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0003g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0005g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0006g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0007g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0007g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0007g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0008g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0010g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0010g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0010g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0010g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0010g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0010g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0010g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0010g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0011g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0011g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0011g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0011g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0011g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0011g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0011g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0012g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0012g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0012g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0012g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0013g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0013g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0014g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0014g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0014g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0014g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0014g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0016g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0016g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0016g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0016g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0022g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0022g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0023g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0023g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0024g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0024g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0025g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0027g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0028g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0029g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0030g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0031g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0032g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0033g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0034g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0035g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0001t0036g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0009g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0009g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0009g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0009g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0009g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0009g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0009g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0015g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0015g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0015g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0015g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0017g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0017g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0017g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0018g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0018g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0019g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0019g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0020g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0020g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0021g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0021g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0002t0026g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0004t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0004t0012g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0004t0012g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0005t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0001c0005t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0002c0003t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0002c0003t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0002c0003t0005g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0002c0003t0013g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0002c0003t0013g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0002c0003t0013g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| a0003c0006t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0191 | EUR | GBR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0295 | EUR | GBR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0350 | EUR | GBR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | GBR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00280 | hp1 | a0001 | c0001 | t0011 | g0057 | EUR | FIN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00280 | hp2 | a0001 | c0001 | t0023 | g0220 | EUR | FIN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0260 | EUR | FIN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00323 | hp2 | a0001 | c0001 | t0014 | g0172 | EUR | FIN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00423 | hp2 | a0001 | c0001 | t0016 | g0339 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00438 | hp1 | a0001 | c0001 | t0010 | g0226 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00438 | hp2 | a0001 | c0001 | t0016 | g0352 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00558 | hp1 | a0001 | c0005 | t0001 | g0016 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00609 | hp2 | a0001 | c0001 | t0010 | g0194 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0179 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0297 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0160 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00673 | hp2 | a0001 | c0001 | t0012 | g0129 | EAS | CHS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0036 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00733 | hp2 | a0001 | c0002 | t0009 | g0250 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00735 | hp2 | a0001 | c0002 | t0021 | g0241 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00738 | hp1 | a0001 | c0001 | t0011 | g0109 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0046 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00741 | hp1 | a0001 | c0002 | t0015 | g0245 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG00741 | hp2 | a0001 | c0002 | t0009 | g0380 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0183 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01081 | hp1 | a0001 | c0001 | t0011 | g0280 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0360 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01099 | hp1 | a0001 | c0002 | t0009 | g0378 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0338 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01106 | hp1 | a0001 | c0001 | t0014 | g0205 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01167 | hp1 | a0002 | c0003 | t0005 | g0083 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0195 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01168 | hp1 | a0001 | c0002 | t0026 | g0243 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01168 | hp2 | a0001 | c0002 | t0020 | g0376 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01169 | hp1 | a0001 | c0002 | t0020 | g0379 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0228 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0345 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0227 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01243 | hp1 | a0001 | c0002 | t0015 | g0247 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0370 | AMR | PUR | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0336 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0222 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01358 | hp1 | a0001 | c0001 | t0011 | g0282 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0173 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01361 | hp1 | a0001 | c0002 | t0019 | g0246 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01361 | hp2 | a0001 | c0001 | t0014 | g0207 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01433 | hp2 | a0001 | c0001 | t0011 | g0349 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01496 | hp1 | a0001 | c0002 | t0019 | g0164 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0069 | EUR | IBS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01515 | hp2 | a0002 | c0003 | t0013 | g0216 | EUR | IBS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01517 | hp1 | a0002 | c0003 | t0013 | g0190 | EUR | IBS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0300 | EUR | IBS | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01884 | hp2 | a0001 | c0002 | t0009 | g0166 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0230 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0189 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01952 | hp1 | a0001 | c0004 | t0012 | g0237 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0296 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01975 | hp1 | a0001 | c0004 | t0004 | g0217 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0347 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0203 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0223 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01993 | hp2 | a0001 | c0004 | t0012 | g0218 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02004 | hp1 | a0001 | c0002 | t0021 | g0244 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02015 | hp2 | a0001 | c0001 | t0007 | g0211 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0255 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02055 | hp2 | a0002 | c0003 | t0005 | g0126 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0334 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02056 | hp2 | a0001 | c0005 | t0001 | g0023 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0335 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0341 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0152 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02083 | hp1 | a0001 | c0001 | t0005 | g0045 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0135 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0119 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02258 | hp1 | a0001 | c0001 | t0028 | g0363 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0053 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PEL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0174 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02451 | hp2 | a0001 | c0001 | t0031 | g0030 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02572 | hp2 | a0001 | c0001 | t0022 | g0048 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02615 | hp1 | a0001 | c0002 | t0009 | g0251 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0372 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0011 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02622 | hp2 | a0002 | c0003 | t0013 | g0215 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02630 | hp1 | a0001 | c0001 | t0035 | g0204 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0039 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0082 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02717 | hp1 | a0001 | c0001 | t0029 | g0374 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02723 | hp2 | a0001 | c0001 | t0030 | g0065 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0187 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0371 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02818 | hp1 | a0002 | c0003 | t0005 | g0351 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0358 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0253 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0127 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02895 | hp1 | a0001 | c0002 | t0017 | g0239 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0308 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02897 | hp1 | a0001 | c0002 | t0017 | g0238 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0080 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0020 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0198 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0369 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0332 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03130 | hp1 | a0001 | c0002 | t0018 | g0242 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0019 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0366 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03195 | hp2 | a0001 | c0001 | t0033 | g0047 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03209 | hp1 | a0001 | c0002 | t0018 | g0165 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0161 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0278 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03486 | hp1 | a0001 | c0001 | t0027 | g0302 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0361 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03491 | hp1 | a0001 | c0002 | t0017 | g0240 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0346 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03516 | hp1 | a0001 | c0001 | t0013 | g0113 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0118 | AFR | ESN | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0359 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0171 | AFR | GWD | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03654 | hp1 | a0001 | c0001 | t0023 | g0209 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0163 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0344 | SAS | STU | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03688 | hp2 | a0001 | c0002 | t0015 | g0167 | SAS | STU | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03704 | hp2 | a0001 | c0002 | t0009 | g0248 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03710 | hp1 | a0001 | c0002 | t0009 | g0377 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03710 | hp2 | a0001 | c0001 | t0011 | g0033 | SAS | PJL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0213 | SAS | BEB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | BEB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0058 | SAS | BEB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03942 | hp1 | a0001 | c0002 | t0009 | g0168 | SAS | BEB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0348 | SAS | BEB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0303 | SAS | BEB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0199 | SAS | BEB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG04199 | hp1 | a0001 | c0001 | t0025 | g0292 | SAS | STU | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | STU | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | STU | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0326 | SAS | STU | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG04228 | hp1 | a0001 | c0001 | t0012 | g0193 | SAS | STU | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | YRI | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18522 | hp2 | a0003 | c0006 | t0005 | g0034 | AFR | YRI | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | CHB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | CHB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CHB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | CHB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | YRI | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0368 | AFR | YRI | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18940 | hp2 | a0001 | c0001 | t0032 | g0318 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18941 | hp2 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18947 | hp2 | a0001 | c0001 | t0013 | g0235 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0321 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18957 | hp2 | a0001 | c0001 | t0007 | g0178 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18959 | hp2 | a0001 | c0001 | t0024 | g0200 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18960 | hp1 | a0001 | c0001 | t0010 | g0185 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18964 | hp1 | a0001 | c0001 | t0016 | g0134 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18974 | hp1 | a0001 | c0001 | t0013 | g0234 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18982 | hp1 | a0001 | c0001 | t0007 | g0182 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18983 | hp2 | a0001 | c0001 | t0007 | g0188 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0158 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19005 | hp1 | a0001 | c0001 | t0024 | g0201 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0343 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19010 | hp2 | a0001 | c0001 | t0010 | g0180 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | LWK | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0373 | AFR | LWK | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0170 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19054 | hp2 | a0001 | c0001 | t0012 | g0357 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0131 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19060 | hp1 | a0001 | c0001 | t0010 | g0202 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19065 | hp1 | a0001 | c0001 | t0016 | g0276 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19067 | hp2 | a0001 | c0001 | t0022 | g0132 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19090 | hp2 | a0001 | c0001 | t0012 | g0130 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0252 | AFR | YRI | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0041 | AFR | YRI | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | ASW | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA20129 | hp2 | a0001 | c0002 | t0009 | g0375 | AFR | ASW | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA20752 | hp1 | a0001 | c0001 | t0011 | g0072 | EUR | TSI | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0261 | EUR | TSI | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA20805 | hp2 | a0001 | c0001 | t0014 | g0206 | EUR | TSI | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA20905 | hp1 | a0001 | c0002 | t0015 | g0249 | SAS | GIH | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0309 | AMR | CLM | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0027 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0367 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0364 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | ACB | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03471 | hp1 | a0001 | c0001 | t0036 | g0122 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0365 | AFR | MSL | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG06807 | hp1 | a0001 | c0001 | t0034 | g0254 | AFR | USA | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0362 | AFR | USA | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | USA | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA20300 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | USA | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | LWK | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0214 | REF | REF | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0176 | REF | REF | LAPTM4B_chr8_97770788_97858013 | LAPTM4B | chr8 | 97770788 | 97858013 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:97805407 | C | G | 1 | a0003 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.154C>G | p.Gln52Glu | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/7 | 376/2442 | 154/681 | 52/226 | chr8 | 97805407 | |||
| chr8:97851449 | C | T | 1 | a0002 | 6 | HG01167.hp1 HG01515.hp2 HG01517.hp1 others(3): Show |
missense_variant | MODERATE | c.656C>T | p.Pro219Leu | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 878/2442 | 656/681 | 219/226 | chr8 | 97851449 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:97776033 | G | T | 1 | a0001c0002 | 25 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
synonymous_variant | LOW | c.24G>T | p.Thr8Thr | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/7 | 246/2442 | 24/681 | 8/226 | chr8 | 97776033 | |||
| chr8:97776093 | C | A | 1 | a0001c0004 | 3 | HG01952.hp1 HG01975.hp1 HG01993.hp2 |
synonymous_variant | LOW | c.84C>A | p.Leu28Leu | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/7 | 306/2442 | 84/681 | 28/226 | chr8 | 97776093 | |||
| chr8:97851411 | G | T | 1 | a0001c0005 | 2 | HG00558.hp1 HG02056.hp2 |
synonymous_variant | LOW | c.618G>T | p.Pro206Pro | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 840/2442 | 618/681 | 206/226 | chr8 | 97851411 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:97775805 | G | C | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(26): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
5_prime_UTR_variant | MODIFIER | c.-205G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/7 | 205 | chr8 | 97775805 | ||||||
| chr8:97775937 | C | CGGCGGGC others(9): Show |
8 | a0001c0002t0009 a0001c0002t0015 a0001c0002t0017 others(5): Show |
25 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-67_-52dupGCTCCAGG others(8): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/7 | 51 | INFO_REALIGN_3_PRIME | chr8 | 97775937 | |||||
| chr8:97775951 | C | A | 1 | a0001c0001t0025 | 1 | HG04199.hp1 | 5_prime_UTR_variant | MODIFIER | c.-59C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/7 | 59 | chr8 | 97775951 | ||||||
| chr8:97851648 | G | A | 33 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(30): Show |
250 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*174G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 174 | chr8 | 97851648 | ||||||
| chr8:97851672 | A | G | 1 | a0001c0001t0036 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*198A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 198 | chr8 | 97851672 | ||||||
| chr8:97851687 | C | A | 5 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0027 others(2): Show |
28 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*213C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 213 | chr8 | 97851687 | ||||||
| chr8:97851702 | T | C | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(23): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*228T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 228 | chr8 | 97851702 | ||||||
| chr8:97851874 | G | T | 16 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(13): Show |
115 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*400G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 400 | chr8 | 97851874 | ||||||
| chr8:97851903 | G | C | 1 | a0001c0001t0034 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*429G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 429 | chr8 | 97851903 | ||||||
| chr8:97851911 | A | G | 1 | a0001c0001t0032 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*437A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 437 | chr8 | 97851911 | ||||||
| chr8:97852095 | G | A | 3 | a0001c0001t0011 a0001c0001t0023 a0001c0002t0019 |
11 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*621G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 621 | chr8 | 97852095 | ||||||
| chr8:97852280 | C | T | 1 | a0001c0001t0024 | 2 | NA18959.hp2 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*806C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 806 | chr8 | 97852280 | ||||||
| chr8:97852283 | A | T | 3 | a0001c0001t0012 a0001c0001t0016 a0001c0004t0012 |
10 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*809A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 809 | chr8 | 97852283 | ||||||
| chr8:97852288 | C | CT | 3 | a0001c0001t0014 a0001c0001t0034 a0001c0002t0026 |
7 | HG00323.hp2 HG01106.hp1 HG01168.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*817dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 818 | INFO_REALIGN_3_PRIME | chr8 | 97852288 | |||||
| chr8:97852289 | T | A | 1 | a0001c0002t0020 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*815T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 815 | chr8 | 97852289 | ||||||
| chr8:97852505 | A | G | 1 | a0001c0001t0031 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1031A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 1031 | chr8 | 97852505 | ||||||
| chr8:97852566 | T | C | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(22): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*1092T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 1092 | chr8 | 97852566 | ||||||
| chr8:97852693 | CT | C | 11 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(8): Show |
110 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1227delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 1227 | INFO_REALIGN_3_PRIME | chr8 | 97852693 | |||||
| chr8:97852701 | T | G | 1 | a0001c0001t0027 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1227T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 1227 | chr8 | 97852701 | ||||||
| chr8:97852701 | TG | T | 19 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(16): Show |
135 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1236delG | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 1236 | INFO_REALIGN_3_PRIME | chr8 | 97852701 | |||||
| chr8:97852703 | G | C | 1 | a0001c0001t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1229G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 1229 | chr8 | 97852703 | ||||||
| chr8:97852703 | G | T | 1 | a0001c0001t0008 | 11 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1229G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 1229 | chr8 | 97852703 | ||||||
| chr8:97852705 | G | T | 3 | a0001c0001t0012 a0001c0001t0016 a0001c0004t0012 |
10 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1231G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 1231 | chr8 | 97852705 | ||||||
| chr8:97852795 | A | G | 1 | a0001c0001t0029 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1321A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 1321 | chr8 | 97852795 | ||||||
| chr8:97852905 | G | C | 1 | a0001c0001t0033 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1431G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 7/7 | 1431 | chr8 | 97852905 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:97776258 | C | T | 6 | a0001c0002t0009g0375 a0001c0002t0009g0377 a0001c0002t0009g0378 others(3): Show |
6 | HG00741.hp2 HG01099.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+150C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776258 | |||||||
| chr8:97776267 | G | A | 1 | a0001c0001t0003g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+159G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776267 | |||||||
| chr8:97776283 | CTGGGGGA others(19): Show |
C | 4 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+190_99+215delAG others(24): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97776283 | ||||||
| chr8:97776305 | G | C | 1 | a0001c0001t0005g0255 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.99+197G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776305 | |||||||
| chr8:97776375 | C | G | 1 | a0001c0001t0007g0370 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.99+267C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776375 | |||||||
| chr8:97776380 | A | C | 12 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(9): Show |
12 | HG01081.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+272A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776380 | |||||||
| chr8:97776420 | G | T | 1 | a0001c0001t0012g0357 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.99+312G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776420 | |||||||
| chr8:97776465 | C | T | 4 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+357C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776465 | |||||||
| chr8:97776560 | G | C | 10 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0005g0006 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+452G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776560 | |||||||
| chr8:97776670 | G | A | 1 | a0001c0001t0004g0012 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.99+562G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776670 | |||||||
| chr8:97776690 | T | TC | 106 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(103): Show |
106 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.99+591dupC | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97776690 | ||||||
| chr8:97776690 | T | TCC | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(15): Show |
18 | HG00558.hp1 HG00621.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+590_99+591dupCC | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97776690 | ||||||
| chr8:97776700 | G | C | 4 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+592G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776700 | |||||||
| chr8:97776764 | G | T | 1 | a0001c0001t0006g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.99+656G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776764 | |||||||
| chr8:97776870 | G | A | 4 | a0001c0001t0007g0031 a0001c0001t0012g0129 a0001c0001t0012g0130 others(1): Show |
4 | HG00673.hp2 NA18941.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+762G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776870 | |||||||
| chr8:97776871 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.99+763A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776871 | |||||||
| chr8:97776886 | T | G | 32 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0001g0146 others(29): Show |
32 | HG00673.hp1 HG01884.hp1 HG02027.hp2 others(29): Show |
intron_variant | MODIFIER | c.99+778T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776886 | |||||||
| chr8:97776913 | G | C | 1 | a0001c0001t0005g0131 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.99+805G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776913 | |||||||
| chr8:97776934 | G | A | 1 | a0001c0001t0011g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.99+826G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776934 | |||||||
| chr8:97776945 | C | G | 2 | a0001c0001t0006g0127 a0002c0003t0005g0126 |
2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.99+837C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776945 | |||||||
| chr8:97776945 | C | T | 104 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0263 others(101): Show |
104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.99+837C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776945 | |||||||
| chr8:97776971 | C | T | 4 | a0001c0001t0007g0031 a0001c0001t0012g0129 a0001c0001t0012g0130 others(1): Show |
4 | HG00673.hp2 NA18941.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+863C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97776971 | |||||||
| chr8:97777099 | A | G | 2 | a0001c0001t0010g0252 a0001c0001t0010g0253 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.99+991A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97777099 | |||||||
| chr8:97777119 | A | G | 32 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0001g0146 others(29): Show |
32 | HG00673.hp1 HG01884.hp1 HG02027.hp2 others(29): Show |
intron_variant | MODIFIER | c.99+1011A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97777119 | |||||||
| chr8:97777137 | G | GT | 118 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0153 others(115): Show |
118 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.99+1056dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97777137 | ||||||
| chr8:97777137 | G | GTT | 19 | a0001c0001t0001g0355 a0001c0001t0002g0156 a0001c0001t0003g0032 others(16): Show |
19 | HG00673.hp1 HG01952.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+1055_99+1056dup others(2): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97777137 | ||||||
| chr8:97777137 | G | GTTTTTTT others(1): Show |
13 | a0001c0001t0002g0003 a0001c0001t0006g0004 a0001c0001t0006g0005 others(10): Show |
13 | HG00735.hp2 HG00741.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+1049_99+1056dup others(8): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97777137 | ||||||
| chr8:97777137 | G | GTTTTTTT others(2): Show |
8 | a0001c0001t0005g0006 a0001c0001t0006g0007 a0001c0002t0015g0245 others(5): Show |
8 | HG00741.hp1 HG01168.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+1048_99+1056dup others(9): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97777137 | ||||||
| chr8:97777137 | G | GTTTTTTT others(3): Show |
1 | a0001c0002t0009g0248 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.99+1047_99+1056dup others(10): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97777137 | ||||||
| chr8:97777137 | G | GTTTTTTT others(4): Show |
3 | a0001c0002t0009g0250 a0001c0002t0009g0251 a0001c0002t0015g0249 |
3 | HG00733.hp2 HG02615.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.99+1046_99+1056dup others(11): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97777137 | ||||||
| chr8:97777137 | GT | G | 41 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(38): Show |
41 | HG00280.hp1 HG00558.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.99+1056delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97777137 | ||||||
| chr8:97777137 | GTT | G | 11 | a0001c0001t0003g0013 a0001c0001t0003g0050 a0001c0001t0003g0371 others(8): Show |
11 | HG00738.hp2 HG02083.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+1055_99+1056del others(2): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97777137 | ||||||
| chr8:97777137 | GTTT | G | 11 | a0001c0001t0002g0038 a0001c0001t0002g0042 a0001c0001t0003g0040 others(8): Show |
11 | HG00733.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+1054_99+1056del others(3): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97777137 | ||||||
| chr8:97777145 | T | G | 6 | a0001c0001t0002g0360 a0001c0001t0002g0364 a0001c0001t0005g0361 others(3): Show |
6 | HG01081.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+1037T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97777145 | |||||||
| chr8:97777146 | T | G | 2 | a0001c0001t0002g0358 a0001c0001t0002g0359 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.99+1038T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97777146 | |||||||
| chr8:97777306 | C | T | 1 | a0001c0001t0006g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99+1198C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97777306 | |||||||
| chr8:97777589 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.99+1481C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97777589 | |||||||
| chr8:97777662 | T | C | 1 | a0001c0001t0004g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.99+1554T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97777662 | |||||||
| chr8:97777939 | A | G | 5 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+1831A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97777939 | |||||||
| chr8:97778049 | A | G | 1 | a0001c0001t0001g0353 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.99+1941A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97778049 | |||||||
| chr8:97778108 | T | C | 1 | a0001c0001t0027g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.99+2000T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97778108 | |||||||
| chr8:97778188 | A | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0115 others(6): Show |
9 | HG01175.hp2 HG02896.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+2080A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97778188 | |||||||
| chr8:97778747 | C | T | 2 | a0001c0001t0008g0028 a0001c0001t0008g0029 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.99+2639C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97778747 | |||||||
| chr8:97778790 | T | C | 98 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0001g0146 others(95): Show |
98 | HG00673.hp1 HG00733.hp2 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.99+2682T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97778790 | |||||||
| chr8:97778878 | A | G | 1 | a0001c0001t0003g0114 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.99+2770A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97778878 | |||||||
| chr8:97778937 | T | A | 4 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+2829T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97778937 | |||||||
| chr8:97779221 | T | A | 1 | a0001c0001t0004g0169 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.99+3113T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97779221 | |||||||
| chr8:97779252 | G | A | 1 | a0001c0001t0003g0257 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.99+3144G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97779252 | |||||||
| chr8:97779402 | T | A | 1 | a0001c0001t0004g0199 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.99+3294T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97779402 | |||||||
| chr8:97779468 | G | A | 4 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+3360G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97779468 | |||||||
| chr8:97779584 | A | C | 1 | a0001c0001t0016g0352 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.99+3476A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97779584 | |||||||
| chr8:97779597 | C | CAACAT | 106 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0263 others(103): Show |
106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.99+3490_99+3494dup others(5): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97779597 | ||||||
| chr8:97779614 | G | A | 94 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(91): Show |
94 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.99+3506G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97779614 | |||||||
| chr8:97779712 | G | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.99+3604G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97779712 | |||||||
| chr8:97779753 | T | TA | 11 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0003g0076 others(8): Show |
11 | HG01978.hp2 HG02293.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+3663dupA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97779753 | ||||||
| chr8:97779820 | G | A | 8 | a0001c0001t0002g0009 a0001c0001t0007g0031 a0001c0001t0007g0171 others(5): Show |
8 | HG00673.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+3712G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97779820 | |||||||
| chr8:97779986 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.99+3878G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97779986 | |||||||
| chr8:97779992 | C | T | 1 | a0001c0001t0027g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.99+3884C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97779992 | |||||||
| chr8:97780042 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.99+3934C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780042 | |||||||
| chr8:97780050 | C | CA | 7 | a0001c0001t0001g0051 a0001c0001t0001g0087 a0001c0001t0002g0003 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+3960dupA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97780050 | ||||||
| chr8:97780050 | CA | C | 253 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0001g0146 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.99+3960delA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97780050 | ||||||
| chr8:97780050 | CAA | C | 10 | a0001c0001t0002g0301 a0001c0001t0004g0169 a0001c0001t0006g0127 others(7): Show |
10 | HG00673.hp2 HG02055.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+3959_99+3960del others(2): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97780050 | ||||||
| chr8:97780146 | C | T | 1 | a0001c0001t0036g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99+4038C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780146 | |||||||
| chr8:97780154 | G | A | 4 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+4046G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780154 | |||||||
| chr8:97780254 | T | C | 307 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(304): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.99+4146T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780254 | |||||||
| chr8:97780297 | C | T | 17 | a0001c0001t0002g0038 a0001c0001t0002g0042 a0001c0001t0003g0013 others(14): Show |
17 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+4189C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780297 | |||||||
| chr8:97780406 | C | G | 94 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(91): Show |
94 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.99+4298C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780406 | |||||||
| chr8:97780417 | C | A | 8 | a0001c0001t0002g0009 a0001c0001t0007g0031 a0001c0001t0007g0171 others(5): Show |
8 | HG00673.hp2 HG02630.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+4309C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780417 | |||||||
| chr8:97780458 | A | C | 24 | a0001c0002t0009g0166 a0001c0002t0009g0168 a0001c0002t0009g0248 others(21): Show |
24 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.99+4350A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780458 | |||||||
| chr8:97780496 | T | A | 1 | a0001c0001t0003g0114 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.99+4388T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780496 | |||||||
| chr8:97780517 | C | A | 4 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+4409C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780517 | |||||||
| chr8:97780549 | A | G | 2 | a0001c0001t0007g0198 a0001c0001t0013g0113 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+4441A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780549 | |||||||
| chr8:97780595 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | NA19000.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.99+4487T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780595 | |||||||
| chr8:97780597 | C | G | 94 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(91): Show |
94 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.99+4489C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780597 | |||||||
| chr8:97780685 | C | G | 14 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(11): Show |
14 | HG01081.hp2 HG02258.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+4577C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780685 | |||||||
| chr8:97780712 | A | T | 1 | a0001c0001t0004g0169 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.99+4604A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780712 | |||||||
| chr8:97780905 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.99+4797A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780905 | |||||||
| chr8:97780926 | T | G | 17 | a0001c0001t0002g0081 a0001c0001t0003g0084 a0001c0001t0005g0025 others(14): Show |
17 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.99+4818T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780926 | |||||||
| chr8:97780938 | T | C | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.99+4830T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780938 | |||||||
| chr8:97780985 | A | G | 2 | a0001c0002t0017g0238 a0001c0002t0017g0239 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.99+4877A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780985 | |||||||
| chr8:97780993 | C | T | 16 | a0001c0001t0001g0070 a0001c0001t0001g0087 a0001c0001t0001g0108 others(13): Show |
16 | HG00642.hp2 HG00738.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+4885C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97780993 | |||||||
| chr8:97780995 | A | AT | 7 | a0001c0001t0001g0107 a0001c0001t0003g0084 a0001c0001t0003g0371 others(4): Show |
7 | HG02027.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+4899dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97780995 | ||||||
| chr8:97780995 | AT | A | 17 | a0001c0001t0001g0070 a0001c0001t0001g0087 a0001c0001t0001g0108 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.99+4899delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97780995 | ||||||
| chr8:97781093 | G | A | 1 | a0001c0001t0027g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.99+4985G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97781093 | |||||||
| chr8:97781168 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.99+5060A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97781168 | |||||||
| chr8:97781212 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.99+5104C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97781212 | |||||||
| chr8:97781258 | C | T | 4 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+5150C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97781258 | |||||||
| chr8:97781275 | G | A | 1 | a0001c0001t0002g0305 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.99+5167G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97781275 | |||||||
| chr8:97781278 | C | CT | 9 | a0001c0001t0004g0123 a0001c0001t0004g0177 a0001c0001t0004g0196 others(6): Show |
9 | HG01175.hp1 HG01891.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+5191dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTT | 34 | a0001c0001t0001g0070 a0001c0001t0001g0087 a0001c0001t0001g0108 others(31): Show |
34 | HG00642.hp2 HG00738.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.99+5189_99+5191dup others(3): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTT | 48 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0052 others(45): Show |
48 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.99+5188_99+5191dup others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTTT | 37 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0024 others(34): Show |
37 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.99+5187_99+5191dup others(5): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTTTT | 36 | a0001c0001t0001g0105 a0001c0001t0001g0306 a0001c0001t0001g0307 others(33): Show |
36 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.99+5186_99+5191dup others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTTTTT | 77 | a0001c0001t0001g0256 a0001c0001t0001g0263 a0001c0001t0001g0264 others(74): Show |
77 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.99+5185_99+5191dup others(7): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTTTTT others(1): Show |
52 | a0001c0001t0001g0133 a0001c0001t0001g0153 a0001c0001t0001g0291 others(49): Show |
52 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.99+5184_99+5191dup others(8): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTTTTT others(2): Show |
7 | a0001c0001t0001g0300 a0001c0001t0001g0350 a0001c0001t0007g0031 others(4): Show |
7 | HG00140.hp1 HG00673.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+5183_99+5191dup others(9): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0008g0027 a0001c0001t0012g0130 |
2 | HG02109.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.99+5182_99+5191dup others(10): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0002g0003 a0001c0001t0005g0006 |
2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.99+5179_99+5191dup others(13): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0006g0002 a0001c0001t0007g0171 |
2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.99+5177_99+5191dup others(15): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.99+5176_99+5191dup others(16): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0036g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99+5175_99+5191dup others(17): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0006g0004 a0001c0001t0027g0302 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.99+5174_99+5191dup others(18): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTTTTT others(12): Show |
2 | a0001c0001t0002g0009 a0001c0001t0006g0005 |
2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.99+5173_99+5191dup others(19): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781278 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0006g0007 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.99+5191_99+5192ins others(22): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781278 | ||||||
| chr8:97781344 | A | G | 17 | a0001c0001t0001g0070 a0001c0001t0001g0087 a0001c0001t0001g0108 others(14): Show |
17 | HG00642.hp2 HG00738.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.99+5236A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97781344 | |||||||
| chr8:97781802 | C | G | 1 | a0001c0001t0002g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99+5694C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97781802 | |||||||
| chr8:97781828 | G | A | 5 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0086 others(2): Show |
5 | HG01943.hp2 HG01975.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+5720G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97781828 | |||||||
| chr8:97781864 | A | G | 14 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(11): Show |
14 | HG01081.hp2 HG02258.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+5756A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97781864 | |||||||
| chr8:97781981 | CT | C | 197 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0070 others(194): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.99+5889delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781981 | ||||||
| chr8:97781981 | CTTTTTT | C | 23 | a0001c0002t0009g0166 a0001c0002t0009g0168 a0001c0002t0009g0248 others(20): Show |
23 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.99+5884_99+5889del others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97781981 | ||||||
| chr8:97782003 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0106 |
2 | NA18953.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.99+5895A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782003 | |||||||
| chr8:97782038 | T | C | 17 | a0001c0001t0002g0038 a0001c0001t0002g0042 a0001c0001t0003g0013 others(14): Show |
17 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+5930T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782038 | |||||||
| chr8:97782091 | C | T | 1 | a0001c0001t0006g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.99+5983C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782091 | |||||||
| chr8:97782182 | T | C | 2 | a0001c0001t0007g0198 a0001c0001t0013g0113 |
2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+6074T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782182 | |||||||
| chr8:97782201 | G | A | 1 | a0001c0001t0003g0285 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.99+6093G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782201 | |||||||
| chr8:97782274 | C | T | 19 | a0001c0001t0002g0081 a0001c0001t0002g0139 a0001c0001t0003g0084 others(16): Show |
19 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+6166C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782274 | |||||||
| chr8:97782279 | C | CT | 120 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0051 others(117): Show |
120 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.99+6198dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782279 | ||||||
| chr8:97782279 | C | CTT | 98 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0024 others(95): Show |
98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.99+6197_99+6198dup others(2): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782279 | ||||||
| chr8:97782279 | C | CTTT | 33 | a0001c0001t0001g0068 a0001c0001t0001g0106 a0001c0001t0001g0111 others(30): Show |
33 | HG00140.hp1 HG00738.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.99+6196_99+6198dup others(3): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782279 | ||||||
| chr8:97782279 | C | CTTTT | 7 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0076 others(4): Show |
7 | HG01123.hp2 HG02280.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+6195_99+6198dup others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782279 | ||||||
| chr8:97782279 | C | CTTTTT | 10 | a0001c0001t0001g0146 a0001c0001t0001g0155 a0001c0001t0002g0009 others(7): Show |
10 | HG02155.hp2 HG02647.hp2 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+6194_99+6198dup others(5): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782279 | ||||||
| chr8:97782279 | C | CTTTTTT | 7 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0003g0032 others(4): Show |
7 | HG00673.hp1 HG02027.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+6193_99+6198dup others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782279 | ||||||
| chr8:97782279 | CT | C | 41 | a0001c0001t0004g0012 a0001c0001t0004g0169 a0001c0001t0004g0173 others(38): Show |
41 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.99+6198delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782279 | ||||||
| chr8:97782279 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0006g0004 a0001c0001t0006g0005 a0001c0001t0006g0007 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+6188_99+6198del others(11): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782279 | ||||||
| chr8:97782315 | A | G | 306 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(303): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.99+6207A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782315 | |||||||
| chr8:97782340 | GTGGCTCA others(18): Show |
G | 65 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(62): Show |
65 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.99+6241_99+6265del others(25): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782340 | ||||||
| chr8:97782348 | AT | A | 28 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(25): Show |
28 | HG00642.hp2 HG00738.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.99+6241delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782348 | |||||||
| chr8:97782369 | C | T | 1 | a0002c0003t0005g0351 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.99+6261C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782369 | |||||||
| chr8:97782542 | G | A | 1 | a0001c0001t0004g0123 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.99+6434G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782542 | |||||||
| chr8:97782653 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.99+6545G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782653 | |||||||
| chr8:97782657 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.99+6549C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782657 | |||||||
| chr8:97782687 | C | T | 5 | a0001c0001t0001g0319 a0001c0001t0007g0031 a0001c0001t0012g0129 others(2): Show |
5 | HG00673.hp2 NA18941.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+6579C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782687 | |||||||
| chr8:97782697 | A | G | 3 | a0001c0001t0006g0004 a0001c0001t0006g0005 a0001c0001t0006g0007 |
3 | HG01891.hp2 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.99+6589A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782697 | |||||||
| chr8:97782725 | C | T | 1 | a0001c0001t0001g0298 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.99+6617C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782725 | |||||||
| chr8:97782877 | A | G | 1 | a0001c0001t0002g0283 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.99+6769A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782877 | |||||||
| chr8:97782906 | T | TTTTA | 103 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(100): Show |
103 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.99+6838_99+6841dup others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782906 | ||||||
| chr8:97782906 | T | TTTTATTT others(1): Show |
98 | a0001c0001t0001g0017 a0001c0001t0001g0054 a0001c0001t0001g0055 others(95): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.99+6834_99+6841dup others(8): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782906 | ||||||
| chr8:97782906 | T | TTTTATTT others(5): Show |
28 | a0001c0001t0001g0099 a0001c0001t0002g0336 a0001c0001t0002g0366 others(25): Show |
28 | HG00280.hp2 HG00639.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.99+6830_99+6841dup others(12): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782906 | ||||||
| chr8:97782906 | T | TTTTATTT others(9): Show |
5 | a0001c0001t0005g0143 a0001c0001t0007g0031 a0001c0001t0011g0072 others(2): Show |
5 | HG00323.hp2 NA18941.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+6826_99+6841dup others(16): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782906 | ||||||
| chr8:97782906 | TTTTA | T | 9 | a0001c0001t0002g0003 a0001c0001t0003g0076 a0001c0001t0005g0006 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+6838_99+6841del others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97782906 | ||||||
| chr8:97782950 | T | A | 1 | a0001c0001t0012g0129 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.99+6842T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97782950 | |||||||
| chr8:97783030 | C | T | 5 | a0001c0001t0001g0300 a0001c0001t0002g0261 a0001c0001t0002g0283 others(2): Show |
5 | HG00639.hp1 HG00642.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+6922C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783030 | |||||||
| chr8:97783071 | C | A | 18 | a0001c0001t0002g0081 a0001c0001t0003g0084 a0001c0001t0005g0025 others(15): Show |
18 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+6963C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783071 | |||||||
| chr8:97783072 | C | CT | 191 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(188): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.99+6983dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97783072 | ||||||
| chr8:97783072 | C | CTT | 21 | a0001c0001t0001g0105 a0001c0001t0001g0293 a0001c0001t0001g0300 others(18): Show |
21 | HG00639.hp1 HG00642.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.99+6982_99+6983dup others(2): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97783072 | ||||||
| chr8:97783072 | C | CTTT | 6 | a0001c0001t0002g0009 a0001c0001t0003g0354 a0001c0001t0003g0356 others(3): Show |
6 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+6981_99+6983dup others(3): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97783072 | ||||||
| chr8:97783072 | C | T | 1 | a0001c0001t0004g0169 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.99+6964C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783072 | |||||||
| chr8:97783072 | CTT | C | 71 | a0001c0001t0001g0087 a0001c0001t0001g0136 a0001c0001t0001g0146 others(68): Show |
71 | HG00673.hp1 HG00733.hp2 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.99+6982_99+6983del others(2): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97783072 | ||||||
| chr8:97783072 | CTTT | C | 6 | a0001c0001t0002g0081 a0001c0001t0002g0141 a0001c0001t0005g0144 others(3): Show |
6 | HG01167.hp1 HG01168.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+6981_99+6983del others(3): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97783072 | ||||||
| chr8:97783187 | T | C | 1 | a0001c0001t0010g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+7079T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783187 | |||||||
| chr8:97783373 | C | T | 2 | a0001c0001t0003g0140 a0001c0001t0006g0161 |
2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.99+7265C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783373 | |||||||
| chr8:97783461 | A | G | 1 | a0001c0001t0003g0114 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.99+7353A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783461 | |||||||
| chr8:97783611 | TGA | T | 4 | a0001c0001t0003g0281 a0001c0001t0003g0286 a0001c0001t0003g0331 others(1): Show |
4 | NA18940.hp2 NA18988.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+7507_99+7508del others(2): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97783611 | ||||||
| chr8:97783674 | A | G | 8 | a0001c0001t0002g0003 a0001c0001t0004g0163 a0001c0001t0005g0006 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+7566A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783674 | |||||||
| chr8:97783774 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.99+7666C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783774 | |||||||
| chr8:97783783 | A | G | 17 | a0001c0001t0002g0038 a0001c0001t0002g0042 a0001c0001t0003g0013 others(14): Show |
17 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+7675A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783783 | |||||||
| chr8:97783815 | A | G | 12 | a0001c0001t0004g0173 a0001c0001t0004g0177 a0001c0001t0004g0191 others(9): Show |
12 | HG00099.hp1 HG00323.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+7707A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783815 | |||||||
| chr8:97783879 | G | A | 1 | a0001c0001t0027g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.99+7771G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783879 | |||||||
| chr8:97783885 | A | G | 13 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(10): Show |
13 | HG01081.hp2 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+7777A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783885 | |||||||
| chr8:97783904 | C | T | 1 | a0001c0001t0036g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99+7796C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783904 | |||||||
| chr8:97783946 | CAA | C | 5 | a0001c0001t0001g0319 a0001c0001t0007g0031 a0001c0001t0012g0129 others(2): Show |
5 | HG00673.hp2 NA18941.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+7840_99+7841del others(2): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97783946 | ||||||
| chr8:97783971 | T | C | 4 | a0001c0001t0001g0258 a0001c0001t0002g0338 a0001c0001t0003g0278 others(1): Show |
4 | HG01099.hp2 HG01978.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+7863T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783971 | |||||||
| chr8:97783984 | A | G | 16 | a0001c0001t0001g0136 a0001c0001t0001g0146 a0001c0001t0001g0147 others(13): Show |
16 | HG00673.hp1 HG02027.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+7876A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97783984 | |||||||
| chr8:97784137 | T | C | 2 | a0001c0001t0002g0358 a0001c0001t0002g0359 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.99+8029T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97784137 | |||||||
| chr8:97784164 | C | T | 1 | a0001c0001t0007g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.99+8056C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97784164 | |||||||
| chr8:97784165 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.99+8057G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97784165 | |||||||
| chr8:97784238 | G | A | 5 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+8130G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97784238 | |||||||
| chr8:97784244 | T | C | 85 | a0001c0001t0001g0087 a0001c0001t0001g0136 a0001c0001t0001g0146 others(82): Show |
85 | HG00673.hp1 HG00733.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.99+8136T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97784244 | |||||||
| chr8:97784333 | A | C | 7 | a0001c0001t0002g0003 a0001c0001t0005g0006 a0001c0001t0006g0002 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+8225A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97784333 | |||||||
| chr8:97784343 | A | G | 1 | a0001c0001t0004g0236 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.99+8235A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97784343 | |||||||
| chr8:97784402 | G | C | 13 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(10): Show |
13 | HG01081.hp2 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+8294G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97784402 | |||||||
| chr8:97784452 | TTTTTTGA others(7): Show |
T | 1 | a0001c0001t0036g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99+8346_99+8359del others(14): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97784452 | ||||||
| chr8:97784470 | C | A | 2 | a0001c0001t0006g0127 a0002c0003t0005g0126 |
2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.99+8362C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97784470 | |||||||
| chr8:97784500 | T | C | 314 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(311): Show |
314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.99+8392T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97784500 | |||||||
| chr8:97784510 | A | G | 24 | a0001c0001t0002g0081 a0001c0001t0002g0139 a0001c0001t0003g0084 others(21): Show |
24 | HG01167.hp1 HG01884.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.99+8402A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97784510 | |||||||
| chr8:97784621 | A | G | 5 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+8513A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97784621 | |||||||
| chr8:97784633 | T | G | 128 | a0001c0001t0001g0052 a0001c0001t0001g0133 a0001c0001t0001g0153 others(125): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.99+8525T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97784633 | |||||||
| chr8:97785146 | T | C | 5 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+9038T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97785146 | |||||||
| chr8:97785195 | C | T | 5 | a0001c0001t0001g0319 a0001c0001t0007g0031 a0001c0001t0012g0129 others(2): Show |
5 | HG00673.hp2 NA18941.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+9087C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97785195 | |||||||
| chr8:97785205 | C | G | 1 | a0001c0001t0007g0170 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.99+9097C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97785205 | |||||||
| chr8:97785291 | G | A | 3 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.99+9183G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97785291 | |||||||
| chr8:97785320 | G | A | 1 | a0001c0002t0018g0242 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.99+9212G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97785320 | |||||||
| chr8:97785408 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.99+9300G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97785408 | |||||||
| chr8:97785454 | A | G | 21 | a0001c0001t0001g0136 a0001c0001t0001g0146 a0001c0001t0001g0147 others(18): Show |
21 | HG00673.hp1 HG02027.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+9346A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97785454 | |||||||
| chr8:97785463 | G | A | 5 | a0001c0001t0001g0319 a0001c0001t0007g0031 a0001c0001t0012g0129 others(2): Show |
5 | HG00673.hp2 NA18941.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+9355G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97785463 | |||||||
| chr8:97785499 | GGAA | G | 6 | a0001c0001t0004g0181 a0001c0001t0004g0189 a0001c0001t0004g0203 others(3): Show |
6 | HG01192.hp2 HG01261.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+9396_99+9398del others(3): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97785499 | ||||||
| chr8:97785582 | C | T | 1 | a0001c0001t0001g0344 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.99+9474C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97785582 | |||||||
| chr8:97785620 | A | G | 1 | a0001c0001t0002g0336 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.99+9512A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97785620 | |||||||
| chr8:97785854 | A | C | 13 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0001g0088 others(10): Show |
13 | HG00609.hp1 HG02027.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+9746A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97785854 | |||||||
| chr8:97785889 | C | T | 5 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+9781C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97785889 | |||||||
| chr8:97786160 | T | G | 1 | a0001c0001t0033g0047 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.99+10052T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97786160 | |||||||
| chr8:97786241 | A | C | 7 | a0001c0001t0002g0003 a0001c0001t0005g0006 a0001c0001t0006g0002 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+10133A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97786241 | |||||||
| chr8:97786252 | T | G | 1 | a0001c0001t0002g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.99+10144T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97786252 | |||||||
| chr8:97786334 | A | G | 16 | a0001c0001t0002g0081 a0001c0001t0003g0084 a0001c0001t0005g0080 others(13): Show |
16 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+10226A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97786334 | |||||||
| chr8:97786408 | T | TAAAA | 282 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(279): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.99+10307_99+10310d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97786408 | ||||||
| chr8:97786408 | T | TAAAAA | 32 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0003 others(29): Show |
32 | HG00558.hp1 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.99+10306_99+10310d others(7): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97786408 | ||||||
| chr8:97786419 | C | G | 1 | a0001c0001t0030g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.99+10311C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97786419 | |||||||
| chr8:97786533 | C | G | 1 | a0001c0001t0007g0170 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.99+10425C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97786533 | |||||||
| chr8:97786580 | T | A | 1 | a0001c0001t0002g0288 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.99+10472T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97786580 | |||||||
| chr8:97786605 | C | G | 1 | a0001c0001t0007g0170 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.99+10497C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97786605 | |||||||
| chr8:97786605 | C | T | 3 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.99+10497C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97786605 | |||||||
| chr8:97786635 | G | A | 52 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(49): Show |
52 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.99+10527G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97786635 | |||||||
| chr8:97786673 | C | T | 2 | a0001c0001t0002g0366 a0001c0001t0002g0369 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.99+10565C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97786673 | |||||||
| chr8:97786700 | A | AG | 21 | a0001c0001t0001g0087 a0001c0001t0007g0195 a0001c0001t0007g0228 others(18): Show |
21 | HG00741.hp1 HG00741.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+10593dupG | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97786700 | ||||||
| chr8:97786701 | G | GA | 36 | a0001c0001t0001g0056 a0001c0001t0001g0088 a0001c0001t0001g0102 others(33): Show |
36 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.99+10609dupA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97786701 | ||||||
| chr8:97786701 | GA | G | 8 | a0001c0001t0001g0111 a0001c0001t0003g0140 a0001c0001t0003g0274 others(5): Show |
8 | HG01243.hp2 HG01361.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+10609delA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97786701 | ||||||
| chr8:97786715 | A | C | 1 | a0001c0001t0027g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.99+10607A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97786715 | |||||||
| chr8:97786717 | A | AAC | 19 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0120 others(16): Show |
19 | HG00642.hp2 HG00738.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+10609_99+10610i others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97786717 | |||||||
| chr8:97787035 | T | A | 1 | a0001c0001t0004g0183 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.99+10927T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787035 | |||||||
| chr8:97787108 | C | G | 1 | a0001c0002t0009g0251 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+11000C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787108 | |||||||
| chr8:97787177 | T | A | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 others(1): Show |
4 | HG02647.hp2 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+11069T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787177 | |||||||
| chr8:97787186 | G | A | 1 | a0001c0001t0002g0345 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.99+11078G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787186 | |||||||
| chr8:97787279 | GTTTC | G | 65 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(62): Show |
65 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.99+11179_99+11182d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97787279 | ||||||
| chr8:97787287 | C | CTT | 56 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0062 others(53): Show |
56 | HG00099.hp1 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.99+11194_99+11195d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97787287 | ||||||
| chr8:97787309 | T | C | 368 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(365): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.99+11201T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787309 | |||||||
| chr8:97787379 | A | G | 180 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.99+11271A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787379 | |||||||
| chr8:97787381 | G | A | 1 | a0001c0001t0011g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.99+11273G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787381 | |||||||
| chr8:97787410 | C | T | 18 | a0001c0001t0001g0087 a0001c0001t0002g0338 a0001c0001t0003g0069 others(15): Show |
18 | HG00733.hp2 HG01081.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+11302C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787410 | |||||||
| chr8:97787411 | G | A | 10 | a0001c0001t0005g0025 a0001c0001t0008g0019 a0001c0001t0008g0020 others(7): Show |
10 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+11303G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787411 | |||||||
| chr8:97787430 | C | T | 2 | a0001c0001t0003g0114 a0001c0001t0031g0030 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.99+11322C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787430 | |||||||
| chr8:97787475 | A | G | 2 | a0001c0001t0003g0114 a0001c0001t0031g0030 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.99+11367A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787475 | |||||||
| chr8:97787639 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.99+11531T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787639 | |||||||
| chr8:97787654 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.99+11546G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787654 | |||||||
| chr8:97787690 | G | T | 18 | a0001c0001t0001g0087 a0001c0001t0002g0338 a0001c0001t0003g0069 others(15): Show |
18 | HG00733.hp2 HG01081.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+11582G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787690 | |||||||
| chr8:97787727 | A | G | 369 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(366): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.99+11619A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787727 | |||||||
| chr8:97787760 | C | T | 1 | a0001c0001t0001g0353 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.99+11652C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787760 | |||||||
| chr8:97787791 | T | C | 1 | a0001c0001t0006g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.99+11683T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787791 | |||||||
| chr8:97787812 | A | G | 21 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0003g0071 others(18): Show |
21 | HG00735.hp2 HG00738.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.99+11704A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97787812 | |||||||
| chr8:97788097 | C | T | 1 | a0001c0001t0002g0261 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.99+11989C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97788097 | |||||||
| chr8:97788106 | A | C | 62 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(59): Show |
62 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.99+11998A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97788106 | |||||||
| chr8:97788124 | G | C | 2 | a0001c0001t0003g0267 a0001c0001t0003g0274 |
2 | NA18939.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.99+12016G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97788124 | |||||||
| chr8:97788160 | G | C | 366 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(363): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.99+12052G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97788160 | |||||||
| chr8:97788192 | C | T | 68 | a0001c0001t0001g0018 a0001c0001t0001g0133 a0001c0001t0001g0136 others(65): Show |
68 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.99+12084C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97788192 | |||||||
| chr8:97788263 | C | T | 369 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(366): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.99+12155C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97788263 | |||||||
| chr8:97788389 | G | A | 1 | a0001c0001t0036g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99+12281G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97788389 | |||||||
| chr8:97788619 | A | G | 1 | a0001c0001t0002g0329 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.99+12511A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97788619 | |||||||
| chr8:97788700 | A | AT | 170 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(167): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.99+12604dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97788700 | ||||||
| chr8:97788700 | AT | A | 8 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(5): Show |
8 | HG01081.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+12604delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97788700 | ||||||
| chr8:97788785 | C | G | 6 | a0001c0001t0002g0338 a0001c0001t0003g0278 a0001c0001t0003g0285 others(3): Show |
6 | HG00733.hp2 HG01099.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+12677C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97788785 | |||||||
| chr8:97788793 | C | T | 2 | a0001c0001t0027g0302 a0001c0002t0009g0251 |
2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.99+12685C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97788793 | |||||||
| chr8:97788844 | G | A | 9 | a0001c0001t0002g0003 a0001c0001t0005g0006 a0001c0001t0006g0002 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+12736G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97788844 | |||||||
| chr8:97789038 | C | CTTTA | 7 | a0001c0001t0003g0372 a0001c0001t0003g0373 a0001c0001t0004g0175 others(4): Show |
7 | HG00673.hp2 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+12978_99+12981d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97789038 | ||||||
| chr8:97789038 | CTTTA | C | 58 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0066 others(55): Show |
58 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(55): Show |
intron_variant | MODIFIER | c.99+12978_99+12981d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97789038 | ||||||
| chr8:97789038 | CTTTATTT others(1): Show |
C | 134 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(131): Show |
134 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.99+12974_99+12981d others(10): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97789038 | ||||||
| chr8:97789038 | CTTTATTT others(5): Show |
C | 15 | a0001c0001t0002g0139 a0001c0001t0003g0327 a0001c0001t0004g0173 others(12): Show |
15 | HG00323.hp2 HG01106.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+12970_99+12981d others(14): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97789038 | ||||||
| chr8:97789038 | CTTTATTT others(9): Show |
C | 18 | a0001c0001t0001g0272 a0001c0001t0001g0317 a0001c0001t0002g0271 others(15): Show |
18 | HG00741.hp1 HG02109.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+12966_99+12981d others(18): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97789038 | ||||||
| chr8:97789038 | CTTTATTT others(13): Show |
C | 118 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(115): Show |
118 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.99+12962_99+12981d others(22): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97789038 | ||||||
| chr8:97789040 | TTATTTAT others(11): Show |
T | 7 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(4): Show |
7 | HG01256.hp1 HG01258.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+12934_99+12951d others(20): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97789040 | ||||||
| chr8:97789072 | T | A | 2 | a0001c0001t0027g0302 a0001c0002t0009g0251 |
2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.99+12964T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97789072 | |||||||
| chr8:97789196 | C | T | 61 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(58): Show |
61 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.99+13088C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97789196 | |||||||
| chr8:97789230 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.99+13122C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97789230 | |||||||
| chr8:97789235 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.99+13127G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97789235 | |||||||
| chr8:97789340 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.99+13232C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97789340 | |||||||
| chr8:97789375 | G | GT | 169 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(166): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.99+13274dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97789375 | ||||||
| chr8:97789525 | A | AT | 6 | a0001c0001t0001g0100 a0001c0001t0004g0229 a0001c0001t0005g0321 others(3): Show |
6 | HG00735.hp1 HG01952.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+13434dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97789525 | ||||||
| chr8:97789525 | AT | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0001g0111 others(9): Show |
12 | HG01169.hp2 HG01256.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+13434delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97789525 | ||||||
| chr8:97789530 | T | TG | 18 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(15): Show |
18 | HG01081.hp2 HG02109.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+13422_99+13423i others(3): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97789530 | |||||||
| chr8:97789540 | T | G | 2 | a0001c0002t0009g0375 a0001c0002t0009g0377 |
2 | HG03710.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.99+13432T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97789540 | |||||||
| chr8:97789601 | C | G | 57 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0066 others(54): Show |
57 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.99+13493C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97789601 | |||||||
| chr8:97789632 | A | G | 18 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(15): Show |
18 | HG01081.hp2 HG02109.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+13524A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97789632 | |||||||
| chr8:97789772 | C | T | 3 | a0001c0001t0006g0039 a0001c0001t0022g0048 a0003c0006t0005g0034 |
3 | HG02572.hp2 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.99+13664C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97789772 | |||||||
| chr8:97789838 | T | G | 1 | a0001c0001t0002g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99+13730T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97789838 | |||||||
| chr8:97789915 | C | T | 2 | a0001c0001t0002g0079 a0001c0001t0002g0116 |
2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+13807C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97789915 | |||||||
| chr8:97789998 | A | G | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 others(1): Show |
4 | HG02647.hp2 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+13890A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97789998 | |||||||
| chr8:97790150 | T | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0066 others(56): Show |
59 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.99+14042T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97790150 | |||||||
| chr8:97790166 | G | A | 173 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(170): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.99+14058G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97790166 | |||||||
| chr8:97790185 | AT | A | 369 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(366): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.99+14087delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97790185 | ||||||
| chr8:97790188 | T | C | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 others(1): Show |
4 | HG02647.hp2 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+14080T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97790188 | |||||||
| chr8:97790197 | A | G | 18 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(15): Show |
18 | HG01081.hp2 HG02109.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+14089A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97790197 | |||||||
| chr8:97790238 | G | A | 4 | a0001c0001t0005g0080 a0001c0001t0005g0124 a0001c0001t0006g0082 others(1): Show |
4 | HG01167.hp1 HG02486.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+14130G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97790238 | |||||||
| chr8:97790315 | AT | A | 9 | a0001c0001t0001g0014 a0001c0001t0003g0084 a0001c0001t0003g0281 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+14223delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97790315 | ||||||
| chr8:97790316 | T | C | 1 | a0001c0001t0007g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.99+14208T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97790316 | |||||||
| chr8:97790351 | C | T | 8 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(5): Show |
8 | HG01081.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+14243C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97790351 | |||||||
| chr8:97790379 | C | T | 1 | a0001c0001t0005g0361 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.99+14271C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97790379 | |||||||
| chr8:97790500 | T | C | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 others(1): Show |
4 | HG02647.hp2 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+14392T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97790500 | |||||||
| chr8:97790644 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.99+14536C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97790644 | |||||||
| chr8:97790770 | G | A | 20 | a0001c0001t0001g0087 a0001c0001t0002g0338 a0001c0001t0003g0069 others(17): Show |
20 | HG00733.hp2 HG01081.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.100-14583G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97790770 | |||||||
| chr8:97790973 | C | T | 5 | a0001c0001t0002g0367 a0001c0001t0005g0143 a0001c0001t0005g0144 others(2): Show |
5 | HG02258.hp1 HG02486.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-14380C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97790973 | |||||||
| chr8:97790989 | C | T | 4 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-14364C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97790989 | |||||||
| chr8:97791392 | C | G | 1 | a0001c0001t0003g0086 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.100-13961C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97791392 | |||||||
| chr8:97791393 | C | A | 1 | a0001c0001t0001g0333 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.100-13960C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97791393 | |||||||
| chr8:97791450 | G | T | 1 | a0001c0001t0003g0064 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.100-13903G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97791450 | |||||||
| chr8:97791501 | C | T | 168 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(165): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.100-13852C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97791501 | |||||||
| chr8:97791564 | C | G | 6 | a0001c0001t0003g0281 a0001c0001t0003g0286 a0001c0001t0003g0331 others(3): Show |
6 | HG00438.hp1 NA18940.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-13789C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97791564 | |||||||
| chr8:97791593 | C | T | 1 | a0001c0001t0002g0288 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.100-13760C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97791593 | |||||||
| chr8:97791604 | C | T | 1 | a0001c0002t0009g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100-13749C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97791604 | |||||||
| chr8:97791687 | T | G | 6 | a0001c0001t0003g0084 a0001c0001t0003g0140 a0001c0001t0006g0119 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-13666T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97791687 | |||||||
| chr8:97791741 | C | T | 1 | a0001c0002t0015g0249 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.100-13612C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97791741 | |||||||
| chr8:97791787 | G | A | 9 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-13566G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97791787 | |||||||
| chr8:97791947 | C | T | 3 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.100-13406C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97791947 | |||||||
| chr8:97792143 | G | C | 172 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(169): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.100-13210G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97792143 | |||||||
| chr8:97792165 | G | A | 6 | a0001c0001t0003g0084 a0001c0001t0003g0140 a0001c0001t0006g0119 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-13188G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97792165 | |||||||
| chr8:97792381 | G | A | 369 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(366): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.100-12972G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97792381 | |||||||
| chr8:97792428 | G | A | 10 | a0001c0001t0005g0025 a0001c0001t0008g0019 a0001c0001t0008g0020 others(7): Show |
10 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-12925G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97792428 | |||||||
| chr8:97792463 | C | T | 136 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(133): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.100-12890C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97792463 | |||||||
| chr8:97792496 | C | G | 1 | a0001c0002t0015g0245 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.100-12857C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97792496 | |||||||
| chr8:97792559 | A | G | 63 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(60): Show |
63 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.100-12794A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97792559 | |||||||
| chr8:97792560 | G | T | 1 | a0001c0001t0001g0024 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.100-12793G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97792560 | |||||||
| chr8:97792564 | AT | A | 7 | a0001c0001t0003g0084 a0001c0001t0003g0140 a0001c0001t0006g0119 others(4): Show |
7 | HG01167.hp2 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-12779delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97792564 | ||||||
| chr8:97792592 | T | C | 198 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(195): Show |
198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.100-12761T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97792592 | |||||||
| chr8:97792611 | T | A | 369 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(366): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.100-12742T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97792611 | |||||||
| chr8:97792929 | A | G | 2 | a0001c0005t0001g0016 a0001c0005t0001g0023 |
2 | HG00558.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.100-12424A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97792929 | |||||||
| chr8:97793043 | G | GA | 87 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0066 others(84): Show |
87 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-12301dupA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97793043 | ||||||
| chr8:97793043 | GA | G | 198 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(195): Show |
198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.100-12301delA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97793043 | ||||||
| chr8:97793213 | A | G | 6 | a0001c0001t0003g0084 a0001c0001t0003g0140 a0001c0001t0006g0119 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-12140A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97793213 | |||||||
| chr8:97793287 | A | G | 1 | a0001c0001t0031g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-12066A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97793287 | |||||||
| chr8:97793412 | A | G | 1 | a0001c0001t0002g0303 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.100-11941A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97793412 | |||||||
| chr8:97793501 | T | C | 2 | a0001c0001t0003g0308 a0001c0001t0007g0370 |
2 | HG01243.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.100-11852T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97793501 | |||||||
| chr8:97793541 | C | T | 1 | a0001c0001t0036g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100-11812C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97793541 | |||||||
| chr8:97793579 | G | A | 1 | a0001c0001t0005g0145 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.100-11774G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97793579 | |||||||
| chr8:97793682 | A | G | 3 | a0001c0001t0011g0057 a0001c0002t0019g0164 a0001c0002t0019g0246 |
3 | HG00280.hp1 HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.100-11671A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97793682 | |||||||
| chr8:97793701 | T | C | 4 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-11652T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97793701 | |||||||
| chr8:97793713 | G | A | 1 | a0001c0001t0016g0352 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.100-11640G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97793713 | |||||||
| chr8:97793767 | A | G | 204 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(201): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.100-11586A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97793767 | |||||||
| chr8:97793866 | G | A | 1 | a0001c0001t0006g0007 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.100-11487G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97793866 | |||||||
| chr8:97793948 | C | A | 79 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0066 others(76): Show |
79 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.100-11405C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97793948 | |||||||
| chr8:97794036 | A | G | 1 | a0001c0001t0030g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100-11317A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794036 | |||||||
| chr8:97794257 | G | A | 1 | a0001c0001t0004g0232 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.100-11096G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794257 | |||||||
| chr8:97794323 | G | C | 172 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(169): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.100-11030G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794323 | |||||||
| chr8:97794511 | G | A | 1 | a0001c0001t0004g0199 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.100-10842G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794511 | |||||||
| chr8:97794557 | T | A | 6 | a0001c0001t0003g0084 a0001c0001t0003g0140 a0001c0001t0006g0119 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-10796T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794557 | |||||||
| chr8:97794601 | T | TA | 57 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0066 others(54): Show |
57 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.100-10751dupA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97794601 | ||||||
| chr8:97794602 | A | G | 1 | a0001c0002t0021g0244 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.100-10751A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794602 | |||||||
| chr8:97794707 | T | A | 3 | a0001c0001t0002g0332 a0001c0001t0006g0127 a0002c0003t0005g0126 |
3 | HG02055.hp2 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.100-10646T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794707 | |||||||
| chr8:97794758 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.100-10595C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794758 | |||||||
| chr8:97794759 | G | A | 3 | a0002c0003t0013g0190 a0002c0003t0013g0215 a0002c0003t0013g0216 |
3 | HG01515.hp2 HG01517.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.100-10594G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794759 | |||||||
| chr8:97794805 | C | T | 1 | a0001c0001t0027g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.100-10548C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794805 | |||||||
| chr8:97794891 | T | G | 155 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(152): Show |
155 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.100-10462T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794891 | |||||||
| chr8:97794927 | G | T | 2 | a0001c0001t0003g0084 a0001c0001t0006g0119 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.100-10426G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794927 | |||||||
| chr8:97794965 | G | T | 20 | a0001c0001t0002g0038 a0001c0001t0002g0042 a0001c0001t0003g0013 others(17): Show |
20 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.100-10388G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794965 | |||||||
| chr8:97794976 | T | C | 2 | a0001c0001t0003g0114 a0001c0001t0031g0030 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100-10377T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794976 | |||||||
| chr8:97794978 | C | G | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100-10375C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794978 | |||||||
| chr8:97794989 | G | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100-10364G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97794989 | |||||||
| chr8:97795000 | C | G | 64 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(61): Show |
64 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.100-10353C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795000 | |||||||
| chr8:97795012 | C | G | 11 | a0001c0001t0004g0173 a0001c0001t0004g0177 a0001c0001t0004g0191 others(8): Show |
11 | HG00099.hp1 HG00323.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-10341C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795012 | |||||||
| chr8:97795196 | C | T | 3 | a0001c0001t0003g0354 a0001c0001t0003g0356 a0001c0001t0016g0352 |
3 | HG00438.hp2 NA18977.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.100-10157C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795196 | |||||||
| chr8:97795320 | T | G | 205 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(202): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.100-10033T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795320 | |||||||
| chr8:97795484 | G | T | 6 | a0001c0001t0003g0084 a0001c0001t0003g0140 a0001c0001t0006g0119 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-9869G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795484 | |||||||
| chr8:97795502 | C | T | 1 | a0001c0001t0003g0311 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.100-9851C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795502 | |||||||
| chr8:97795636 | T | A | 2 | a0001c0001t0027g0302 a0001c0002t0009g0251 |
2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.100-9717T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795636 | |||||||
| chr8:97795643 | A | G | 2 | a0001c0001t0003g0114 a0001c0001t0031g0030 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100-9710A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795643 | |||||||
| chr8:97795736 | C | T | 199 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.100-9617C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795736 | |||||||
| chr8:97795800 | G | A | 1 | a0001c0001t0007g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100-9553G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795800 | |||||||
| chr8:97795802 | A | C | 1 | a0001c0001t0005g0157 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.100-9551A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795802 | |||||||
| chr8:97795807 | A | G | 199 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.100-9546A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795807 | |||||||
| chr8:97795820 | A | G | 205 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(202): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.100-9533A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795820 | |||||||
| chr8:97795837 | T | TA | 201 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0024 others(198): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.100-9494dupA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97795837 | ||||||
| chr8:97795837 | T | TAA | 11 | a0001c0001t0001g0014 a0001c0001t0002g0139 a0001c0001t0002g0277 others(8): Show |
11 | HG00438.hp2 HG01884.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-9495_100-9494d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97795837 | ||||||
| chr8:97795837 | TA | T | 14 | a0001c0001t0002g0149 a0001c0001t0003g0069 a0001c0001t0004g0175 others(11): Show |
14 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-9494delA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97795837 | ||||||
| chr8:97795837 | TAAAAAAA others(6): Show |
T | 4 | a0001c0001t0001g0273 a0001c0001t0001g0291 a0001c0001t0001g0298 others(1): Show |
4 | NA18949.hp1 NA18954.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-9506_100-9494d others(15): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97795837 | ||||||
| chr8:97795889 | C | A | 2 | a0001c0001t0003g0262 a0001c0001t0007g0171 |
2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.100-9464C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795889 | |||||||
| chr8:97795929 | A | C | 199 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.100-9424A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795929 | |||||||
| chr8:97795957 | G | A | 6 | a0001c0001t0003g0084 a0001c0001t0003g0140 a0001c0001t0006g0119 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-9396G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795957 | |||||||
| chr8:97795967 | C | G | 10 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0002g0117 others(7): Show |
10 | HG00280.hp1 HG00741.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-9386C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97795967 | |||||||
| chr8:97796036 | C | T | 1 | a0001c0001t0004g0191 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.100-9317C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796036 | |||||||
| chr8:97796058 | GC | G | 291 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.100-9288delC | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97796058 | ||||||
| chr8:97796067 | G | C | 4 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-9286G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796067 | |||||||
| chr8:97796100 | C | T | 1 | a0001c0002t0017g0240 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.100-9253C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796100 | |||||||
| chr8:97796141 | G | A | 20 | a0001c0001t0002g0038 a0001c0001t0002g0042 a0001c0001t0003g0013 others(17): Show |
20 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.100-9212G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796141 | |||||||
| chr8:97796171 | C | G | 4 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-9182C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796171 | |||||||
| chr8:97796203 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.100-9150A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796203 | |||||||
| chr8:97796304 | A | G | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.100-9049A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796304 | |||||||
| chr8:97796397 | C | T | 68 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(65): Show |
68 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.100-8956C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796397 | |||||||
| chr8:97796425 | C | G | 2 | a0001c0001t0010g0252 a0001c0001t0010g0253 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.100-8928C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796425 | |||||||
| chr8:97796441 | G | A | 63 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(60): Show |
63 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.100-8912G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796441 | |||||||
| chr8:97796563 | A | G | 6 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0104 others(3): Show |
6 | HG00423.hp1 HG02015.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-8790A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796563 | |||||||
| chr8:97796644 | A | G | 131 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(128): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.100-8709A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796644 | |||||||
| chr8:97796897 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.100-8456G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796897 | |||||||
| chr8:97796941 | A | G | 199 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.100-8412A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97796941 | |||||||
| chr8:97797034 | G | A | 1 | a0001c0001t0029g0374 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.100-8319G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797034 | |||||||
| chr8:97797042 | C | T | 199 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.100-8311C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797042 | |||||||
| chr8:97797099 | A | G | 1 | a0001c0001t0011g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.100-8254A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797099 | |||||||
| chr8:97797111 | A | G | 1 | a0001c0001t0002g0277 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.100-8242A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797111 | |||||||
| chr8:97797131 | A | T | 1 | a0001c0001t0002g0277 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.100-8222A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797131 | |||||||
| chr8:97797138 | C | CT | 263 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(260): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.100-8202dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97797138 | ||||||
| chr8:97797138 | C | CTT | 27 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(24): Show |
27 | HG00733.hp1 HG00738.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.100-8203_100-8202d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97797138 | ||||||
| chr8:97797159 | A | G | 199 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.100-8194A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797159 | |||||||
| chr8:97797361 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0128 |
2 | HG01433.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.100-7992G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797361 | |||||||
| chr8:97797376 | T | G | 369 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(366): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.100-7977T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797376 | |||||||
| chr8:97797381 | C | T | 6 | a0001c0001t0003g0084 a0001c0001t0003g0140 a0001c0001t0006g0119 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-7972C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797381 | |||||||
| chr8:97797385 | A | G | 205 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(202): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.100-7968A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797385 | |||||||
| chr8:97797422 | C | T | 1 | a0001c0002t0018g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-7931C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797422 | |||||||
| chr8:97797424 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0353 |
2 | NA19077.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.100-7929C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797424 | |||||||
| chr8:97797428 | C | T | 1 | a0001c0001t0005g0044 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100-7925C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797428 | |||||||
| chr8:97797529 | G | C | 6 | a0001c0001t0003g0084 a0001c0001t0003g0140 a0001c0001t0006g0119 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-7824G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797529 | |||||||
| chr8:97797597 | A | G | 199 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.100-7756A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797597 | |||||||
| chr8:97797624 | A | T | 5 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-7729A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797624 | |||||||
| chr8:97797691 | A | AT | 216 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(213): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.100-7654dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97797691 | ||||||
| chr8:97797966 | A | G | 206 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(203): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.100-7387A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97797966 | |||||||
| chr8:97798024 | C | CATTAGCT others(2): Show |
200 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(197): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.100-7327_100-7326i others(11): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97798024 | ||||||
| chr8:97798027 | A | T | 200 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0061 others(197): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.100-7326A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97798027 | |||||||
| chr8:97798097 | G | A | 2 | a0001c0001t0003g0114 a0001c0001t0031g0030 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100-7256G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97798097 | |||||||
| chr8:97798189 | A | C | 10 | a0001c0001t0005g0025 a0001c0001t0008g0019 a0001c0001t0008g0020 others(7): Show |
10 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-7164A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97798189 | |||||||
| chr8:97798331 | G | A | 2 | a0001c0002t0020g0376 a0001c0002t0020g0379 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.100-7022G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97798331 | |||||||
| chr8:97798411 | A | G | 6 | a0001c0001t0003g0084 a0001c0001t0003g0140 a0001c0001t0006g0119 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-6942A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97798411 | |||||||
| chr8:97798564 | G | A | 84 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0066 others(81): Show |
84 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.100-6789G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97798564 | |||||||
| chr8:97798578 | A | G | 1 | a0002c0003t0013g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100-6775A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97798578 | |||||||
| chr8:97798683 | CA | C | 3 | a0001c0001t0003g0262 a0001c0001t0006g0118 a0001c0001t0007g0171 |
3 | HG02280.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.100-6669delA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97798683 | |||||||
| chr8:97798762 | C | CT | 5 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-6590dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97798762 | ||||||
| chr8:97798833 | A | C | 3 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.100-6520A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97798833 | |||||||
| chr8:97798906 | C | G | 161 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0077 others(158): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.100-6447C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97798906 | |||||||
| chr8:97799097 | G | A | 1 | a0001c0001t0025g0292 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.100-6256G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799097 | |||||||
| chr8:97799355 | C | T | 88 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0056 others(85): Show |
88 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.100-5998C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799355 | |||||||
| chr8:97799396 | C | T | 1 | a0001c0001t0011g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.100-5957C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799396 | |||||||
| chr8:97799422 | G | C | 1 | a0001c0001t0003g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100-5931G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799422 | |||||||
| chr8:97799447 | T | G | 370 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(367): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.100-5906T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799447 | |||||||
| chr8:97799469 | G | A | 80 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0056 others(77): Show |
80 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.100-5884G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799469 | |||||||
| chr8:97799584 | C | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.100-5769C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799584 | |||||||
| chr8:97799699 | T | G | 1 | a0001c0001t0002g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.100-5654T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799699 | |||||||
| chr8:97799733 | T | C | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 others(1): Show |
4 | HG01891.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-5620T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799733 | |||||||
| chr8:97799757 | G | A | 119 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(116): Show |
119 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.100-5596G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799757 | |||||||
| chr8:97799780 | C | T | 1 | a0001c0001t0002g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.100-5573C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799780 | |||||||
| chr8:97799834 | C | T | 1 | a0001c0001t0023g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.100-5519C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799834 | |||||||
| chr8:97799961 | T | C | 201 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(198): Show |
201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.100-5392T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799961 | |||||||
| chr8:97799961 | T | G | 8 | a0001c0001t0003g0084 a0001c0001t0005g0025 a0001c0001t0005g0080 others(5): Show |
8 | HG01167.hp1 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-5392T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97799961 | |||||||
| chr8:97800020 | C | G | 219 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(216): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.100-5333C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800020 | |||||||
| chr8:97800052 | C | A | 1 | a0001c0001t0004g0123 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.100-5301C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800052 | |||||||
| chr8:97800074 | A | G | 1 | a0001c0001t0004g0199 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.100-5279A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800074 | |||||||
| chr8:97800202 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-5151G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800202 | |||||||
| chr8:97800255 | G | A | 32 | a0001c0001t0001g0256 a0001c0001t0001g0275 a0001c0001t0001g0294 others(29): Show |
32 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(29): Show |
intron_variant | MODIFIER | c.100-5098G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800255 | |||||||
| chr8:97800307 | A | G | 9 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-5046A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800307 | |||||||
| chr8:97800335 | A | G | 120 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(117): Show |
120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.100-5018A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800335 | |||||||
| chr8:97800399 | C | G | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.100-4954C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800399 | |||||||
| chr8:97800484 | C | CT | 29 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0001g0133 others(26): Show |
29 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.100-4842dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | C | CTT | 18 | a0001c0001t0001g0263 a0001c0001t0001g0306 a0001c0001t0001g0307 others(15): Show |
18 | HG01192.hp2 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.100-4843_100-4842d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | C | CTTT | 6 | a0001c0001t0001g0111 a0001c0001t0002g0360 a0001c0001t0006g0002 others(3): Show |
6 | HG01081.hp2 HG01934.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-4844_100-4842d others(5): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100-4851_100-4842d others(12): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0036g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100-4854_100-4842d others(15): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0008g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.100-4855_100-4842d others(16): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0008g0020 a0001c0001t0008g0021 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-4857_100-4842d others(18): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0008g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.100-4862_100-4842d others(23): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0008g0026 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.100-4864_100-4842d others(25): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0006g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.100-4865_100-4842d others(26): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | C | CTTTTTTT others(22): Show |
2 | a0001c0001t0008g0022 a0001c0001t0008g0027 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.100-4842_100-4841i others(31): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | CT | C | 71 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(68): Show |
71 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.100-4842delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | CTTTTTT | C | 126 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0056 others(123): Show |
126 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.100-4847_100-4842d others(8): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | CTTTTTTT | C | 8 | a0001c0001t0003g0262 a0001c0001t0003g0267 a0001c0001t0003g0314 others(5): Show |
8 | HG00558.hp2 HG01169.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-4848_100-4842d others(9): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800484 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.100-4857_100-4842d others(18): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97800484 | ||||||
| chr8:97800527 | G | A | 131 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(128): Show |
131 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.100-4826G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800527 | |||||||
| chr8:97800530 | T | C | 180 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.100-4823T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800530 | |||||||
| chr8:97800573 | G | C | 180 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.100-4780G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800573 | |||||||
| chr8:97800582 | C | T | 1 | a0001c0001t0002g0283 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.100-4771C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800582 | |||||||
| chr8:97800583 | G | A | 1 | a0001c0001t0036g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100-4770G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800583 | |||||||
| chr8:97800591 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100-4762G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800591 | |||||||
| chr8:97800643 | T | C | 1 | a0001c0001t0003g0285 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.100-4710T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800643 | |||||||
| chr8:97800652 | A | G | 2 | a0001c0002t0020g0376 a0001c0002t0020g0379 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.100-4701A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800652 | |||||||
| chr8:97800657 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100-4696C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800657 | |||||||
| chr8:97800675 | T | A | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-4678T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800675 | |||||||
| chr8:97800693 | T | G | 64 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0056 others(61): Show |
64 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.100-4660T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800693 | |||||||
| chr8:97800742 | C | T | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-4611C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800742 | |||||||
| chr8:97800743 | G | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.100-4610G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800743 | |||||||
| chr8:97800849 | C | T | 1 | a0001c0002t0015g0167 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100-4504C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800849 | |||||||
| chr8:97800871 | G | A | 64 | a0001c0001t0001g0256 a0001c0001t0001g0264 a0001c0001t0001g0270 others(61): Show |
64 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.100-4482G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800871 | |||||||
| chr8:97800969 | G | A | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-4384G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97800969 | |||||||
| chr8:97801011 | C | T | 21 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(18): Show |
21 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.100-4342C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801011 | |||||||
| chr8:97801131 | G | A | 370 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(367): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.100-4222G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801131 | |||||||
| chr8:97801179 | C | CT | 37 | a0001c0001t0001g0018 a0001c0001t0001g0087 a0001c0001t0001g0136 others(34): Show |
37 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.100-4158dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97801179 | ||||||
| chr8:97801179 | CT | C | 217 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(214): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.100-4158delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97801179 | ||||||
| chr8:97801218 | G | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.100-4135G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801218 | |||||||
| chr8:97801235 | A | G | 2 | a0001c0001t0003g0114 a0001c0001t0031g0030 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100-4118A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801235 | |||||||
| chr8:97801243 | A | G | 1 | a0001c0001t0011g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.100-4110A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801243 | |||||||
| chr8:97801272 | A | G | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-4081A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801272 | |||||||
| chr8:97801274 | T | C | 180 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.100-4079T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801274 | |||||||
| chr8:97801284 | C | T | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-4069C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801284 | |||||||
| chr8:97801285 | G | A | 37 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(34): Show |
37 | HG00733.hp1 HG00738.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.100-4068G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801285 | |||||||
| chr8:97801409 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.100-3944T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801409 | |||||||
| chr8:97801447 | G | T | 2 | a0001c0001t0027g0302 a0001c0002t0009g0251 |
2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.100-3906G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801447 | |||||||
| chr8:97801472 | A | G | 5 | a0001c0001t0002g0038 a0001c0001t0002g0042 a0001c0001t0002g0079 others(2): Show |
5 | HG02257.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-3881A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801472 | |||||||
| chr8:97801519 | C | G | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.100-3834C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801519 | |||||||
| chr8:97801627 | A | G | 180 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.100-3726A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801627 | |||||||
| chr8:97801644 | C | T | 1 | a0001c0001t0003g0285 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.100-3709C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801644 | |||||||
| chr8:97801658 | A | G | 14 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0003g0073 others(11): Show |
14 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-3695A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801658 | |||||||
| chr8:97801698 | C | T | 20 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0003g0073 others(17): Show |
20 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-3655C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801698 | |||||||
| chr8:97801735 | G | A | 1 | a0001c0001t0003g0114 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-3618G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801735 | |||||||
| chr8:97801749 | C | T | 20 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(17): Show |
20 | HG01081.hp2 HG01256.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-3604C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801749 | |||||||
| chr8:97801750 | G | C | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.100-3603G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801750 | |||||||
| chr8:97801780 | G | GTTGCGGT others(9): Show |
1 | a0001c0001t0027g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.100-3567_100-3552d others(18): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97801780 | ||||||
| chr8:97801792 | C | T | 6 | a0001c0001t0004g0123 a0001c0001t0004g0186 a0001c0001t0004g0219 others(3): Show |
6 | HG00609.hp2 NA18939.hp2 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-3561C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801792 | |||||||
| chr8:97801830 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.100-3523C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801830 | |||||||
| chr8:97801839 | A | G | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-3514A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801839 | |||||||
| chr8:97801843 | C | CAA | 154 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(151): Show |
154 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.100-3493_100-3492d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97801843 | ||||||
| chr8:97801843 | C | CAAA | 6 | a0001c0001t0001g0355 a0001c0001t0002g0141 a0001c0001t0002g0142 others(3): Show |
6 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-3494_100-3492d others(5): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97801843 | ||||||
| chr8:97801843 | C | CG | 9 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-3510_100-3509i others(3): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801843 | |||||||
| chr8:97801843 | CA | C | 88 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(85): Show |
88 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.100-3492delA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97801843 | ||||||
| chr8:97801843 | CAA | C | 90 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0256 others(87): Show |
90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.100-3493_100-3492d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97801843 | ||||||
| chr8:97801923 | A | C | 370 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(367): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.100-3430A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801923 | |||||||
| chr8:97801937 | T | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.100-3416T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801937 | |||||||
| chr8:97801978 | A | C | 5 | a0001c0001t0002g0360 a0001c0001t0002g0367 a0001c0001t0028g0363 others(2): Show |
5 | HG01081.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-3375A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801978 | |||||||
| chr8:97801985 | A | G | 21 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(18): Show |
21 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.100-3368A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97801985 | |||||||
| chr8:97802084 | G | T | 1 | a0001c0001t0001g0017 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.100-3269G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802084 | |||||||
| chr8:97802180 | G | A | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-3173G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802180 | |||||||
| chr8:97802262 | T | C | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-3091T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802262 | |||||||
| chr8:97802323 | A | T | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-3030A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802323 | |||||||
| chr8:97802480 | A | G | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-2873A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802480 | |||||||
| chr8:97802482 | A | G | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-2871A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802482 | |||||||
| chr8:97802489 | G | A | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.100-2864G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802489 | |||||||
| chr8:97802535 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.100-2818C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802535 | |||||||
| chr8:97802538 | C | T | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-2815C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802538 | |||||||
| chr8:97802576 | C | T | 180 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.100-2777C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802576 | |||||||
| chr8:97802593 | C | T | 1 | a0001c0001t0004g0236 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.100-2760C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802593 | |||||||
| chr8:97802605 | T | G | 1 | a0001c0001t0005g0335 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.100-2748T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802605 | |||||||
| chr8:97802742 | T | C | 169 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(166): Show |
169 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.100-2611T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802742 | |||||||
| chr8:97802817 | A | T | 1 | a0001c0001t0005g0045 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.100-2536A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802817 | |||||||
| chr8:97802818 | T | C | 1 | a0001c0001t0004g0208 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.100-2535T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802818 | |||||||
| chr8:97802864 | G | A | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.100-2489G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802864 | |||||||
| chr8:97802898 | A | G | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-2455A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802898 | |||||||
| chr8:97802899 | G | A | 8 | a0001c0001t0004g0191 a0001c0001t0004g0199 a0001c0001t0014g0172 others(5): Show |
8 | HG00099.hp1 HG00323.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-2454G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802899 | |||||||
| chr8:97802927 | A | G | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-2426A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802927 | |||||||
| chr8:97802986 | A | G | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-2367A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97802986 | |||||||
| chr8:97803072 | A | G | 38 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(35): Show |
38 | HG00733.hp1 HG00738.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.100-2281A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803072 | |||||||
| chr8:97803083 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.100-2270C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803083 | |||||||
| chr8:97803092 | G | A | 1 | a0001c0001t0008g0026 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.100-2261G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803092 | |||||||
| chr8:97803198 | C | CA | 38 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(35): Show |
38 | HG00733.hp1 HG00738.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.100-2145dupA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97803198 | ||||||
| chr8:97803198 | CA | C | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-2145delA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97803198 | ||||||
| chr8:97803387 | T | A | 1 | a0001c0001t0001g0097 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.100-1966T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803387 | |||||||
| chr8:97803424 | A | G | 2 | a0001c0001t0003g0032 a0001c0001t0003g0324 |
2 | HG03831.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.100-1929A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803424 | |||||||
| chr8:97803435 | T | C | 178 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(175): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.100-1918T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803435 | |||||||
| chr8:97803488 | G | A | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-1865G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803488 | |||||||
| chr8:97803513 | A | G | 4 | a0001c0001t0003g0148 a0001c0001t0004g0184 a0001c0001t0004g0224 others(1): Show |
4 | HG02083.hp2 NA18970.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-1840A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803513 | |||||||
| chr8:97803582 | A | G | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-1771A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803582 | |||||||
| chr8:97803594 | A | G | 20 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0003g0073 others(17): Show |
20 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-1759A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803594 | |||||||
| chr8:97803791 | A | G | 370 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(367): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.100-1562A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803791 | |||||||
| chr8:97803799 | C | T | 2 | a0001c0001t0001g0293 a0001c0001t0001g0325 |
2 | NA19060.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.100-1554C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803799 | |||||||
| chr8:97803832 | G | T | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-1521G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803832 | |||||||
| chr8:97803833 | G | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.100-1520G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803833 | |||||||
| chr8:97803971 | C | T | 121 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(118): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.100-1382C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803971 | |||||||
| chr8:97803980 | G | T | 3 | a0002c0003t0013g0190 a0002c0003t0013g0215 a0002c0003t0013g0216 |
3 | HG01515.hp2 HG01517.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.100-1373G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97803980 | |||||||
| chr8:97804039 | A | G | 16 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(13): Show |
16 | HG01081.hp2 HG01256.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-1314A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97804039 | |||||||
| chr8:97804109 | G | A | 178 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(175): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.100-1244G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97804109 | |||||||
| chr8:97804116 | G | A | 1 | a0001c0001t0036g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100-1237G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97804116 | |||||||
| chr8:97804180 | G | T | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-1173G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97804180 | |||||||
| chr8:97804272 | C | A | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-1081C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97804272 | |||||||
| chr8:97804321 | G | A | 1 | a0001c0001t0003g0285 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.100-1032G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97804321 | |||||||
| chr8:97804421 | G | A | 370 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(367): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.100-932G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97804421 | |||||||
| chr8:97804445 | G | A | 7 | a0001c0001t0001g0300 a0001c0001t0001g0320 a0001c0001t0002g0346 others(4): Show |
7 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-908G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97804445 | |||||||
| chr8:97804488 | C | G | 1 | a0001c0001t0005g0135 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.100-865C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97804488 | |||||||
| chr8:97804666 | G | T | 1 | a0001c0001t0004g0236 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.100-687G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97804666 | |||||||
| chr8:97804668 | G | A | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 others(1): Show |
4 | HG01891.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-685G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97804668 | |||||||
| chr8:97804683 | A | G | 370 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(367): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.100-670A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97804683 | |||||||
| chr8:97804710 | G | T | 1 | a0001c0001t0002g0313 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.100-643G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97804710 | |||||||
| chr8:97804792 | A | ACTGGCCT others(3): Show |
19 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0003g0073 others(16): Show |
19 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.100-541_100-532dup others(10): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97804792 | ||||||
| chr8:97804792 | ACTGGCCT others(3): Show |
A | 2 | a0001c0001t0006g0004 a0001c0001t0006g0005 |
2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.100-541_100-532del others(10): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97804792 | ||||||
| chr8:97804792 | ACTGGCCT others(8): Show |
A | 1 | a0001c0001t0002g0329 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.100-546_100-532del others(15): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97804792 | ||||||
| chr8:97805035 | G | A | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-318G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97805035 | |||||||
| chr8:97805096 | G | T | 1 | a0003c0006t0005g0034 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.100-257G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97805096 | |||||||
| chr8:97805204 | C | G | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-149C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97805204 | |||||||
| chr8:97805324 | C | CT | 52 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0001g0146 others(49): Show |
52 | HG00733.hp1 HG00735.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.100-11dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97805324 | ||||||
| chr8:97805324 | C | CTT | 137 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(134): Show |
137 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.100-12_100-11dupTT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 97805324 | ||||||
| chr8:97805331 | T | TG | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.100-22_100-21insG | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 1/6 | chr8 | 97805331 | |||||||
| chr8:97805538 | A | G | 9 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.211+74A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97805538 | |||||||
| chr8:97805568 | A | G | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.211+104A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97805568 | |||||||
| chr8:97805596 | T | C | 20 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(17): Show |
20 | HG01081.hp2 HG01256.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.211+132T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97805596 | |||||||
| chr8:97805605 | G | A | 2 | a0001c0001t0002g0121 a0001c0001t0035g0204 |
2 | HG01070.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.211+141G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97805605 | |||||||
| chr8:97805677 | T | TA | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.211+218dupA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 97805677 | ||||||
| chr8:97805826 | A | G | 1 | a0001c0001t0031g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.211+362A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97805826 | |||||||
| chr8:97805930 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.211+466G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97805930 | |||||||
| chr8:97805935 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.211+471C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97805935 | |||||||
| chr8:97805965 | A | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.211+501A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97805965 | |||||||
| chr8:97805971 | G | A | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.211+507G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97805971 | |||||||
| chr8:97806059 | A | T | 2 | a0001c0001t0003g0114 a0001c0001t0031g0030 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.211+595A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806059 | |||||||
| chr8:97806110 | A | G | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.211+646A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806110 | |||||||
| chr8:97806131 | A | G | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.211+667A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806131 | |||||||
| chr8:97806176 | G | A | 6 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0104 others(3): Show |
6 | HG00423.hp1 HG02015.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+712G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806176 | |||||||
| chr8:97806365 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.211+901C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806365 | |||||||
| chr8:97806537 | A | G | 1 | a0001c0001t0003g0324 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.211+1073A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806537 | |||||||
| chr8:97806585 | C | T | 1 | a0001c0002t0018g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.211+1121C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806585 | |||||||
| chr8:97806611 | T | C | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.211+1147T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806611 | |||||||
| chr8:97806634 | G | A | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.211+1170G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806634 | |||||||
| chr8:97806761 | A | G | 1 | a0001c0001t0010g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.211+1297A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806761 | |||||||
| chr8:97806827 | A | G | 180 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.211+1363A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806827 | |||||||
| chr8:97806838 | T | G | 1 | a0001c0004t0004g0217 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.211+1374T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806838 | |||||||
| chr8:97806858 | G | A | 3 | a0001c0001t0011g0057 a0001c0002t0019g0164 a0001c0002t0019g0246 |
3 | HG00280.hp1 HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.211+1394G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806858 | |||||||
| chr8:97806886 | T | C | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.211+1422T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806886 | |||||||
| chr8:97806906 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.211+1442C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806906 | |||||||
| chr8:97806915 | G | A | 64 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0056 others(61): Show |
64 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.211+1451G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806915 | |||||||
| chr8:97806935 | G | T | 1 | a0001c0001t0001g0294 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.211+1471G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806935 | |||||||
| chr8:97806936 | C | T | 20 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(17): Show |
20 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.211+1472C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806936 | |||||||
| chr8:97806967 | G | C | 302 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(299): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.211+1503G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97806967 | |||||||
| chr8:97807009 | A | G | 1 | a0001c0001t0003g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.211+1545A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807009 | |||||||
| chr8:97807099 | A | G | 17 | a0001c0001t0003g0013 a0001c0001t0003g0040 a0001c0001t0003g0050 others(14): Show |
17 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.211+1635A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807099 | |||||||
| chr8:97807134 | C | T | 1 | a0001c0001t0007g0178 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.211+1670C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807134 | |||||||
| chr8:97807163 | C | T | 1 | a0001c0002t0009g0251 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.211+1699C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807163 | |||||||
| chr8:97807196 | T | C | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.211+1732T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807196 | |||||||
| chr8:97807203 | T | C | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.211+1739T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807203 | |||||||
| chr8:97807205 | A | T | 21 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(18): Show |
21 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.211+1741A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807205 | |||||||
| chr8:97807267 | C | T | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.211+1803C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807267 | |||||||
| chr8:97807324 | T | G | 21 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(18): Show |
21 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.211+1860T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807324 | |||||||
| chr8:97807361 | A | C | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.211+1897A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807361 | |||||||
| chr8:97807366 | T | C | 1 | a0001c0001t0004g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.211+1902T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807366 | |||||||
| chr8:97807464 | A | G | 2 | a0001c0001t0010g0252 a0001c0001t0010g0253 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.211+2000A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807464 | |||||||
| chr8:97807634 | C | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.211+2170C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807634 | |||||||
| chr8:97807688 | A | T | 1 | a0001c0002t0009g0250 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.211+2224A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807688 | |||||||
| chr8:97807887 | T | TA | 6 | a0001c0001t0002g0142 a0001c0001t0003g0262 a0001c0001t0005g0157 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+2443dupA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 97807887 | ||||||
| chr8:97807887 | T | TAAA | 16 | a0001c0001t0003g0013 a0001c0001t0003g0040 a0001c0001t0003g0050 others(13): Show |
16 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.211+2441_211+2443d others(5): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 97807887 | ||||||
| chr8:97807887 | TAA | T | 123 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(120): Show |
123 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.211+2442_211+2443d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 97807887 | ||||||
| chr8:97807887 | TAAA | T | 28 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0003g0074 others(25): Show |
28 | HG00735.hp2 HG00741.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.211+2441_211+2443d others(5): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 97807887 | ||||||
| chr8:97807887 | TAAAAA | T | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.211+2439_211+2443d others(7): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 97807887 | ||||||
| chr8:97807964 | A | T | 40 | a0001c0001t0001g0018 a0001c0001t0001g0087 a0001c0001t0001g0136 others(37): Show |
40 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.211+2500A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807964 | |||||||
| chr8:97807967 | T | C | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.211+2503T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97807967 | |||||||
| chr8:97808086 | G | T | 2 | a0001c0001t0002g0366 a0001c0001t0002g0369 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.211+2622G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808086 | |||||||
| chr8:97808087 | C | T | 2 | a0001c0001t0002g0366 a0001c0001t0002g0369 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.211+2623C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808087 | |||||||
| chr8:97808190 | G | A | 9 | a0001c0001t0003g0059 a0001c0001t0003g0257 a0001c0001t0003g0285 others(6): Show |
9 | HG02056.hp1 NA18747.hp2 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+2726G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808190 | |||||||
| chr8:97808251 | T | C | 316 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(313): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.211+2787T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808251 | |||||||
| chr8:97808278 | A | G | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.211+2814A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808278 | |||||||
| chr8:97808377 | G | C | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.211+2913G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808377 | |||||||
| chr8:97808404 | C | T | 7 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0086 others(4): Show |
7 | HG01123.hp2 HG01192.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+2940C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808404 | |||||||
| chr8:97808463 | T | TAAAA | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.211+2999_211+3000i others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808463 | |||||||
| chr8:97808471 | T | C | 9 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(6): Show |
9 | HG01081.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.211+3007T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808471 | |||||||
| chr8:97808503 | A | G | 34 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0358 others(31): Show |
34 | HG00733.hp1 HG00738.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.211+3039A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808503 | |||||||
| chr8:97808680 | G | A | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.211+3216G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808680 | |||||||
| chr8:97808723 | C | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.211+3259C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808723 | |||||||
| chr8:97808819 | G | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.211+3355G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808819 | |||||||
| chr8:97808832 | G | A | 21 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(18): Show |
21 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.211+3368G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808832 | |||||||
| chr8:97808972 | G | A | 337 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(334): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.211+3508G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97808972 | |||||||
| chr8:97809007 | C | T | 1 | a0001c0002t0015g0167 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.211+3543C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97809007 | |||||||
| chr8:97809297 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.211+3833C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97809297 | |||||||
| chr8:97809366 | G | A | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.211+3902G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97809366 | |||||||
| chr8:97809418 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.211+3954G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97809418 | |||||||
| chr8:97809481 | C | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.211+4017C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97809481 | |||||||
| chr8:97809492 | G | A | 1 | a0001c0004t0012g0218 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.211+4028G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97809492 | |||||||
| chr8:97809537 | C | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.211+4073C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97809537 | |||||||
| chr8:97809557 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211+4093G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97809557 | |||||||
| chr8:97809780 | A | C | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.211+4316A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97809780 | |||||||
| chr8:97809831 | C | A | 1 | a0001c0001t0002g0338 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.211+4367C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97809831 | |||||||
| chr8:97809982 | G | A | 349 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(346): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.211+4518G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97809982 | |||||||
| chr8:97809994 | A | G | 1 | a0001c0001t0022g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.211+4530A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97809994 | |||||||
| chr8:97810007 | G | A | 6 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0003g0075 others(3): Show |
6 | HG00735.hp2 HG00741.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.211+4543G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97810007 | |||||||
| chr8:97810165 | G | A | 8 | a0001c0001t0002g0003 a0001c0001t0005g0006 a0001c0001t0006g0004 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.211+4701G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97810165 | |||||||
| chr8:97810337 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.211+4873G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97810337 | |||||||
| chr8:97810373 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.211+4909A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97810373 | |||||||
| chr8:97810380 | G | T | 1 | a0001c0001t0011g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.211+4916G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97810380 | |||||||
| chr8:97810391 | TTAAC | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.211+4928_211+4931d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97810391 | |||||||
| chr8:97810544 | G | T | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.212-4784G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97810544 | |||||||
| chr8:97810588 | G | A | 2 | a0001c0001t0003g0114 a0001c0001t0031g0030 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.212-4740G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97810588 | |||||||
| chr8:97810593 | G | A | 12 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(9): Show |
12 | HG01081.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.212-4735G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97810593 | |||||||
| chr8:97810862 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.212-4466A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97810862 | |||||||
| chr8:97810925 | A | G | 73 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(70): Show |
73 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.212-4403A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97810925 | |||||||
| chr8:97811068 | C | T | 1 | a0001c0001t0012g0357 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.212-4260C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811068 | |||||||
| chr8:97811069 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.212-4259G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811069 | |||||||
| chr8:97811101 | T | A | 1 | a0001c0002t0018g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.212-4227T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811101 | |||||||
| chr8:97811245 | C | T | 34 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0358 others(31): Show |
34 | HG00733.hp1 HG00738.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.212-4083C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811245 | |||||||
| chr8:97811281 | C | T | 2 | a0001c0001t0003g0289 a0001c0001t0003g0343 |
2 | NA18973.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.212-4047C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811281 | |||||||
| chr8:97811312 | C | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212-4016C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811312 | |||||||
| chr8:97811324 | G | A | 34 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0358 others(31): Show |
34 | HG00733.hp1 HG00738.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.212-4004G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811324 | |||||||
| chr8:97811598 | A | G | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-3730A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811598 | |||||||
| chr8:97811621 | T | C | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-3707T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811621 | |||||||
| chr8:97811622 | G | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-3706G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811622 | |||||||
| chr8:97811737 | A | T | 1 | a0001c0001t0004g0199 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.212-3591A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811737 | |||||||
| chr8:97811949 | G | A | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-3379G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811949 | |||||||
| chr8:97811952 | C | T | 3 | a0001c0001t0001g0273 a0001c0001t0001g0298 a0001c0001t0005g0321 |
3 | NA18949.hp1 NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.212-3376C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811952 | |||||||
| chr8:97811953 | G | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212-3375G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811953 | |||||||
| chr8:97811994 | C | T | 21 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(18): Show |
21 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.212-3334C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97811994 | |||||||
| chr8:97812011 | T | G | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.212-3317T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812011 | |||||||
| chr8:97812043 | C | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-3285C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812043 | |||||||
| chr8:97812097 | C | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212-3231C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812097 | |||||||
| chr8:97812139 | C | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212-3189C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812139 | |||||||
| chr8:97812193 | A | G | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-3135A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812193 | |||||||
| chr8:97812206 | G | GT | 22 | a0001c0001t0003g0013 a0001c0001t0003g0040 a0001c0001t0003g0050 others(19): Show |
22 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.212-3112dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 97812206 | ||||||
| chr8:97812207 | T | G | 12 | a0001c0001t0001g0018 a0001c0001t0001g0353 a0001c0001t0003g0125 others(9): Show |
12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212-3121T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812207 | |||||||
| chr8:97812208 | T | G | 2 | a0001c0001t0003g0371 a0001c0001t0035g0204 |
2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.212-3120T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812208 | |||||||
| chr8:97812213 | T | G | 12 | a0001c0001t0001g0115 a0001c0001t0003g0267 a0001c0001t0003g0274 others(9): Show |
12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212-3115T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812213 | |||||||
| chr8:97812214 | T | G | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-3114T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812214 | |||||||
| chr8:97812215 | TTG | T | 176 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(173): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.212-3111_212-3110d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 97812215 | ||||||
| chr8:97812216 | TG | T | 6 | a0001c0001t0003g0059 a0001c0001t0003g0090 a0001c0001t0004g0191 others(3): Show |
6 | HG00099.hp1 HG02056.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-3111delG | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812216 | |||||||
| chr8:97812217 | G | T | 130 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(127): Show |
130 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.212-3111G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812217 | |||||||
| chr8:97812220 | G | T | 2 | a0001c0002t0009g0375 a0001c0002t0009g0377 |
2 | HG03710.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.212-3108G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812220 | |||||||
| chr8:97812225 | TTG | T | 151 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(148): Show |
151 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.212-3101_212-3100d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 97812225 | ||||||
| chr8:97812226 | TG | T | 29 | a0001c0001t0001g0275 a0001c0001t0001g0294 a0001c0001t0001g0295 others(26): Show |
29 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.212-3101delG | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812226 | |||||||
| chr8:97812227 | G | GT | 118 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(115): Show |
118 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.212-3091dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 97812227 | ||||||
| chr8:97812227 | G | T | 6 | a0001c0001t0001g0256 a0001c0001t0001g0300 a0001c0001t0003g0297 others(3): Show |
6 | HG00642.hp1 HG01261.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-3101G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812227 | |||||||
| chr8:97812250 | G | T | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.212-3078G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812250 | |||||||
| chr8:97812281 | G | C | 8 | a0001c0001t0002g0003 a0001c0001t0005g0006 a0001c0001t0006g0004 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-3047G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812281 | |||||||
| chr8:97812345 | G | A | 21 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(18): Show |
21 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.212-2983G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812345 | |||||||
| chr8:97812405 | C | G | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-2923C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812405 | |||||||
| chr8:97812544 | C | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-2784C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812544 | |||||||
| chr8:97812624 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.212-2704C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812624 | |||||||
| chr8:97812630 | T | C | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212-2698T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812630 | |||||||
| chr8:97812652 | T | C | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-2676T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812652 | |||||||
| chr8:97812735 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.212-2593A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812735 | |||||||
| chr8:97812756 | G | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-2572G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812756 | |||||||
| chr8:97812871 | G | A | 3 | a0001c0001t0012g0129 a0001c0001t0012g0130 a0001c0001t0016g0134 |
3 | HG00673.hp2 NA18964.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.212-2457G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812871 | |||||||
| chr8:97812926 | A | G | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-2402A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97812926 | |||||||
| chr8:97813006 | G | A | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-2322G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813006 | |||||||
| chr8:97813021 | C | T | 20 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0003g0073 others(17): Show |
20 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-2307C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813021 | |||||||
| chr8:97813022 | G | A | 8 | a0001c0001t0002g0003 a0001c0001t0005g0006 a0001c0001t0006g0004 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-2306G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813022 | |||||||
| chr8:97813082 | G | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-2246G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813082 | |||||||
| chr8:97813154 | G | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212-2174G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813154 | |||||||
| chr8:97813197 | C | T | 9 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(6): Show |
9 | HG01081.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.212-2131C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813197 | |||||||
| chr8:97813316 | C | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-2012C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813316 | |||||||
| chr8:97813338 | C | A | 1 | a0001c0001t0003g0296 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.212-1990C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813338 | |||||||
| chr8:97813402 | T | G | 1 | a0001c0002t0009g0248 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.212-1926T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813402 | |||||||
| chr8:97813439 | ACAGATTG others(16): Show |
A | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-1888_212-1866d others(25): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813439 | |||||||
| chr8:97813498 | G | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-1830G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813498 | |||||||
| chr8:97813620 | G | T | 132 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(129): Show |
132 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.212-1708G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813620 | |||||||
| chr8:97813634 | T | G | 1 | a0001c0001t0008g0021 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.212-1694T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813634 | |||||||
| chr8:97813710 | ATTG | A | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.212-1609_212-1607d others(5): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 97813710 | ||||||
| chr8:97813770 | G | T | 3 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0053 |
3 | HG02280.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.212-1558G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813770 | |||||||
| chr8:97813842 | A | G | 132 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(129): Show |
132 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.212-1486A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813842 | |||||||
| chr8:97813856 | C | A | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-1472C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813856 | |||||||
| chr8:97813976 | G | A | 9 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(6): Show |
9 | HG01081.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.212-1352G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97813976 | |||||||
| chr8:97814009 | C | T | 371 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(368): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.212-1319C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814009 | |||||||
| chr8:97814079 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.212-1249C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814079 | |||||||
| chr8:97814080 | G | A | 1 | a0002c0003t0013g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.212-1248G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814080 | |||||||
| chr8:97814094 | A | G | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-1234A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814094 | |||||||
| chr8:97814105 | G | A | 1 | a0001c0001t0011g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.212-1223G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814105 | |||||||
| chr8:97814170 | G | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212-1158G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814170 | |||||||
| chr8:97814185 | T | C | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.212-1143T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814185 | |||||||
| chr8:97814325 | C | G | 1 | a0001c0001t0001g0264 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.212-1003C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814325 | |||||||
| chr8:97814372 | G | A | 34 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0358 others(31): Show |
34 | HG00733.hp1 HG00738.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.212-956G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814372 | |||||||
| chr8:97814455 | C | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-873C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814455 | |||||||
| chr8:97814479 | G | A | 1 | a0001c0001t0005g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.212-849G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814479 | |||||||
| chr8:97814543 | A | G | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212-785A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814543 | |||||||
| chr8:97814549 | A | G | 80 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(77): Show |
80 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.212-779A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814549 | |||||||
| chr8:97814551 | T | G | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-777T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814551 | |||||||
| chr8:97814626 | T | G | 1 | a0001c0001t0003g0125 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.212-702T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814626 | |||||||
| chr8:97814732 | C | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212-596C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814732 | |||||||
| chr8:97814755 | G | A | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 others(1): Show |
4 | HG01891.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-573G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814755 | |||||||
| chr8:97814767 | C | CA | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-560dupA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 97814767 | ||||||
| chr8:97814851 | G | A | 2 | a0001c0001t0002g0287 a0001c0001t0002g0340 |
2 | HG00544.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.212-477G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814851 | |||||||
| chr8:97814854 | C | T | 1 | a0001c0001t0003g0334 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.212-474C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814854 | |||||||
| chr8:97814886 | G | A | 1 | a0001c0001t0029g0374 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.212-442G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814886 | |||||||
| chr8:97814901 | A | G | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-427A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814901 | |||||||
| chr8:97814981 | C | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-347C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97814981 | |||||||
| chr8:97815012 | G | A | 1 | a0001c0001t0002g0288 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.212-316G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97815012 | |||||||
| chr8:97815016 | G | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212-312G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97815016 | |||||||
| chr8:97815064 | C | T | 337 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(334): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.212-264C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97815064 | |||||||
| chr8:97815068 | A | G | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-260A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97815068 | |||||||
| chr8:97815148 | A | T | 21 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(18): Show |
21 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.212-180A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97815148 | |||||||
| chr8:97815197 | T | C | 8 | a0001c0001t0003g0084 a0001c0001t0005g0025 a0001c0001t0005g0080 others(5): Show |
8 | HG01167.hp1 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-131T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97815197 | |||||||
| chr8:97815275 | G | C | 2 | a0001c0001t0003g0114 a0001c0001t0031g0030 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.212-53G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97815275 | |||||||
| chr8:97815303 | G | A | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.212-25G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97815303 | |||||||
| chr8:97815323 | G | C | 32 | a0001c0001t0001g0018 a0001c0001t0001g0136 a0001c0001t0001g0293 others(29): Show |
32 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(29): Show |
splice_region_variant&intron_variant | LOW | c.212-5G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 2/6 | chr8 | 97815323 | |||||||
| chr8:97815408 | C | A | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
splice_region_variant&intron_variant | LOW | c.285+7C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 3/6 | chr8 | 97815408 | |||||||
| chr8:97815568 | A | AT | 19 | a0001c0001t0001g0279 a0001c0001t0003g0013 a0001c0001t0003g0040 others(16): Show |
19 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+180dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr8 | 97815568 | ||||||
| chr8:97815791 | C | T | 1 | a0001c0001t0005g0143 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.286-267C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 3/6 | chr8 | 97815791 | |||||||
| chr8:97815987 | A | ACTT | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.286-70_286-68dupCT others(1): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr8 | 97815987 | ||||||
| chr8:97816184 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02004.hp2 | splice_region_variant&intron_variant | LOW | c.408+4C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816184 | |||||||
| chr8:97816193 | C | G | 1 | a0001c0001t0003g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.408+13C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816193 | |||||||
| chr8:97816215 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.408+35T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816215 | |||||||
| chr8:97816301 | A | G | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.408+121A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816301 | |||||||
| chr8:97816304 | C | G | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.408+124C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816304 | |||||||
| chr8:97816322 | TC | T | 79 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(76): Show |
79 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.408+143delC | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816322 | |||||||
| chr8:97816323 | C | T | 104 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0256 others(101): Show |
104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.408+143C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816323 | |||||||
| chr8:97816496 | T | C | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.408+316T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816496 | |||||||
| chr8:97816516 | T | C | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.408+336T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816516 | |||||||
| chr8:97816689 | G | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.408+509G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816689 | |||||||
| chr8:97816781 | A | G | 2 | a0001c0001t0003g0289 a0001c0001t0003g0343 |
2 | NA18973.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.408+601A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816781 | |||||||
| chr8:97816828 | C | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.408+648C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816828 | |||||||
| chr8:97816920 | A | G | 2 | a0001c0001t0027g0302 a0001c0002t0009g0251 |
2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.408+740A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816920 | |||||||
| chr8:97816931 | T | G | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.408+751T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816931 | |||||||
| chr8:97816938 | TAAAA | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.408+764_408+767del others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr8 | 97816938 | ||||||
| chr8:97816956 | AAAAGAAA others(4): Show |
A | 1 | a0001c0001t0005g0160 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.408+790_408+800del others(11): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr8 | 97816956 | ||||||
| chr8:97816988 | G | A | 1 | a0001c0001t0006g0002 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.408+808G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816988 | |||||||
| chr8:97816999 | C | T | 1 | a0001c0001t0006g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.408+819C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97816999 | |||||||
| chr8:97817056 | C | T | 1 | a0003c0006t0005g0034 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.408+876C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817056 | |||||||
| chr8:97817214 | G | A | 132 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(129): Show |
132 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.408+1034G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817214 | |||||||
| chr8:97817265 | G | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.408+1085G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817265 | |||||||
| chr8:97817278 | T | C | 123 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(120): Show |
123 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.408+1098T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817278 | |||||||
| chr8:97817345 | C | T | 101 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0256 others(98): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.408+1165C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817345 | |||||||
| chr8:97817443 | TA | T | 54 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0056 others(51): Show |
54 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.408+1264delA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817443 | |||||||
| chr8:97817444 | A | C | 67 | a0001c0001t0001g0018 a0001c0001t0001g0087 a0001c0001t0001g0102 others(64): Show |
67 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.408+1264A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817444 | |||||||
| chr8:97817445 | C | CT | 114 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0097 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.408+1285dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr8 | 97817445 | ||||||
| chr8:97817446 | T | C | 54 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0056 others(51): Show |
54 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.408+1266T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817446 | |||||||
| chr8:97817473 | A | G | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.408+1293A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817473 | |||||||
| chr8:97817484 | A | G | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.408+1304A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817484 | |||||||
| chr8:97817556 | C | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.408+1376C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817556 | |||||||
| chr8:97817573 | T | C | 316 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(313): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.408+1393T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817573 | |||||||
| chr8:97817595 | C | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.408+1415C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817595 | |||||||
| chr8:97817641 | G | C | 2 | a0001c0004t0012g0218 a0001c0004t0012g0237 |
2 | HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.408+1461G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817641 | |||||||
| chr8:97817686 | A | G | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.409-1454A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817686 | |||||||
| chr8:97817759 | A | AT | 165 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(162): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.409-1371dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr8 | 97817759 | ||||||
| chr8:97817759 | A | ATT | 18 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0002g0117 others(15): Show |
18 | HG00280.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.409-1372_409-1371d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr8 | 97817759 | ||||||
| chr8:97817870 | G | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.409-1270G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817870 | |||||||
| chr8:97817923 | T | C | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.409-1217T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817923 | |||||||
| chr8:97817995 | T | G | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.409-1145T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97817995 | |||||||
| chr8:97818195 | A | G | 1 | a0001c0001t0008g0028 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.409-945A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97818195 | |||||||
| chr8:97818204 | G | A | 1 | a0001c0001t0008g0028 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.409-936G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97818204 | |||||||
| chr8:97818358 | G | GA | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.409-782_409-781ins others(1): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97818358 | |||||||
| chr8:97818426 | C | T | 1 | a0001c0001t0002g0312 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.409-714C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97818426 | |||||||
| chr8:97818451 | C | T | 371 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(368): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.409-689C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97818451 | |||||||
| chr8:97818520 | T | C | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.409-620T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97818520 | |||||||
| chr8:97818690 | T | C | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.409-450T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97818690 | |||||||
| chr8:97818729 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.409-411G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97818729 | |||||||
| chr8:97818768 | C | T | 7 | a0001c0001t0001g0105 a0001c0001t0001g0147 a0001c0001t0002g0149 others(4): Show |
7 | HG00673.hp1 HG02027.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.409-372C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97818768 | |||||||
| chr8:97818870 | G | GA | 150 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(147): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.409-254dupA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr8 | 97818870 | ||||||
| chr8:97818957 | C | A | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.409-183C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 4/6 | chr8 | 97818957 | |||||||
| chr8:97819258 | T | G | 1 | a0001c0001t0001g0295 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.507+20T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819258 | |||||||
| chr8:97819349 | G | A | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.507+111G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819349 | |||||||
| chr8:97819373 | A | G | 1 | a0001c0001t0004g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.507+135A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819373 | |||||||
| chr8:97819624 | TTGA | T | 89 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0256 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.507+390_507+392del others(3): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97819624 | ||||||
| chr8:97819627 | A | T | 95 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(92): Show |
95 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+389A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819627 | |||||||
| chr8:97819670 | T | C | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.507+432T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819670 | |||||||
| chr8:97819727 | CT | C | 32 | a0001c0001t0001g0275 a0001c0001t0001g0300 a0001c0001t0001g0350 others(29): Show |
32 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.507+514delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97819727 | ||||||
| chr8:97819727 | CTT | C | 92 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(89): Show |
92 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.507+513_507+514del others(2): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97819727 | ||||||
| chr8:97819727 | CTTT | C | 18 | a0001c0001t0001g0101 a0001c0001t0002g0009 a0001c0001t0002g0067 others(15): Show |
18 | HG01167.hp1 HG01981.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.507+512_507+514del others(3): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97819727 | ||||||
| chr8:97819727 | CTTTT | C | 77 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(74): Show |
77 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.507+511_507+514del others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97819727 | ||||||
| chr8:97819727 | CTTTTTT | C | 119 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(116): Show |
119 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.507+509_507+514del others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97819727 | ||||||
| chr8:97819727 | CTTTTTTT | C | 9 | a0001c0001t0003g0069 a0001c0001t0003g0071 a0001c0001t0004g0181 others(6): Show |
9 | HG01169.hp1 HG01261.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.507+508_507+514del others(7): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97819727 | ||||||
| chr8:97819727 | CTTTTTTT others(1): Show |
C | 17 | a0001c0001t0003g0013 a0001c0001t0003g0040 a0001c0001t0003g0050 others(14): Show |
17 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.507+507_507+514del others(8): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97819727 | ||||||
| chr8:97819773 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.507+535C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819773 | |||||||
| chr8:97819817 | C | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.507+579C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819817 | |||||||
| chr8:97819836 | G | A | 12 | a0001c0001t0002g0358 a0001c0001t0002g0359 a0001c0001t0002g0360 others(9): Show |
12 | HG01081.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.507+598G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819836 | |||||||
| chr8:97819842 | A | C | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.507+604A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819842 | |||||||
| chr8:97819847 | G | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | HG02027.hp1 HG02523.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+609G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819847 | |||||||
| chr8:97819925 | T | C | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.507+687T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819925 | |||||||
| chr8:97819957 | G | A | 5 | a0001c0001t0001g0051 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | HG02027.hp1 NA18970.hp1 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+719G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819957 | |||||||
| chr8:97819977 | C | T | 1 | a0001c0001t0004g0184 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.507+739C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819977 | |||||||
| chr8:97819986 | C | T | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.507+748C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97819986 | |||||||
| chr8:97820007 | A | G | 185 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.507+769A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820007 | |||||||
| chr8:97820101 | T | C | 185 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.507+863T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820101 | |||||||
| chr8:97820103 | C | T | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.507+865C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820103 | |||||||
| chr8:97820161 | G | A | 185 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.507+923G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820161 | |||||||
| chr8:97820292 | T | TTTTC | 4 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+1066_507+1069d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97820292 | ||||||
| chr8:97820304 | C | CT | 9 | a0001c0001t0002g0261 a0001c0001t0002g0283 a0001c0001t0002g0348 others(6): Show |
9 | HG00639.hp1 HG00673.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.507+1082dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97820304 | ||||||
| chr8:97820304 | C | CTTT | 6 | a0001c0001t0002g0149 a0001c0001t0002g0265 a0001c0001t0003g0076 others(3): Show |
6 | HG01167.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.507+1080_507+1082d others(5): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97820304 | ||||||
| chr8:97820304 | C | CTTTT | 163 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(160): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.507+1079_507+1082d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97820304 | ||||||
| chr8:97820304 | C | CTTTTT | 9 | a0001c0001t0001g0096 a0001c0001t0001g0273 a0001c0001t0001g0279 others(6): Show |
9 | HG00280.hp2 HG00544.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.507+1078_507+1082d others(7): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97820304 | ||||||
| chr8:97820314 | T | C | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.507+1076T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820314 | |||||||
| chr8:97820327 | G | A | 185 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.507+1089G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820327 | |||||||
| chr8:97820385 | A | T | 1 | a0001c0001t0007g0178 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.507+1147A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820385 | |||||||
| chr8:97820467 | A | G | 3 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0053 |
3 | HG02280.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.507+1229A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820467 | |||||||
| chr8:97820468 | T | C | 185 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.507+1230T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820468 | |||||||
| chr8:97820564 | A | G | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.507+1326A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820564 | |||||||
| chr8:97820726 | C | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.507+1488C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820726 | |||||||
| chr8:97820727 | G | A | 185 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.507+1489G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820727 | |||||||
| chr8:97820729 | CTTG | C | 3 | a0001c0001t0003g0069 a0001c0002t0020g0376 a0001c0002t0020g0379 |
3 | HG01168.hp2 HG01169.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.507+1507_507+1509d others(5): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97820729 | ||||||
| chr8:97820781 | T | C | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.507+1543T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820781 | |||||||
| chr8:97820975 | C | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.507+1737C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820975 | |||||||
| chr8:97820997 | A | G | 370 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(367): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.507+1759A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97820997 | |||||||
| chr8:97821060 | G | A | 9 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.507+1822G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821060 | |||||||
| chr8:97821099 | A | C | 1 | a0001c0001t0002g0288 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.507+1861A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821099 | |||||||
| chr8:97821171 | A | AC | 185 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.507+1933_507+1934i others(3): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821171 | |||||||
| chr8:97821196 | C | T | 9 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.507+1958C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821196 | |||||||
| chr8:97821259 | C | T | 1 | a0001c0001t0003g0324 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.507+2021C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821259 | |||||||
| chr8:97821267 | CAG | C | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.507+2032_507+2033d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97821267 | ||||||
| chr8:97821320 | C | T | 2 | a0001c0001t0002g0261 a0001c0001t0002g0283 |
2 | HG00639.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.507+2082C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821320 | |||||||
| chr8:97821325 | C | CA | 184 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.507+2096dupA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97821325 | ||||||
| chr8:97821449 | T | C | 92 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.507+2211T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821449 | |||||||
| chr8:97821473 | C | A | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG00642.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.507+2235C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821473 | |||||||
| chr8:97821534 | C | T | 120 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(117): Show |
120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.507+2296C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821534 | |||||||
| chr8:97821538 | TGGATGTA others(23): Show |
T | 34 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0358 others(31): Show |
34 | HG00733.hp1 HG00738.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.507+2305_507+2334d others(32): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97821538 | ||||||
| chr8:97821545 | A | G | 185 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.507+2307A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821545 | |||||||
| chr8:97821601 | T | C | 185 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.507+2363T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821601 | |||||||
| chr8:97821602 | G | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.507+2364G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821602 | |||||||
| chr8:97821764 | T | G | 34 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0358 others(31): Show |
34 | HG00733.hp1 HG00738.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.507+2526T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821764 | |||||||
| chr8:97821898 | T | C | 188 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(185): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.507+2660T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821898 | |||||||
| chr8:97821921 | AT | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0319 a0001c0001t0004g0169 |
3 | NA18944.hp2 NA18982.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.507+2684delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821921 | |||||||
| chr8:97821959 | T | G | 20 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0003g0073 others(17): Show |
20 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.507+2721T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97821959 | |||||||
| chr8:97822031 | A | C | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 others(1): Show |
4 | HG01891.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+2793A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822031 | |||||||
| chr8:97822042 | C | T | 80 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(77): Show |
80 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.507+2804C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822042 | |||||||
| chr8:97822047 | G | C | 90 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(87): Show |
90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.507+2809G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822047 | |||||||
| chr8:97822081 | C | T | 1 | a0001c0001t0003g0159 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.507+2843C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822081 | |||||||
| chr8:97822222 | T | C | 1 | a0001c0001t0027g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.508-2836T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822222 | |||||||
| chr8:97822229 | AGTTC | A | 9 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-2826_508-2823d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97822229 | ||||||
| chr8:97822239 | T | C | 1 | a0001c0001t0036g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.508-2819T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822239 | |||||||
| chr8:97822391 | C | T | 2 | a0002c0003t0013g0190 a0002c0003t0013g0216 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.508-2667C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822391 | |||||||
| chr8:97822411 | TATCTTTA others(5): Show |
T | 188 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(185): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.508-2645_508-2634d others(14): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97822411 | ||||||
| chr8:97822430 | T | A | 319 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(316): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.508-2628T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822430 | |||||||
| chr8:97822435 | C | A | 21 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(18): Show |
21 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.508-2623C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822435 | |||||||
| chr8:97822452 | T | G | 21 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(18): Show |
21 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.508-2606T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822452 | |||||||
| chr8:97822501 | G | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.508-2557G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822501 | |||||||
| chr8:97822528 | T | TTTTA | 50 | a0001c0001t0001g0258 a0001c0001t0001g0264 a0001c0001t0001g0270 others(47): Show |
50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.508-2491_508-2488d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97822528 | ||||||
| chr8:97822528 | T | TTTTATTT others(9): Show |
1 | a0001c0001t0005g0144 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.508-2521_508-2520i others(18): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97822528 | ||||||
| chr8:97822528 | TTTTA | T | 87 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0056 others(84): Show |
87 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.508-2491_508-2488d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97822528 | ||||||
| chr8:97822528 | TTTTATTT others(1): Show |
T | 20 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0003g0073 others(17): Show |
20 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.508-2495_508-2488d others(10): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97822528 | ||||||
| chr8:97822528 | TTTTATTT others(13): Show |
T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.508-2507_508-2488d others(22): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97822528 | ||||||
| chr8:97822530 | T | TTATTTAT others(1): Show |
19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(16): Show |
19 | HG01433.hp1 HG01496.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.508-2521_508-2520i others(10): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97822530 | ||||||
| chr8:97822534 | T | TTATG | 42 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0060 others(39): Show |
42 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.508-2521_508-2520i others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97822534 | ||||||
| chr8:97822534 | T | TTATGTAT others(5): Show |
4 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0306 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-2521_508-2520i others(14): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97822534 | ||||||
| chr8:97822538 | T | G | 13 | a0001c0001t0001g0101 a0001c0001t0001g0273 a0001c0001t0001g0298 others(10): Show |
13 | HG01167.hp1 HG01981.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.508-2520T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822538 | |||||||
| chr8:97822571 | A | T | 5 | a0001c0001t0001g0273 a0001c0001t0001g0279 a0001c0001t0001g0291 others(2): Show |
5 | NA18949.hp1 NA18954.hp2 NA19082.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-2487A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822571 | |||||||
| chr8:97822577 | C | T | 1 | a0001c0001t0003g0315 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.508-2481C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822577 | |||||||
| chr8:97822759 | T | C | 1 | a0001c0001t0025g0292 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.508-2299T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822759 | |||||||
| chr8:97822831 | T | C | 1 | a0001c0002t0018g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.508-2227T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822831 | |||||||
| chr8:97822837 | A | ATT | 187 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(184): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.508-2214_508-2213d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97822837 | ||||||
| chr8:97822924 | C | T | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 others(1): Show |
4 | HG01891.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-2134C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822924 | |||||||
| chr8:97822961 | C | T | 1 | a0001c0001t0003g0334 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.508-2097C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822961 | |||||||
| chr8:97822998 | T | C | 149 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(146): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.508-2060T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97822998 | |||||||
| chr8:97823003 | G | T | 17 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0003g0073 others(14): Show |
17 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.508-2055G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823003 | |||||||
| chr8:97823044 | C | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.508-2014C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823044 | |||||||
| chr8:97823130 | A | C | 133 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(130): Show |
133 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.508-1928A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823130 | |||||||
| chr8:97823231 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.508-1827C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823231 | |||||||
| chr8:97823259 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.508-1799G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823259 | |||||||
| chr8:97823265 | G | A | 181 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.508-1793G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823265 | |||||||
| chr8:97823270 | C | T | 1 | a0001c0001t0003g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.508-1788C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823270 | |||||||
| chr8:97823321 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.508-1737G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823321 | |||||||
| chr8:97823322 | A | G | 1 | a0001c0001t0004g0197 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.508-1736A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823322 | |||||||
| chr8:97823344 | G | GT | 42 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0001g0115 others(39): Show |
42 | HG00609.hp1 HG00621.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.508-1703dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97823344 | ||||||
| chr8:97823349 | TTTTTTTG | T | 6 | a0001c0001t0001g0273 a0001c0001t0001g0279 a0001c0001t0001g0291 others(3): Show |
6 | HG00544.hp2 NA18949.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.508-1702_508-1696d others(9): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97823349 | ||||||
| chr8:97823352 | TTTTG | T | 108 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(105): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.508-1702_508-1699d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97823352 | ||||||
| chr8:97823354 | T | G | 66 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(63): Show |
66 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.508-1704T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823354 | |||||||
| chr8:97823355 | TG | T | 73 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(70): Show |
73 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.508-1702delG | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823355 | |||||||
| chr8:97823356 | G | GT | 29 | a0001c0001t0002g0038 a0001c0001t0002g0042 a0001c0001t0002g0079 others(26): Show |
29 | HG01081.hp2 HG02257.hp1 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.508-1692dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97823356 | ||||||
| chr8:97823356 | G | T | 128 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(125): Show |
128 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.508-1702G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823356 | |||||||
| chr8:97823358 | T | G | 111 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0078 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.508-1700T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823358 | |||||||
| chr8:97823361 | T | G | 74 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(71): Show |
74 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.508-1697T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823361 | |||||||
| chr8:97823364 | T | G | 175 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(172): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.508-1694T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823364 | |||||||
| chr8:97823367 | G | T | 184 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(181): Show |
184 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.508-1691G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823367 | |||||||
| chr8:97823370 | G | T | 150 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(147): Show |
150 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.508-1688G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823370 | |||||||
| chr8:97823373 | G | T | 7 | a0001c0001t0003g0278 a0001c0001t0005g0010 a0001c0001t0005g0036 others(4): Show |
7 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.508-1685G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823373 | |||||||
| chr8:97823388 | T | G | 312 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(309): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.508-1670T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823388 | |||||||
| chr8:97823397 | C | T | 1 | a0001c0001t0003g0110 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.508-1661C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823397 | |||||||
| chr8:97823536 | G | A | 1 | a0001c0001t0002g0287 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.508-1522G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823536 | |||||||
| chr8:97823576 | T | C | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.508-1482T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823576 | |||||||
| chr8:97823612 | T | C | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.508-1446T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823612 | |||||||
| chr8:97823694 | T | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0317 |
2 | NA18947.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.508-1364T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823694 | |||||||
| chr8:97823698 | GT | G | 58 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(55): Show |
58 | HG00733.hp1 HG00735.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.508-1345delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 97823698 | ||||||
| chr8:97823712 | TTC | T | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.508-1345_508-1344d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823712 | |||||||
| chr8:97823713 | TC | T | 16 | a0001c0001t0001g0279 a0001c0001t0002g0338 a0001c0001t0003g0278 others(13): Show |
16 | HG01099.hp1 HG01099.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.508-1344delC | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823713 | |||||||
| chr8:97823714 | C | T | 116 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(113): Show |
116 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.508-1344C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823714 | |||||||
| chr8:97823715 | G | T | 1 | a0001c0001t0006g0002 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.508-1343G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823715 | |||||||
| chr8:97823778 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.508-1280A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97823778 | |||||||
| chr8:97824155 | A | G | 4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 others(1): Show |
4 | HG01891.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-903A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97824155 | |||||||
| chr8:97824172 | G | T | 1 | a0001c0001t0002g0336 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.508-886G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97824172 | |||||||
| chr8:97824341 | A | G | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.508-717A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97824341 | |||||||
| chr8:97824418 | C | T | 1 | a0001c0001t0004g0012 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.508-640C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97824418 | |||||||
| chr8:97824421 | G | A | 121 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(118): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.508-637G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97824421 | |||||||
| chr8:97824519 | G | A | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.508-539G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97824519 | |||||||
| chr8:97824525 | G | A | 1 | a0001c0001t0016g0352 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.508-533G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97824525 | |||||||
| chr8:97824620 | G | A | 8 | a0001c0001t0003g0084 a0001c0001t0005g0025 a0001c0001t0005g0080 others(5): Show |
8 | HG01167.hp1 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.508-438G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97824620 | |||||||
| chr8:97824690 | A | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.508-368A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97824690 | |||||||
| chr8:97824772 | A | G | 181 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.508-286A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97824772 | |||||||
| chr8:97824809 | A | C | 181 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.508-249A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97824809 | |||||||
| chr8:97824833 | C | T | 1 | a0001c0001t0011g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.508-225C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97824833 | |||||||
| chr8:97824876 | C | T | 4 | a0001c0001t0012g0129 a0001c0001t0012g0130 a0001c0001t0012g0357 others(1): Show |
4 | HG00673.hp2 NA18964.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-182C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 5/6 | chr8 | 97824876 | |||||||
| chr8:97825172 | A | T | 1 | a0001c0001t0007g0182 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.603+19A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825172 | |||||||
| chr8:97825257 | A | G | 1 | a0001c0001t0006g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.603+104A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825257 | |||||||
| chr8:97825292 | C | T | 63 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(60): Show |
63 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.603+139C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825292 | |||||||
| chr8:97825396 | A | G | 2 | a0001c0001t0006g0127 a0002c0003t0005g0126 |
2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.603+243A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825396 | |||||||
| chr8:97825412 | A | G | 2 | a0001c0001t0006g0004 a0001c0001t0006g0005 |
2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.603+259A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825412 | |||||||
| chr8:97825463 | G | A | 2 | a0001c0001t0007g0195 a0001c0001t0007g0228 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.603+310G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825463 | |||||||
| chr8:97825497 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.603+344G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825497 | |||||||
| chr8:97825634 | T | C | 1 | a0001c0001t0003g0297 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.603+481T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825634 | |||||||
| chr8:97825810 | G | A | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.603+657G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825810 | |||||||
| chr8:97825814 | C | G | 14 | a0001c0001t0002g0038 a0001c0001t0002g0042 a0001c0001t0002g0079 others(11): Show |
14 | HG01081.hp2 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.603+661C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825814 | |||||||
| chr8:97825832 | A | T | 4 | a0001c0001t0003g0148 a0001c0001t0004g0184 a0001c0001t0004g0224 others(1): Show |
4 | HG02083.hp2 NA18970.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.603+679A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825832 | |||||||
| chr8:97825862 | T | A | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG00642.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.603+709T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825862 | |||||||
| chr8:97825944 | C | T | 181 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.603+791C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825944 | |||||||
| chr8:97825973 | C | G | 312 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(309): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.603+820C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97825973 | |||||||
| chr8:97826022 | G | A | 8 | a0001c0001t0002g0003 a0001c0001t0005g0006 a0001c0001t0006g0004 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.603+869G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826022 | |||||||
| chr8:97826061 | C | T | 9 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.603+908C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826061 | |||||||
| chr8:97826182 | T | C | 9 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.603+1029T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826182 | |||||||
| chr8:97826203 | T | G | 8 | a0001c0001t0002g0003 a0001c0001t0005g0006 a0001c0001t0006g0004 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.603+1050T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826203 | |||||||
| chr8:97826252 | A | G | 1 | a0001c0001t0012g0193 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.603+1099A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826252 | |||||||
| chr8:97826269 | T | G | 5 | a0001c0001t0003g0371 a0001c0001t0003g0372 a0001c0001t0003g0373 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+1116T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826269 | |||||||
| chr8:97826272 | T | C | 181 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.603+1119T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826272 | |||||||
| chr8:97826281 | A | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+1128A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826281 | |||||||
| chr8:97826360 | T | C | 130 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(127): Show |
130 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.603+1207T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826360 | |||||||
| chr8:97826436 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.603+1283C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826436 | |||||||
| chr8:97826450 | C | T | 312 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(309): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.603+1297C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826450 | |||||||
| chr8:97826543 | T | TGTTTATT others(10): Show |
182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+1393_603+1394i others(19): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97826543 | ||||||
| chr8:97826611 | T | G | 1 | a0001c0001t0001g0015 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.603+1458T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826611 | |||||||
| chr8:97826658 | A | C | 1 | a0001c0002t0021g0241 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.603+1505A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826658 | |||||||
| chr8:97826727 | T | C | 14 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0003g0073 others(11): Show |
14 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.603+1574T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826727 | |||||||
| chr8:97826729 | G | A | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.603+1576G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826729 | |||||||
| chr8:97826756 | G | A | 4 | a0001c0001t0003g0257 a0001c0001t0003g0289 a0001c0001t0003g0342 others(1): Show |
4 | NA18973.hp2 NA18995.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.603+1603G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826756 | |||||||
| chr8:97826941 | G | A | 1 | a0001c0002t0015g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.603+1788G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826941 | |||||||
| chr8:97826965 | G | A | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+1812G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97826965 | |||||||
| chr8:97827231 | T | C | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+2078T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97827231 | |||||||
| chr8:97827276 | G | C | 63 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(60): Show |
63 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.603+2123G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97827276 | |||||||
| chr8:97827369 | G | A | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+2216G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97827369 | |||||||
| chr8:97827589 | G | A | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+2436G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97827589 | |||||||
| chr8:97827620 | A | G | 181 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.603+2467A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97827620 | |||||||
| chr8:97827620 | A | T | 1 | a0001c0001t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.603+2467A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97827620 | |||||||
| chr8:97827621 | T | C | 1 | a0001c0001t0004g0213 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.603+2468T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97827621 | |||||||
| chr8:97827845 | C | T | 1 | a0001c0001t0003g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.603+2692C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97827845 | |||||||
| chr8:97827846 | G | A | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+2693G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97827846 | |||||||
| chr8:97827914 | C | A | 242 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(239): Show |
242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.603+2761C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97827914 | |||||||
| chr8:97827979 | G | A | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+2826G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97827979 | |||||||
| chr8:97827997 | T | C | 3 | a0001c0001t0006g0004 a0001c0001t0006g0005 a0001c0001t0006g0365 |
3 | HG01891.hp2 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.603+2844T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97827997 | |||||||
| chr8:97828051 | G | A | 72 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(69): Show |
72 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.603+2898G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97828051 | |||||||
| chr8:97828181 | A | C | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+3028A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97828181 | |||||||
| chr8:97828208 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.603+3055G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97828208 | |||||||
| chr8:97828270 | G | A | 2 | a0001c0001t0006g0004 a0001c0001t0006g0005 |
2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.603+3117G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97828270 | |||||||
| chr8:97828406 | A | C | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+3253A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97828406 | |||||||
| chr8:97828585 | G | A | 1 | a0001c0001t0012g0130 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.603+3432G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97828585 | |||||||
| chr8:97828660 | A | C | 8 | a0001c0001t0003g0084 a0001c0001t0005g0025 a0001c0001t0005g0080 others(5): Show |
8 | HG01167.hp1 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.603+3507A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97828660 | |||||||
| chr8:97828701 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.603+3548C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97828701 | |||||||
| chr8:97828711 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.603+3558A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97828711 | |||||||
| chr8:97828826 | C | G | 2 | a0001c0001t0003g0285 a0001c0001t0003g0334 |
2 | HG02056.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.603+3673C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97828826 | |||||||
| chr8:97828833 | G | A | 180 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.603+3680G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97828833 | |||||||
| chr8:97828872 | T | C | 2 | a0001c0001t0001g0256 a0001c0001t0034g0254 |
2 | HG01261.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.603+3719T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97828872 | |||||||
| chr8:97829339 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.603+4186C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97829339 | |||||||
| chr8:97829346 | C | T | 2 | a0001c0001t0005g0255 a0001c0002t0018g0165 |
2 | HG02040.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.603+4193C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97829346 | |||||||
| chr8:97829373 | A | G | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.603+4220A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97829373 | |||||||
| chr8:97829423 | T | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+4270T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97829423 | |||||||
| chr8:97829481 | C | T | 1 | a0001c0001t0003g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.603+4328C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97829481 | |||||||
| chr8:97829546 | G | A | 63 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(60): Show |
63 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.603+4393G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97829546 | |||||||
| chr8:97829598 | G | C | 1 | a0001c0002t0009g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.603+4445G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97829598 | |||||||
| chr8:97829601 | G | A | 53 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0038 others(50): Show |
53 | HG00733.hp1 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.603+4448G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97829601 | |||||||
| chr8:97829693 | C | CT | 6 | a0001c0001t0001g0270 a0001c0001t0001g0300 a0001c0001t0002g0322 others(3): Show |
6 | HG00280.hp2 HG00642.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.603+4542dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97829693 | ||||||
| chr8:97829696 | C | T | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.603+4543C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97829696 | |||||||
| chr8:97829698 | T | G | 2 | a0001c0001t0005g0341 a0001c0001t0016g0339 |
2 | HG00423.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.603+4545T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97829698 | |||||||
| chr8:97829755 | A | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+4602A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97829755 | |||||||
| chr8:97829777 | A | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+4624A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97829777 | |||||||
| chr8:97829976 | T | C | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+4823T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97829976 | |||||||
| chr8:97830229 | A | G | 1 | a0001c0001t0002g0260 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.603+5076A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830229 | |||||||
| chr8:97830266 | G | T | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+5113G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830266 | |||||||
| chr8:97830281 | G | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.603+5128G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830281 | |||||||
| chr8:97830359 | G | T | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+5206G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830359 | |||||||
| chr8:97830379 | T | C | 1 | a0001c0001t0003g0315 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.603+5226T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830379 | |||||||
| chr8:97830448 | A | C | 1 | a0001c0001t0002g0288 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.603+5295A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830448 | |||||||
| chr8:97830458 | T | C | 1 | a0001c0001t0003g0371 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.603+5305T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830458 | |||||||
| chr8:97830461 | A | C | 1 | a0001c0001t0022g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.603+5308A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830461 | |||||||
| chr8:97830505 | G | A | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.603+5352G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830505 | |||||||
| chr8:97830555 | C | T | 181 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.603+5402C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830555 | |||||||
| chr8:97830677 | G | A | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+5524G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830677 | |||||||
| chr8:97830692 | G | A | 1 | a0001c0001t0005g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.603+5539G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830692 | |||||||
| chr8:97830711 | C | T | 4 | a0001c0001t0003g0084 a0001c0001t0005g0080 a0001c0001t0006g0119 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.603+5558C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830711 | |||||||
| chr8:97830759 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0258 a0001c0002t0015g0247 |
3 | HG01243.hp1 HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.603+5606G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830759 | |||||||
| chr8:97830794 | C | G | 1 | a0001c0001t0036g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.603+5641C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830794 | |||||||
| chr8:97830799 | C | T | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.603+5646C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830799 | |||||||
| chr8:97830866 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.603+5713G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97830866 | |||||||
| chr8:97831000 | A | G | 375 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(372): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.603+5847A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831000 | |||||||
| chr8:97831123 | G | A | 63 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0002g0009 others(60): Show |
63 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.603+5970G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831123 | |||||||
| chr8:97831161 | A | G | 9 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.603+6008A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831161 | |||||||
| chr8:97831252 | A | C | 6 | a0001c0001t0004g0181 a0001c0001t0004g0189 a0001c0001t0004g0203 others(3): Show |
6 | HG01261.hp1 HG01943.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.603+6099A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831252 | |||||||
| chr8:97831276 | C | A | 245 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(242): Show |
245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.603+6123C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831276 | |||||||
| chr8:97831369 | G | T | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+6216G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831369 | |||||||
| chr8:97831447 | A | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+6294A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831447 | |||||||
| chr8:97831533 | T | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+6380T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831533 | |||||||
| chr8:97831541 | G | A | 1 | a0001c0001t0003g0125 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.603+6388G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831541 | |||||||
| chr8:97831645 | G | A | 2 | a0001c0001t0006g0127 a0002c0003t0005g0126 |
2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.603+6492G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831645 | |||||||
| chr8:97831678 | A | G | 9 | a0001c0001t0001g0056 a0001c0001t0004g0012 a0001c0001t0004g0192 others(6): Show |
9 | NA18956.hp1 NA18960.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.603+6525A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831678 | |||||||
| chr8:97831714 | G | T | 1 | a0001c0001t0005g0335 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.603+6561G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831714 | |||||||
| chr8:97831793 | C | T | 245 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(242): Show |
245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.603+6640C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831793 | |||||||
| chr8:97831807 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.603+6654C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831807 | |||||||
| chr8:97831808 | G | A | 1 | a0001c0001t0003g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.603+6655G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831808 | |||||||
| chr8:97831827 | G | A | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+6674G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831827 | |||||||
| chr8:97831841 | T | G | 64 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0056 others(61): Show |
64 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.603+6688T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97831841 | |||||||
| chr8:97832069 | A | T | 2 | a0001c0001t0003g0308 a0001c0001t0007g0370 |
2 | HG01243.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.603+6916A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832069 | |||||||
| chr8:97832190 | G | A | 1 | a0001c0001t0006g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.603+7037G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832190 | |||||||
| chr8:97832192 | T | A | 9 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.603+7039T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832192 | |||||||
| chr8:97832276 | T | C | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+7123T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832276 | |||||||
| chr8:97832369 | C | T | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+7216C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832369 | |||||||
| chr8:97832449 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.603+7296C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832449 | |||||||
| chr8:97832477 | G | A | 1 | a0001c0001t0005g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.603+7324G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832477 | |||||||
| chr8:97832613 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.603+7460G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832613 | |||||||
| chr8:97832676 | T | TTTTTATT others(3): Show |
3 | a0001c0001t0001g0055 a0001c0001t0001g0102 a0001c0002t0015g0249 |
3 | HG03834.hp1 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.603+7543_603+7552d others(12): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97832676 | ||||||
| chr8:97832676 | T | TTTTTATT others(8): Show |
114 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0056 others(111): Show |
114 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.603+7538_603+7552d others(17): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97832676 | ||||||
| chr8:97832676 | T | TTTTTATT others(13): Show |
10 | a0001c0001t0003g0314 a0001c0001t0008g0019 a0001c0001t0008g0021 others(7): Show |
10 | HG00558.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.603+7533_603+7552d others(22): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97832676 | ||||||
| chr8:97832676 | T | TTTTTATT others(18): Show |
2 | a0001c0001t0001g0066 a0001c0001t0008g0020 |
2 | HG02523.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.603+7528_603+7552d others(27): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97832676 | ||||||
| chr8:97832690 | T | C | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+7537T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832690 | |||||||
| chr8:97832696 | A | ATTTTATT others(4): Show |
182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+7552_603+7553i others(13): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97832696 | ||||||
| chr8:97832706 | T | A | 1 | a0001c0001t0006g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.603+7553T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832706 | |||||||
| chr8:97832707 | A | T | 1 | a0001c0001t0006g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.603+7554A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832707 | |||||||
| chr8:97832768 | G | A | 7 | a0001c0001t0002g0038 a0001c0001t0002g0042 a0001c0001t0002g0079 others(4): Show |
7 | HG02257.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.603+7615G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832768 | |||||||
| chr8:97832769 | C | T | 3 | a0001c0001t0001g0300 a0001c0001t0003g0297 a0001c0001t0023g0220 |
3 | HG00280.hp2 HG00642.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.603+7616C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832769 | |||||||
| chr8:97832775 | T | C | 371 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(368): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.603+7622T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832775 | |||||||
| chr8:97832822 | G | A | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+7669G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832822 | |||||||
| chr8:97832853 | C | T | 1 | a0001c0001t0004g0184 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.603+7700C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832853 | |||||||
| chr8:97832892 | A | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+7739A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832892 | |||||||
| chr8:97832915 | A | G | 1 | a0001c0001t0034g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.603+7762A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832915 | |||||||
| chr8:97832918 | C | G | 130 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(127): Show |
130 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.603+7765C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832918 | |||||||
| chr8:97832977 | G | A | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+7824G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832977 | |||||||
| chr8:97832988 | G | A | 1 | a0001c0001t0004g0184 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.603+7835G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97832988 | |||||||
| chr8:97833017 | T | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0102 a0001c0002t0015g0249 |
3 | HG03834.hp1 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.603+7864T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833017 | |||||||
| chr8:97833091 | C | T | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.603+7938C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833091 | |||||||
| chr8:97833124 | G | A | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+7971G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833124 | |||||||
| chr8:97833151 | C | T | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+7998C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833151 | |||||||
| chr8:97833268 | A | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+8115A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833268 | |||||||
| chr8:97833285 | A | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+8132A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833285 | |||||||
| chr8:97833354 | A | C | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.603+8201A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833354 | |||||||
| chr8:97833525 | A | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+8372A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833525 | |||||||
| chr8:97833646 | G | A | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+8493G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833646 | |||||||
| chr8:97833743 | A | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+8590A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833743 | |||||||
| chr8:97833790 | C | G | 3 | a0001c0001t0003g0076 a0001c0001t0003g0114 a0001c0001t0031g0030 |
3 | HG02451.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.603+8637C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833790 | |||||||
| chr8:97833905 | A | G | 3 | a0001c0001t0003g0267 a0001c0001t0003g0274 a0001c0001t0007g0170 |
3 | NA18939.hp1 NA18942.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.603+8752A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833905 | |||||||
| chr8:97833937 | G | A | 1 | a0001c0001t0035g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.603+8784G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833937 | |||||||
| chr8:97833991 | T | C | 56 | a0001c0001t0001g0018 a0001c0001t0001g0087 a0001c0001t0001g0293 others(53): Show |
56 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.603+8838T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97833991 | |||||||
| chr8:97834032 | C | T | 7 | a0001c0001t0001g0293 a0001c0001t0001g0325 a0001c0001t0003g0032 others(4): Show |
7 | HG03831.hp2 NA18942.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.603+8879C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97834032 | |||||||
| chr8:97834144 | G | GAAAAAAA others(3): Show |
1 | a0001c0001t0002g0322 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.603+8996_603+9005d others(12): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(4): Show |
1 | a0001c0001t0001g0295 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.603+8995_603+9005d others(13): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(5): Show |
1 | a0001c0001t0005g0255 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.603+8994_603+9005d others(14): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(12): Show |
6 | a0001c0001t0001g0106 a0001c0001t0003g0084 a0001c0001t0005g0025 others(3): Show |
6 | HG01167.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.603+9005_603+9006i others(21): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(13): Show |
28 | a0001c0001t0001g0051 a0001c0001t0001g0091 a0001c0001t0001g0093 others(25): Show |
28 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.603+9005_603+9006i others(22): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(14): Show |
17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(14): Show |
17 | HG00621.hp1 HG01496.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.603+9005_603+9006i others(23): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(15): Show |
10 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0101 others(7): Show |
10 | HG01934.hp1 HG01934.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.603+9005_603+9006i others(24): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(16): Show |
17 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0092 others(14): Show |
17 | HG00673.hp1 HG01256.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.603+9005_603+9006i others(25): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(17): Show |
10 | a0001c0001t0001g0105 a0001c0001t0002g0081 a0001c0001t0002g0139 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.603+9005_603+9006i others(26): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(18): Show |
21 | a0001c0001t0001g0062 a0001c0001t0001g0270 a0001c0001t0001g0350 others(18): Show |
21 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.603+9005_603+9006i others(27): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(19): Show |
31 | a0001c0001t0001g0264 a0001c0001t0001g0320 a0001c0001t0001g0344 others(28): Show |
31 | HG00423.hp2 HG00544.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.603+9005_603+9006i others(28): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(20): Show |
9 | a0001c0001t0001g0300 a0001c0001t0002g0345 a0001c0001t0002g0368 others(6): Show |
9 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.603+9005_603+9006i others(29): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(21): Show |
4 | a0001c0001t0002g0329 a0001c0001t0002g0366 a0001c0001t0002g0369 others(1): Show |
4 | HG00280.hp2 HG02129.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.603+9005_603+9006i others(30): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(22): Show |
1 | a0001c0001t0004g0177 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.603+9005_603+9006i others(31): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(23): Show |
2 | a0001c0001t0007g0370 a0001c0001t0010g0180 |
2 | HG01243.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.603+9005_603+9006i others(32): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(24): Show |
1 | a0001c0001t0002g0326 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.603+9005_603+9006i others(33): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(25): Show |
4 | a0001c0001t0001g0136 a0001c0001t0004g0173 a0001c0001t0011g0057 others(1): Show |
4 | HG00280.hp1 HG01358.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.603+9005_603+9006i others(34): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(26): Show |
3 | a0001c0001t0001g0077 a0001c0001t0002g0346 a0001c0002t0019g0246 |
3 | HG01361.hp1 HG03492.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.603+9005_603+9006i others(35): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(27): Show |
1 | a0001c0001t0023g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.603+9005_603+9006i others(36): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(28): Show |
1 | a0001c0001t0002g0117 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.603+9005_603+9006i others(37): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(29): Show |
1 | a0001c0001t0001g0275 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.603+9005_603+9006i others(38): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(30): Show |
1 | a0001c0001t0001g0294 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.603+9005_603+9006i others(39): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(32): Show |
1 | a0001c0001t0001g0256 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.603+9005_603+9006i others(41): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(33): Show |
1 | a0001c0001t0010g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.603+9005_603+9006i others(42): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(34): Show |
1 | a0001c0001t0034g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.603+9005_603+9006i others(43): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834144 | G | GAAAAAAA others(41): Show |
1 | a0001c0001t0001g0078 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.603+9005_603+9006i others(50): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834144 | ||||||
| chr8:97834173 | G | T | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+9020G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97834173 | |||||||
| chr8:97834320 | G | A | 92 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.603+9167G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97834320 | |||||||
| chr8:97834395 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.603+9242C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97834395 | |||||||
| chr8:97834430 | A | C | 1 | a0001c0001t0001g0272 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.603+9277A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97834430 | |||||||
| chr8:97834455 | A | T | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+9302A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97834455 | |||||||
| chr8:97834483 | G | A | 2 | a0001c0001t0003g0064 a0001c0001t0003g0314 |
2 | HG00558.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.603+9330G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97834483 | |||||||
| chr8:97834547 | TTG | T | 311 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(308): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.603+9414_603+9415d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97834547 | ||||||
| chr8:97834710 | T | C | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+9557T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97834710 | |||||||
| chr8:97834734 | T | C | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+9581T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97834734 | |||||||
| chr8:97834763 | A | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+9610A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97834763 | |||||||
| chr8:97834828 | G | A | 9 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.603+9675G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97834828 | |||||||
| chr8:97834984 | C | G | 1 | a0001c0002t0009g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.603+9831C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97834984 | |||||||
| chr8:97834994 | A | G | 1 | a0001c0002t0009g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.603+9841A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97834994 | |||||||
| chr8:97835025 | T | C | 1 | a0001c0001t0005g0160 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.603+9872T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97835025 | |||||||
| chr8:97835027 | T | C | 72 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(69): Show |
72 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.603+9874T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97835027 | |||||||
| chr8:97835166 | C | A | 1 | a0001c0001t0030g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.603+10013C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97835166 | |||||||
| chr8:97835347 | A | G | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+10194A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97835347 | |||||||
| chr8:97835358 | A | G | 3 | a0001c0001t0003g0137 a0001c0001t0003g0138 a0001c0001t0003g0154 |
3 | NA18940.hp1 NA18975.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.603+10205A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97835358 | |||||||
| chr8:97835491 | A | G | 64 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(61): Show |
64 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.603+10338A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97835491 | |||||||
| chr8:97835551 | CTG | C | 3 | a0001c0001t0003g0076 a0001c0001t0003g0114 a0001c0001t0031g0030 |
3 | HG02451.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.603+10401_603+1040 others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97835551 | ||||||
| chr8:97835661 | T | C | 182 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.603+10508T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97835661 | |||||||
| chr8:97835686 | T | A | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.603+10533T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97835686 | |||||||
| chr8:97835691 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.603+10538G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97835691 | |||||||
| chr8:97835804 | T | C | 108 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(105): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.603+10651T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97835804 | |||||||
| chr8:97835882 | AGCGGGC | A | 108 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(105): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.603+10736_603+1074 others(10): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97835882 | ||||||
| chr8:97835883 | G | T | 130 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(127): Show |
130 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.603+10730G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97835883 | |||||||
| chr8:97835919 | C | G | 108 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(105): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.603+10766C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97835919 | |||||||
| chr8:97835967 | C | G | 74 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(71): Show |
74 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.603+10814C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97835967 | |||||||
| chr8:97836072 | G | C | 6 | a0001c0001t0003g0076 a0001c0001t0003g0114 a0001c0001t0006g0127 others(3): Show |
6 | HG02055.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.603+10919G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836072 | |||||||
| chr8:97836086 | T | C | 108 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(105): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.603+10933T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836086 | |||||||
| chr8:97836089 | T | C | 7 | a0001c0001t0001g0105 a0001c0001t0001g0147 a0001c0001t0002g0149 others(4): Show |
7 | HG00673.hp1 HG02027.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.603+10936T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836089 | |||||||
| chr8:97836138 | A | C | 109 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.603+10985A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836138 | |||||||
| chr8:97836193 | T | G | 1 | a0001c0001t0004g0224 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.603+11040T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836193 | |||||||
| chr8:97836207 | G | C | 109 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.603+11054G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836207 | |||||||
| chr8:97836233 | C | T | 9 | a0001c0001t0008g0019 a0001c0001t0008g0020 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.603+11080C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836233 | |||||||
| chr8:97836462 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.603+11309C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836462 | |||||||
| chr8:97836481 | A | G | 109 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.603+11328A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836481 | |||||||
| chr8:97836664 | G | A | 1 | a0001c0001t0031g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.603+11511G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836664 | |||||||
| chr8:97836681 | A | T | 109 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.603+11528A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836681 | |||||||
| chr8:97836742 | G | T | 241 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.603+11589G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836742 | |||||||
| chr8:97836789 | T | A | 109 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.603+11636T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836789 | |||||||
| chr8:97836875 | T | C | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.603+11722T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836875 | |||||||
| chr8:97836886 | A | G | 2 | a0001c0001t0006g0127 a0002c0003t0005g0126 |
2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.603+11733A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836886 | |||||||
| chr8:97836944 | A | T | 5 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0005g0157 others(2): Show |
5 | HG01891.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.603+11791A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836944 | |||||||
| chr8:97836946 | A | T | 290 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0052 others(287): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.603+11793A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97836946 | |||||||
| chr8:97837037 | A | G | 109 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.603+11884A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837037 | |||||||
| chr8:97837075 | A | G | 241 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.603+11922A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837075 | |||||||
| chr8:97837194 | A | T | 20 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0003g0073 others(17): Show |
20 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.603+12041A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837194 | |||||||
| chr8:97837195 | C | CTT | 101 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(98): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.603+12057_603+1205 others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97837195 | ||||||
| chr8:97837195 | C | CTTT | 7 | a0001c0001t0001g0264 a0001c0001t0002g0268 a0001c0001t0002g0316 others(4): Show |
7 | HG02280.hp1 HG03130.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.603+12056_603+1205 others(7): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97837195 | ||||||
| chr8:97837270 | G | T | 2 | a0001c0001t0006g0127 a0002c0003t0005g0126 |
2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.603+12117G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837270 | |||||||
| chr8:97837272 | A | G | 130 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(127): Show |
130 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.603+12119A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837272 | |||||||
| chr8:97837433 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0005g0006 |
2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.603+12280T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837433 | |||||||
| chr8:97837444 | T | C | 109 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.603+12291T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837444 | |||||||
| chr8:97837451 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.603+12298C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837451 | |||||||
| chr8:97837492 | C | T | 1 | a0002c0003t0005g0351 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.603+12339C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837492 | |||||||
| chr8:97837547 | T | G | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.603+12394T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837547 | |||||||
| chr8:97837603 | G | C | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.603+12450G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837603 | |||||||
| chr8:97837618 | A | G | 8 | a0001c0001t0002g0003 a0001c0001t0005g0006 a0001c0001t0006g0004 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.603+12465A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837618 | |||||||
| chr8:97837647 | C | T | 1 | a0001c0001t0025g0292 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.603+12494C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837647 | |||||||
| chr8:97837681 | A | G | 3 | a0001c0001t0005g0158 a0001c0001t0013g0234 a0001c0001t0013g0235 |
3 | NA18947.hp2 NA18974.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.603+12528A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837681 | |||||||
| chr8:97837699 | C | T | 109 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.603+12546C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837699 | |||||||
| chr8:97837799 | C | CT | 130 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(127): Show |
130 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.603+12647dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97837799 | ||||||
| chr8:97837850 | C | A | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.603+12697C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97837850 | |||||||
| chr8:97838073 | A | G | 1 | a0001c0001t0003g0159 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.603+12920A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838073 | |||||||
| chr8:97838102 | T | C | 115 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0098 others(112): Show |
115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.603+12949T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838102 | |||||||
| chr8:97838268 | A | T | 108 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0136 others(105): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.603+13115A>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838268 | |||||||
| chr8:97838330 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.604-13067C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838330 | |||||||
| chr8:97838400 | T | C | 1 | a0001c0002t0018g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.604-12997T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838400 | |||||||
| chr8:97838445 | T | C | 1 | a0001c0001t0007g0182 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.604-12952T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838445 | |||||||
| chr8:97838466 | A | G | 1 | a0001c0001t0002g0367 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.604-12931A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838466 | |||||||
| chr8:97838475 | G | C | 2 | a0001c0001t0003g0308 a0001c0001t0007g0370 |
2 | HG01243.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.604-12922G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838475 | |||||||
| chr8:97838485 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.604-12912C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838485 | |||||||
| chr8:97838519 | G | A | 120 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0055 others(117): Show |
120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.604-12878G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838519 | |||||||
| chr8:97838564 | C | T | 1 | a0001c0001t0006g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.604-12833C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838564 | |||||||
| chr8:97838870 | C | T | 79 | a0001c0001t0001g0087 a0001c0001t0001g0108 a0001c0001t0001g0256 others(76): Show |
79 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.604-12527C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838870 | |||||||
| chr8:97838887 | G | T | 45 | a0001c0001t0002g0009 a0001c0001t0002g0081 a0001c0001t0002g0139 others(42): Show |
45 | HG00280.hp1 HG00280.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.604-12510G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838887 | |||||||
| chr8:97838934 | G | A | 2 | a0001c0001t0002g0346 a0001c0002t0017g0240 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.604-12463G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838934 | |||||||
| chr8:97838943 | A | G | 2 | a0001c0001t0006g0041 a0001c0002t0009g0166 |
2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.604-12454A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97838943 | |||||||
| chr8:97839013 | A | G | 1 | a0001c0001t0003g0297 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.604-12384A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839013 | |||||||
| chr8:97839090 | C | G | 50 | a0001c0001t0001g0087 a0001c0001t0003g0013 a0001c0001t0003g0032 others(47): Show |
50 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.604-12307C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839090 | |||||||
| chr8:97839242 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.604-12155T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839242 | |||||||
| chr8:97839263 | C | T | 240 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(237): Show |
240 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.604-12134C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839263 | |||||||
| chr8:97839473 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.604-11924G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839473 | |||||||
| chr8:97839488 | C | T | 77 | a0001c0001t0003g0013 a0001c0001t0003g0032 a0001c0001t0003g0040 others(74): Show |
77 | HG00438.hp1 HG00558.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.604-11909C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839488 | |||||||
| chr8:97839506 | T | A | 3 | a0001c0001t0002g0277 a0001c0001t0002g0299 a0001c0001t0010g0185 |
3 | NA18612.hp2 NA18960.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.604-11891T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839506 | |||||||
| chr8:97839518 | C | T | 11 | a0001c0001t0003g0084 a0001c0001t0006g0161 a0001c0001t0008g0011 others(8): Show |
11 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.604-11879C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839518 | |||||||
| chr8:97839594 | A | C | 1 | a0001c0001t0022g0132 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.604-11803A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839594 | |||||||
| chr8:97839595 | C | T | 65 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(62): Show |
65 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.604-11802C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839595 | |||||||
| chr8:97839707 | A | C | 1 | a0001c0001t0001g0330 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.604-11690A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839707 | |||||||
| chr8:97839731 | C | T | 2 | a0001c0001t0005g0025 a0001c0001t0005g0124 |
2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.604-11666C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839731 | |||||||
| chr8:97839749 | T | C | 3 | a0001c0001t0003g0076 a0001c0001t0007g0198 a0001c0001t0031g0030 |
3 | HG02451.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.604-11648T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839749 | |||||||
| chr8:97839954 | A | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0102 a0001c0002t0015g0249 |
3 | HG03834.hp1 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.604-11443A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97839954 | |||||||
| chr8:97840297 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.604-11100C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840297 | |||||||
| chr8:97840298 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0028g0363 |
2 | HG02258.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.604-11099G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840298 | |||||||
| chr8:97840461 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.604-10936T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840461 | |||||||
| chr8:97840490 | G | A | 14 | a0001c0001t0002g0151 a0001c0001t0002g0265 a0001c0001t0002g0266 others(11): Show |
14 | HG00609.hp2 HG02129.hp1 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.604-10907G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840490 | |||||||
| chr8:97840513 | C | A | 1 | a0001c0001t0003g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.604-10884C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840513 | |||||||
| chr8:97840540 | C | T | 1 | a0001c0001t0005g0335 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.604-10857C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840540 | |||||||
| chr8:97840622 | T | TGTCA | 37 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0076 others(34): Show |
37 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.604-10773_604-1077 others(8): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97840622 | ||||||
| chr8:97840758 | G | A | 74 | a0001c0001t0003g0013 a0001c0001t0003g0032 a0001c0001t0003g0059 others(71): Show |
74 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.604-10639G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840758 | |||||||
| chr8:97840762 | G | A | 1 | a0001c0001t0004g0197 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.604-10635G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840762 | |||||||
| chr8:97840771 | T | TGCTCCTC others(33): Show |
1 | a0001c0001t0004g0191 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.604-10608_604-1056 others(44): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97840771 | ||||||
| chr8:97840773 | C | T | 2 | a0001c0005t0001g0016 a0001c0005t0001g0023 |
2 | HG00558.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.604-10624C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840773 | |||||||
| chr8:97840789 | CGGTGGGG others(33): Show |
C | 11 | a0001c0001t0005g0010 a0001c0001t0005g0035 a0001c0001t0005g0036 others(8): Show |
11 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.604-10568_604-1052 others(44): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97840789 | ||||||
| chr8:97840838 | G | A | 24 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0076 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.604-10559G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840838 | |||||||
| chr8:97840851 | C | T | 1 | a0001c0001t0010g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.604-10546C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840851 | |||||||
| chr8:97840868 | A | G | 1 | a0001c0001t0005g0045 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.604-10529A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840868 | |||||||
| chr8:97840869 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.604-10528C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840869 | |||||||
| chr8:97840870 | G | A | 2 | a0001c0001t0001g0300 a0001c0001t0004g0191 |
2 | HG00099.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.604-10527G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840870 | |||||||
| chr8:97840890 | C | T | 24 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0076 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.604-10507C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840890 | |||||||
| chr8:97840894 | T | C | 24 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0076 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.604-10503T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840894 | |||||||
| chr8:97840921 | G | A | 8 | a0001c0001t0006g0002 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.604-10476G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840921 | |||||||
| chr8:97840925 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0011g0109 a0001c0001t0035g0204 |
3 | HG00738.hp1 HG02630.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.604-10472G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840925 | |||||||
| chr8:97840937 | C | T | 1 | a0001c0002t0009g0375 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.604-10460C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840937 | |||||||
| chr8:97840960 | A | G | 24 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0076 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.604-10437A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840960 | |||||||
| chr8:97840988 | G | T | 1 | a0001c0001t0001g0350 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.604-10409G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840988 | |||||||
| chr8:97840991 | G | A | 10 | a0001c0001t0012g0129 a0001c0001t0012g0130 a0001c0001t0012g0193 others(7): Show |
10 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.604-10406G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840991 | |||||||
| chr8:97840999 | G | A | 58 | a0001c0001t0003g0013 a0001c0001t0003g0032 a0001c0001t0003g0059 others(55): Show |
58 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.604-10398G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97840999 | |||||||
| chr8:97841030 | C | T | 2 | a0001c0001t0003g0071 a0001c0002t0009g0248 |
2 | HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.604-10367C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97841030 | |||||||
| chr8:97841031 | G | A | 13 | a0001c0001t0003g0084 a0001c0001t0006g0161 a0001c0001t0008g0011 others(10): Show |
13 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.604-10366G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97841031 | |||||||
| chr8:97841033 | C | T | 24 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0076 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.604-10364C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97841033 | |||||||
| chr8:97841124 | G | A | 1 | a0001c0001t0006g0127 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.604-10273G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97841124 | |||||||
| chr8:97841153 | T | TGGGCAGA others(33): Show |
260 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(257): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.604-10216_604-1021 others(44): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97841153 | ||||||
| chr8:97841153 | T | TGGGTAGA others(33): Show |
24 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0076 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.604-10241_604-1024 others(44): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97841153 | ||||||
| chr8:97841164 | G | GCTCCTCA others(33): Show |
1 | a0001c0001t0006g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.604-10216_604-1021 others(44): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97841164 | ||||||
| chr8:97841172 | C | CTTCCCAG others(33): Show |
3 | a0001c0001t0001g0273 a0001c0001t0001g0291 a0001c0001t0001g0298 |
3 | NA18954.hp2 NA19087.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.604-10216_604-1021 others(44): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97841172 | ||||||
| chr8:97841246 | G | A | 25 | a0001c0001t0003g0040 a0001c0001t0003g0050 a0001c0001t0003g0073 others(22): Show |
25 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.604-10151G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97841246 | |||||||
| chr8:97841491 | C | T | 2 | a0001c0001t0003g0071 a0001c0002t0009g0248 |
2 | HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.604-9906C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97841491 | |||||||
| chr8:97841562 | A | G | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-9835A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97841562 | |||||||
| chr8:97841580 | A | G | 185 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(182): Show |
185 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.604-9817A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97841580 | |||||||
| chr8:97841668 | G | T | 1 | a0001c0001t0001g0105 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.604-9729G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97841668 | |||||||
| chr8:97841692 | GTGAGTTA others(667): Show |
G | 1 | a0001c0001t0027g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.604-9698_604-9025d others(2): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97841692 | ||||||
| chr8:97841729 | A | G | 3 | a0001c0001t0003g0076 a0001c0001t0007g0198 a0001c0001t0031g0030 |
3 | HG02451.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.604-9668A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97841729 | |||||||
| chr8:97841794 | G | A | 4 | a0001c0001t0006g0041 a0001c0001t0006g0082 a0001c0001t0006g0119 others(1): Show |
4 | HG02145.hp2 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.604-9603G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97841794 | |||||||
| chr8:97841917 | A | G | 186 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(183): Show |
186 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.604-9480A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97841917 | |||||||
| chr8:97842076 | A | G | 8 | a0001c0001t0006g0002 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.604-9321A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842076 | |||||||
| chr8:97842155 | A | G | 58 | a0001c0001t0003g0013 a0001c0001t0003g0032 a0001c0001t0003g0059 others(55): Show |
58 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.604-9242A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842155 | |||||||
| chr8:97842180 | A | G | 214 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(211): Show |
214 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.604-9217A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842180 | |||||||
| chr8:97842214 | T | A | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-9183T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842214 | |||||||
| chr8:97842219 | CA | C | 79 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(76): Show |
79 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.604-9174delA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97842219 | ||||||
| chr8:97842322 | T | C | 58 | a0001c0001t0003g0013 a0001c0001t0003g0032 a0001c0001t0003g0059 others(55): Show |
58 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.604-9075T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842322 | |||||||
| chr8:97842394 | C | T | 1 | a0001c0002t0015g0247 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.604-9003C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842394 | |||||||
| chr8:97842425 | C | T | 79 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(76): Show |
79 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.604-8972C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842425 | |||||||
| chr8:97842473 | G | A | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-8924G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842473 | |||||||
| chr8:97842480 | C | T | 4 | a0001c0001t0014g0174 a0001c0001t0014g0205 a0001c0001t0014g0207 others(1): Show |
4 | HG01106.hp1 HG01168.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.604-8917C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842480 | |||||||
| chr8:97842481 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.604-8916G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842481 | |||||||
| chr8:97842575 | C | G | 2 | a0001c0001t0005g0025 a0001c0001t0005g0124 |
2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.604-8822C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842575 | |||||||
| chr8:97842581 | C | T | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-8816C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842581 | |||||||
| chr8:97842594 | C | G | 4 | a0001c0001t0006g0041 a0001c0001t0006g0082 a0001c0001t0006g0119 others(1): Show |
4 | HG02145.hp2 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.604-8803C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842594 | |||||||
| chr8:97842604 | C | T | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-8793C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842604 | |||||||
| chr8:97842649 | G | C | 5 | a0001c0001t0003g0064 a0001c0001t0003g0159 a0001c0001t0003g0285 others(2): Show |
5 | HG00609.hp1 HG02027.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-8748G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842649 | |||||||
| chr8:97842667 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.604-8730C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842667 | |||||||
| chr8:97842668 | G | A | 13 | a0001c0001t0003g0084 a0001c0001t0006g0161 a0001c0001t0008g0011 others(10): Show |
13 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.604-8729G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842668 | |||||||
| chr8:97842698 | T | C | 58 | a0001c0001t0003g0013 a0001c0001t0003g0032 a0001c0001t0003g0059 others(55): Show |
58 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.604-8699T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842698 | |||||||
| chr8:97842718 | C | A | 1 | a0001c0001t0001g0015 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.604-8679C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842718 | |||||||
| chr8:97842758 | C | G | 3 | a0001c0001t0003g0076 a0001c0001t0007g0198 a0001c0001t0031g0030 |
3 | HG02451.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.604-8639C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842758 | |||||||
| chr8:97842882 | A | C | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-8515A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842882 | |||||||
| chr8:97842884 | C | CT | 80 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(77): Show |
80 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.604-8502dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97842884 | ||||||
| chr8:97842917 | C | T | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-8480C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842917 | |||||||
| chr8:97842954 | C | T | 1 | a0001c0001t0005g0341 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.604-8443C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97842954 | |||||||
| chr8:97843383 | C | T | 3 | a0001c0001t0003g0001 a0001c0001t0005g0006 a0001c0001t0005g0157 |
3 | HG02647.hp2 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.604-8014C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97843383 | |||||||
| chr8:97843388 | T | C | 292 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(289): Show |
292 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.604-8009T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97843388 | |||||||
| chr8:97843403 | G | A | 1 | a0001c0001t0002g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.604-7994G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97843403 | |||||||
| chr8:97843468 | A | G | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-7929A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97843468 | |||||||
| chr8:97843597 | C | T | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-7800C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97843597 | |||||||
| chr8:97843680 | C | T | 2 | a0001c0001t0006g0039 a0001c0001t0035g0204 |
2 | HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.604-7717C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97843680 | |||||||
| chr8:97843729 | A | G | 1 | a0001c0001t0003g0314 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.604-7668A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97843729 | |||||||
| chr8:97843780 | C | CAAAT | 36 | a0001c0001t0001g0052 a0001c0001t0001g0062 a0001c0001t0001g0087 others(33): Show |
36 | HG00099.hp1 HG00733.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.604-7584_604-7581d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97843780 | ||||||
| chr8:97843780 | C | CAAATAAA others(1): Show |
50 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(47): Show |
50 | HG00423.hp1 HG00558.hp1 HG01175.hp1 others(47): Show |
intron_variant | MODIFIER | c.604-7588_604-7581d others(10): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97843780 | ||||||
| chr8:97843780 | C | CAAATAAA others(5): Show |
18 | a0001c0001t0001g0017 a0001c0001t0001g0054 a0001c0001t0001g0060 others(15): Show |
18 | HG00544.hp2 HG01433.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.604-7592_604-7581d others(14): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97843780 | ||||||
| chr8:97843780 | C | CAAATAAA others(13): Show |
3 | a0001c0001t0001g0273 a0001c0001t0001g0291 a0001c0001t0001g0298 |
3 | NA18954.hp2 NA19087.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.604-7600_604-7581d others(22): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97843780 | ||||||
| chr8:97843780 | C | CAAATAAA others(17): Show |
1 | a0001c0001t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.604-7604_604-7581d others(26): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97843780 | ||||||
| chr8:97843780 | CAAAT | C | 76 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(73): Show |
76 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.604-7584_604-7581d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97843780 | ||||||
| chr8:97843780 | CAAATAAA others(5): Show |
C | 1 | a0001c0001t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.604-7592_604-7581d others(14): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97843780 | ||||||
| chr8:97843780 | CAAATAAA others(9): Show |
C | 81 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(78): Show |
81 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.604-7596_604-7581d others(18): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97843780 | ||||||
| chr8:97843813 | AAATC | A | 12 | a0001c0001t0003g0084 a0001c0001t0008g0011 a0001c0001t0008g0019 others(9): Show |
12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.604-7582_604-7579d others(6): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97843813 | ||||||
| chr8:97843817 | C | A | 1 | a0001c0001t0006g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.604-7580C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97843817 | |||||||
| chr8:97844095 | TG | T | 24 | a0001c0001t0003g0040 a0001c0001t0003g0050 a0001c0001t0003g0073 others(21): Show |
24 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.604-7296delG | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97844095 | ||||||
| chr8:97844117 | G | A | 79 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(76): Show |
79 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.604-7280G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844117 | |||||||
| chr8:97844162 | A | G | 293 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(290): Show |
293 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.604-7235A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844162 | |||||||
| chr8:97844210 | A | C | 83 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-7187A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844210 | |||||||
| chr8:97844219 | A | C | 2 | a0001c0001t0002g0141 a0001c0001t0002g0142 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.604-7178A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844219 | |||||||
| chr8:97844335 | G | A | 17 | a0001c0001t0005g0010 a0001c0001t0005g0035 a0001c0001t0005g0036 others(14): Show |
17 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.604-7062G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844335 | |||||||
| chr8:97844362 | G | T | 83 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-7035G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844362 | |||||||
| chr8:97844375 | A | G | 14 | a0001c0001t0002g0151 a0001c0001t0002g0265 a0001c0001t0002g0266 others(11): Show |
14 | HG00609.hp2 HG02129.hp1 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.604-7022A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844375 | |||||||
| chr8:97844471 | T | C | 83 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-6926T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844471 | |||||||
| chr8:97844557 | G | A | 83 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-6840G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844557 | |||||||
| chr8:97844648 | C | T | 1 | a0001c0001t0012g0129 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.604-6749C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844648 | |||||||
| chr8:97844658 | C | A | 1 | a0001c0001t0005g0361 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.604-6739C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844658 | |||||||
| chr8:97844698 | TC | T | 5 | a0002c0003t0005g0083 a0002c0003t0005g0351 a0002c0003t0013g0190 others(2): Show |
5 | HG01167.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-6697delC | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97844698 | ||||||
| chr8:97844748 | T | C | 292 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(289): Show |
292 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.604-6649T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844748 | |||||||
| chr8:97844783 | T | C | 290 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(287): Show |
290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.604-6614T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844783 | |||||||
| chr8:97844790 | G | T | 78 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(75): Show |
78 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.604-6607G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844790 | |||||||
| chr8:97844983 | C | T | 83 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-6414C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97844983 | |||||||
| chr8:97845021 | C | T | 2 | a0001c0001t0005g0006 a0001c0001t0005g0157 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.604-6376C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845021 | |||||||
| chr8:97845044 | A | C | 84 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(81): Show |
84 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.604-6353A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845044 | |||||||
| chr8:97845163 | G | A | 12 | a0001c0001t0003g0084 a0001c0001t0008g0011 a0001c0001t0008g0019 others(9): Show |
12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.604-6234G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845163 | |||||||
| chr8:97845195 | A | G | 83 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-6202A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845195 | |||||||
| chr8:97845325 | GT | G | 80 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(77): Show |
80 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.604-6063delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97845325 | ||||||
| chr8:97845331 | T | G | 1 | a0001c0001t0006g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.604-6066T>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845331 | |||||||
| chr8:97845346 | G | GT | 108 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(105): Show |
108 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.604-6040dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97845346 | ||||||
| chr8:97845360 | A | C | 83 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-6037A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845360 | |||||||
| chr8:97845394 | A | G | 1 | a0002c0003t0005g0126 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.604-6003A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845394 | |||||||
| chr8:97845436 | A | G | 88 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0052 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.604-5961A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845436 | |||||||
| chr8:97845465 | C | T | 59 | a0001c0001t0001g0068 a0001c0001t0003g0013 a0001c0001t0003g0032 others(56): Show |
59 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.604-5932C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845465 | |||||||
| chr8:97845518 | A | G | 1 | a0001c0001t0027g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.604-5879A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845518 | |||||||
| chr8:97845584 | T | A | 83 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-5813T>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845584 | |||||||
| chr8:97845646 | C | T | 1 | a0001c0001t0010g0202 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.604-5751C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845646 | |||||||
| chr8:97845697 | C | T | 12 | a0001c0001t0003g0084 a0001c0001t0008g0011 a0001c0001t0008g0019 others(9): Show |
12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.604-5700C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845697 | |||||||
| chr8:97845742 | A | G | 2 | a0001c0001t0006g0039 a0001c0001t0035g0204 |
2 | HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.604-5655A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845742 | |||||||
| chr8:97845751 | G | A | 100 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0052 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.604-5646G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845751 | |||||||
| chr8:97845814 | CTT | C | 83 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-5575_604-5574d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97845814 | ||||||
| chr8:97845855 | T | C | 2 | a0001c0001t0023g0209 a0001c0001t0033g0047 |
2 | HG03195.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.604-5542T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845855 | |||||||
| chr8:97845855 | T | TCC | 48 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(45): Show |
48 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.604-5535_604-5534d others(4): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97845855 | ||||||
| chr8:97845855 | T | TCCC | 19 | a0001c0001t0002g0151 a0001c0001t0002g0265 a0001c0001t0002g0269 others(16): Show |
19 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.604-5536_604-5534d others(5): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97845855 | ||||||
| chr8:97845860 | C | CT | 83 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-5537_604-5536i others(3): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845860 | |||||||
| chr8:97845864 | T | TCCACTCC others(2): Show |
6 | a0001c0001t0005g0045 a0001c0001t0005g0058 a0001c0001t0005g0144 others(3): Show |
6 | HG02083.hp1 HG03834.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.604-5533_604-5532i others(11): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845864 | |||||||
| chr8:97845868 | A | ACTCCC | 77 | a0001c0001t0001g0068 a0001c0001t0001g0300 a0001c0001t0003g0013 others(74): Show |
77 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.604-5496_604-5492d others(7): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97845868 | ||||||
| chr8:97845868 | A | ACTCCCCT others(3): Show |
84 | a0001c0001t0001g0024 a0001c0001t0001g0055 a0001c0001t0001g0056 others(81): Show |
84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.604-5501_604-5492d others(12): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97845868 | ||||||
| chr8:97845868 | A | ACTCCCCT others(8): Show |
5 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0011g0033 others(2): Show |
5 | HG00280.hp2 HG01081.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.604-5506_604-5492d others(17): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97845868 | ||||||
| chr8:97845868 | A | ACTCCCCT others(18): Show |
1 | a0001c0001t0005g0135 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.604-5516_604-5492d others(27): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97845868 | ||||||
| chr8:97845868 | A | C | 7 | a0001c0001t0005g0045 a0001c0001t0005g0058 a0001c0001t0005g0143 others(4): Show |
7 | HG02083.hp1 HG03834.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.604-5529A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845868 | |||||||
| chr8:97845868 | ACTCCC | A | 11 | a0001c0001t0001g0051 a0001c0001t0003g0114 a0001c0001t0003g0262 others(8): Show |
11 | HG02145.hp2 HG02280.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.604-5496_604-5492d others(7): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97845868 | ||||||
| chr8:97845896 | CCCCTCCC others(8): Show |
C | 1 | a0001c0001t0002g0121 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.604-5499_604-5485d others(17): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97845896 | ||||||
| chr8:97845901 | CCCCTTCC others(3): Show |
C | 8 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.604-5494_604-5485d others(12): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97845901 | ||||||
| chr8:97845906 | T | C | 70 | a0001c0001t0001g0344 a0001c0001t0002g0042 a0001c0001t0002g0067 others(67): Show |
70 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.604-5491T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845906 | |||||||
| chr8:97845911 | T | C | 72 | a0001c0001t0001g0344 a0001c0001t0002g0042 a0001c0001t0002g0067 others(69): Show |
72 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.604-5486T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845911 | |||||||
| chr8:97845942 | G | T | 1 | a0001c0001t0001g0330 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.604-5455G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845942 | |||||||
| chr8:97845974 | C | G | 5 | a0001c0001t0006g0041 a0001c0001t0006g0082 a0001c0001t0006g0118 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.604-5423C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97845974 | |||||||
| chr8:97846080 | C | G | 6 | a0001c0001t0003g0040 a0001c0001t0003g0050 a0001c0001t0003g0371 others(3): Show |
6 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.604-5317C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846080 | |||||||
| chr8:97846088 | C | T | 1 | a0001c0001t0003g0278 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.604-5309C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846088 | |||||||
| chr8:97846113 | C | T | 1 | a0001c0002t0018g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.604-5284C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846113 | |||||||
| chr8:97846144 | C | T | 2 | a0001c0001t0002g0149 a0001c0001t0002g0156 |
2 | NA18747.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.604-5253C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846144 | |||||||
| chr8:97846152 | C | T | 1 | a0001c0001t0006g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.604-5245C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846152 | |||||||
| chr8:97846159 | A | G | 83 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-5238A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846159 | |||||||
| chr8:97846327 | A | AT | 77 | a0001c0001t0001g0052 a0001c0001t0001g0097 a0001c0001t0001g0153 others(74): Show |
77 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.604-5052dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97846327 | ||||||
| chr8:97846327 | ATTT | A | 80 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(77): Show |
80 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.604-5054_604-5052d others(5): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97846327 | ||||||
| chr8:97846350 | T | C | 83 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-5047T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846350 | |||||||
| chr8:97846351 | G | A | 83 | a0001c0001t0001g0068 a0001c0001t0002g0141 a0001c0001t0002g0142 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-5046G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846351 | |||||||
| chr8:97846418 | C | T | 1 | a0001c0001t0006g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.604-4979C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846418 | |||||||
| chr8:97846441 | C | T | 1 | a0001c0001t0005g0044 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.604-4956C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846441 | |||||||
| chr8:97846479 | C | T | 1 | a0001c0001t0002g0284 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.604-4918C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846479 | |||||||
| chr8:97846541 | G | T | 1 | a0001c0001t0003g0064 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.604-4856G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846541 | |||||||
| chr8:97846573 | C | T | 3 | a0001c0001t0003g0076 a0001c0001t0007g0198 a0001c0001t0031g0030 |
3 | HG02451.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.604-4824C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846573 | |||||||
| chr8:97846757 | A | G | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-4640A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846757 | |||||||
| chr8:97846962 | A | G | 17 | a0001c0001t0005g0025 a0001c0001t0005g0045 a0001c0001t0005g0058 others(14): Show |
17 | HG00673.hp1 HG02074.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.604-4435A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97846962 | |||||||
| chr8:97847013 | A | G | 58 | a0001c0001t0003g0013 a0001c0001t0003g0032 a0001c0001t0003g0059 others(55): Show |
58 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.604-4384A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97847013 | |||||||
| chr8:97847066 | A | G | 1 | a0001c0001t0027g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.604-4331A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97847066 | |||||||
| chr8:97847209 | T | C | 175 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(172): Show |
175 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.604-4188T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97847209 | |||||||
| chr8:97847248 | G | C | 376 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(373): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.604-4149G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97847248 | |||||||
| chr8:97847355 | T | C | 10 | a0001c0001t0012g0129 a0001c0001t0012g0130 a0001c0001t0012g0193 others(7): Show |
10 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.604-4042T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97847355 | |||||||
| chr8:97847377 | G | A | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-4020G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97847377 | |||||||
| chr8:97847550 | G | A | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-3847G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97847550 | |||||||
| chr8:97847702 | T | C | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-3695T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97847702 | |||||||
| chr8:97847800 | G | A | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-3597G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97847800 | |||||||
| chr8:97847954 | G | T | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-3443G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97847954 | |||||||
| chr8:97848001 | T | C | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-3396T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97848001 | |||||||
| chr8:97848217 | G | A | 1 | a0001c0001t0006g0007 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.604-3180G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97848217 | |||||||
| chr8:97848312 | A | G | 2 | a0001c0001t0005g0025 a0001c0001t0005g0124 |
2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.604-3085A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97848312 | |||||||
| chr8:97848333 | T | C | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-3064T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97848333 | |||||||
| chr8:97848363 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.604-3034T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97848363 | |||||||
| chr8:97848404 | A | AT | 80 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(77): Show |
80 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.604-2983dupT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97848404 | ||||||
| chr8:97848437 | TCTG | T | 12 | a0001c0001t0003g0084 a0001c0001t0008g0011 a0001c0001t0008g0019 others(9): Show |
12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.604-2959_604-2957d others(5): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97848437 | |||||||
| chr8:97848441 | T | C | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-2956T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97848441 | |||||||
| chr8:97848484 | G | GA | 13 | a0001c0001t0003g0084 a0001c0001t0006g0161 a0001c0001t0008g0011 others(10): Show |
13 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.604-2904dupA | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97848484 | ||||||
| chr8:97848583 | G | T | 3 | a0001c0001t0003g0286 a0001c0001t0003g0331 a0001c0001t0032g0318 |
3 | NA18940.hp2 NA19010.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.604-2814G>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97848583 | |||||||
| chr8:97848794 | C | T | 58 | a0001c0001t0003g0013 a0001c0001t0003g0032 a0001c0001t0003g0059 others(55): Show |
58 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.604-2603C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97848794 | |||||||
| chr8:97848938 | C | T | 3 | a0001c0001t0003g0076 a0001c0001t0007g0198 a0001c0001t0031g0030 |
3 | HG02451.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.604-2459C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97848938 | |||||||
| chr8:97848955 | CT | C | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-2438delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97848955 | ||||||
| chr8:97849009 | A | G | 1 | a0001c0001t0005g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.604-2388A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849009 | |||||||
| chr8:97849127 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.604-2270C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849127 | |||||||
| chr8:97849128 | C | G | 79 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(76): Show |
79 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.604-2269C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849128 | |||||||
| chr8:97849221 | T | C | 83 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(80): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-2176T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849221 | |||||||
| chr8:97849223 | G | A | 1 | a0001c0001t0003g0296 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.604-2174G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849223 | |||||||
| chr8:97849441 | A | G | 82 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0013 others(79): Show |
82 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.604-1956A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849441 | |||||||
| chr8:97849447 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.604-1950G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849447 | |||||||
| chr8:97849497 | G | A | 1 | a0001c0001t0014g0206 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.604-1900G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849497 | |||||||
| chr8:97849552 | A | G | 1 | a0001c0001t0003g0314 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.604-1845A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849552 | |||||||
| chr8:97849616 | T | C | 111 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0100 others(108): Show |
111 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.604-1781T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849616 | |||||||
| chr8:97849664 | G | A | 1 | a0001c0001t0003g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.604-1733G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849664 | |||||||
| chr8:97849774 | T | C | 124 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0151 others(121): Show |
124 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.604-1623T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849774 | |||||||
| chr8:97849792 | A | AC | 24 | a0001c0001t0001g0087 a0001c0001t0001g0270 a0001c0001t0001g0279 others(21): Show |
24 | HG00438.hp1 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.604-1598dupC | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97849792 | ||||||
| chr8:97849792 | A | C | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.604-1605A>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849792 | |||||||
| chr8:97849793 | C | A | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.604-1604C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849793 | |||||||
| chr8:97849799 | CT | C | 5 | a0002c0003t0005g0083 a0002c0003t0005g0351 a0002c0003t0013g0190 others(2): Show |
5 | HG01167.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-1597delT | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849799 | |||||||
| chr8:97849810 | C | G | 1 | a0001c0001t0005g0145 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.604-1587C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849810 | |||||||
| chr8:97849810 | C | T | 13 | a0001c0001t0002g0042 a0001c0001t0002g0141 a0001c0001t0002g0142 others(10): Show |
13 | HG01891.hp1 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.604-1587C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849810 | |||||||
| chr8:97849826 | G | C | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.604-1571G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849826 | |||||||
| chr8:97849827 | C | A | 2 | a0001c0001t0006g0039 a0001c0001t0035g0204 |
2 | HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.604-1570C>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849827 | |||||||
| chr8:97849827 | C | G | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.604-1570C>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97849827 | |||||||
| chr8:97849837 | CTGTGTGT others(1237): Show |
C | 6 | a0001c0001t0006g0041 a0001c0001t0006g0082 a0001c0001t0006g0118 others(3): Show |
6 | HG02145.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.604-1557_604-314de others(1): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97849837 | ||||||
| chr8:97850006 | G | C | 201 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(198): Show |
201 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.604-1391G>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97850006 | |||||||
| chr8:97850013 | C | T | 89 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0001 others(86): Show |
89 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.604-1384C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97850013 | |||||||
| chr8:97850027 | A | G | 150 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(147): Show |
150 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.604-1370A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97850027 | |||||||
| chr8:97850173 | A | G | 92 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0001 others(89): Show |
92 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.604-1224A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97850173 | |||||||
| chr8:97850203 | A | G | 128 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0001 others(125): Show |
128 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(125): Show |
intron_variant | MODIFIER | c.604-1194A>G | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97850203 | |||||||
| chr8:97850322 | T | C | 112 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(109): Show |
112 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.604-1075T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97850322 | |||||||
| chr8:97850378 | C | T | 2 | a0001c0001t0005g0006 a0001c0001t0005g0157 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.604-1019C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97850378 | |||||||
| chr8:97850465 | G | GGGGTGTG others(11): Show |
6 | a0001c0001t0006g0004 a0001c0001t0006g0005 a0001c0001t0006g0007 others(3): Show |
6 | HG01891.hp2 HG02145.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.604-931_604-930ins others(18): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850465 | ||||||
| chr8:97850465 | G | GGGGTGTG others(13): Show |
1 | a0001c0001t0006g0002 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.604-931_604-930ins others(20): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850465 | ||||||
| chr8:97850465 | G | GGGGTGTG others(15): Show |
1 | a0001c0002t0018g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.604-931_604-930ins others(22): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850465 | ||||||
| chr8:97850465 | G | GGTGTGTG others(11): Show |
1 | a0001c0001t0006g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.604-925_604-908dup others(18): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850465 | ||||||
| chr8:97850474 | G | A | 8 | a0001c0001t0006g0002 a0001c0001t0006g0004 a0001c0001t0006g0005 others(5): Show |
8 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.604-923G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97850474 | |||||||
| chr8:97850474 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0003g0372 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.604-910_604-909ins others(14): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850474 | ||||||
| chr8:97850474 | G | GTGTGTGT others(9): Show |
2 | a0001c0001t0006g0039 a0001c0001t0035g0204 |
2 | HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.604-908_604-907ins others(16): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850474 | ||||||
| chr8:97850474 | G | GTGTGTGT others(11): Show |
17 | a0001c0001t0003g0040 a0001c0001t0003g0050 a0001c0001t0003g0073 others(14): Show |
17 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.604-908_604-907ins others(18): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850474 | ||||||
| chr8:97850474 | G | GTGTGTGT others(13): Show |
15 | a0001c0001t0003g0076 a0001c0001t0007g0171 a0001c0001t0007g0198 others(12): Show |
15 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.604-908_604-907ins others(20): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850474 | ||||||
| chr8:97850474 | G | GTGTGTGT others(15): Show |
58 | a0001c0001t0003g0001 a0001c0001t0003g0032 a0001c0001t0003g0059 others(55): Show |
58 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.604-908_604-907ins others(22): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850474 | ||||||
| chr8:97850474 | G | GTGTGTGT others(17): Show |
6 | a0001c0001t0003g0013 a0001c0001t0003g0114 a0001c0001t0003g0262 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.604-908_604-907ins others(24): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850474 | ||||||
| chr8:97850474 | G | GTGTGTGT others(19): Show |
1 | a0001c0001t0003g0071 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.604-908_604-907ins others(26): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850474 | ||||||
| chr8:97850476 | G | GTGTGTGT others(8): Show |
1 | a0001c0001t0013g0234 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.604-908_604-907ins others(15): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850476 | ||||||
| chr8:97850476 | G | GTGTGTGT others(9): Show |
4 | a0001c0001t0005g0143 a0001c0001t0005g0144 a0001c0001t0005g0158 others(1): Show |
4 | NA18947.hp2 NA18977.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.604-908_604-907ins others(16): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850476 | ||||||
| chr8:97850476 | G | GTGTGTGT others(25): Show |
28 | a0001c0001t0005g0006 a0001c0001t0005g0025 a0001c0001t0005g0035 others(25): Show |
28 | HG00673.hp1 HG00733.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.604-908_604-907ins others(32): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850476 | ||||||
| chr8:97850476 | G | GTGTGTGT others(11): Show |
4 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0010g0226 others(1): Show |
4 | HG00438.hp1 HG01891.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.604-908_604-907ins others(18): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850476 | ||||||
| chr8:97850476 | G | GTGTGTGT others(27): Show |
2 | a0001c0001t0005g0152 a0001c0001t0005g0255 |
2 | HG02040.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.604-908_604-907ins others(34): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850476 | ||||||
| chr8:97850476 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0002g0313 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.604-908_604-907ins others(20): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850476 | ||||||
| chr8:97850476 | G | GTGTGTGT others(15): Show |
83 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0038 others(80): Show |
83 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.604-908_604-907ins others(22): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850476 | ||||||
| chr8:97850476 | G | GTGTGTGT others(17): Show |
3 | a0001c0001t0002g0338 a0001c0001t0002g0346 a0001c0002t0017g0240 |
3 | HG01099.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.604-908_604-907ins others(24): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850476 | ||||||
| chr8:97850476 | G | GTGTGTGT others(19): Show |
2 | a0001c0001t0010g0252 a0001c0001t0010g0253 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.604-908_604-907ins others(26): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850476 | ||||||
| chr8:97850477 | T | TGTGTGTG others(26): Show |
1 | a0001c0001t0005g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.604-908_604-907ins others(33): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 97850477 | ||||||
| chr8:97850613 | C | T | 22 | a0001c0001t0006g0002 a0001c0001t0006g0004 a0001c0001t0006g0005 others(19): Show |
22 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.604-784C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97850613 | |||||||
| chr8:97850686 | G | A | 1 | a0001c0001t0006g0365 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.604-711G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97850686 | |||||||
| chr8:97850803 | G | A | 1 | a0001c0001t0006g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.604-594G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97850803 | |||||||
| chr8:97850862 | C | T | 1 | a0001c0001t0003g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.604-535C>T | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97850862 | |||||||
| chr8:97851051 | T | C | 22 | a0001c0001t0006g0002 a0001c0001t0006g0004 a0001c0001t0006g0005 others(19): Show |
22 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.604-346T>C | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97851051 | |||||||
| chr8:97851342 | G | A | 5 | a0001c0001t0006g0041 a0001c0001t0006g0082 a0001c0001t0006g0118 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.604-55G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97851342 | |||||||
| chr8:97851355 | G | A | 11 | a0001c0001t0005g0010 a0001c0001t0005g0035 a0001c0001t0005g0036 others(8): Show |
11 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.604-42G>A | LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | chr8 | 97851355 |