Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9388 |
| ensemblid | ENSG00000101670.12 |
| hgncid | 6623 |
| symbol | LIPG |
| name | lipase G, endothelial type |
| refseq_nuc | NM_006033.4 |
| refseq_prot | NP_006024.1 |
| ensembl_nuc | ENST00000261292.9 |
| ensembl_prot | ENSP00000261292.4 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 49562057 |
| end | 49599185 |
| strand | + |
| ver | v1.2 |
| region | chr18:49562057-49599185 |
| region5000 | chr18:49557057-49604185 |
| regionname0 | LIPG_chr18_49562057_49599185 |
| regionname5000 | LIPG_chr18_49557057_49604185 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 500 | 282 | 70 | 64 | 104 | 10 | 33 | 80 | LIPG_chr18_49557057_49604185 | LIPG | MSNSV others(495): Show |
chr18 | 49557057 | 49604185 |
| a0002 | 0/1 | 500 | 85 | 10 | 15 | 45 | 3 | 11 | 32 | LIPG_chr18_49557057_49604185 | LIPG | MSNSV others(495): Show |
chr18 | 49557057 | 49604185 |
| a0003 | 0/0 | 500 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | MSNSV others(495): Show |
chr18 | 49557057 | 49604185 |
| a0004 | 0/0 | 500 | 6 | 5 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | MSNSV others(495): Show |
chr18 | 49557057 | 49604185 |
| a0005 | 0/0 | 500 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | MSNSV others(495): Show |
chr18 | 49557057 | 49604185 |
| a0006 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | MSNSV others(495): Show |
chr18 | 49557057 | 49604185 |
| a0007 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | MSNSV others(495): Show |
chr18 | 49557057 | 49604185 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1500 | 264 | 54 | 62 | 104 | 10 | 33 | LIPG_chr18_49557057_49604185 | LIPG | ATGAG others(1495): Show |
chr18 | 49557057 | 49604185 | ||
| a0001c0003 | 0/0 | 1500 | 11 | 10 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | ATGAG others(1495): Show |
chr18 | 49557057 | 49604185 | ||
| a0001c0005 | 0/0 | 1500 | 6 | 5 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | ATGAG others(1495): Show |
chr18 | 49557057 | 49604185 | ||
| a0001c0011 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | ATGAG others(1495): Show |
chr18 | 49557057 | 49604185 | ||
| a0002c0002 | 0/1 | 1500 | 83 | 10 | 15 | 44 | 3 | 10 | LIPG_chr18_49557057_49604185 | LIPG | ATGAG others(1495): Show |
chr18 | 49557057 | 49604185 | ||
| a0002c0012 | 0/0 | 1500 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | ATGAG others(1495): Show |
chr18 | 49557057 | 49604185 | ||
| a0002c0013 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | ATGAG others(1495): Show |
chr18 | 49557057 | 49604185 | ||
| a0003c0004 | 0/0 | 1500 | 8 | 8 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | ATGAG others(1495): Show |
chr18 | 49557057 | 49604185 | ||
| a0004c0006 | 0/0 | 1500 | 5 | 5 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | ATGAG others(1495): Show |
chr18 | 49557057 | 49604185 | ||
| a0004c0010 | 0/0 | 1500 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | ATGAG others(1495): Show |
chr18 | 49557057 | 49604185 | ||
| a0005c0009 | 0/0 | 1500 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | ATGAG others(1495): Show |
chr18 | 49557057 | 49604185 | ||
| a0006c0008 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | ATGAG others(1495): Show |
chr18 | 49557057 | 49604185 | ||
| a0007c0007 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | ATGAG others(1495): Show |
chr18 | 49557057 | 49604185 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 10419 | 37 | 6 | 6 | 19 | 2 | 4 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0002 | 0/0 | 10419 | 30 | 0 | 2 | 22 | 0 | 6 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0003 | 0/0 | 10418 | 25 | 7 | 3 | 11 | 0 | 4 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0006 | 0/0 | 10418 | 11 | 0 | 4 | 5 | 1 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0008 | 0/0 | 10419 | 9 | 0 | 7 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0010 | 0/0 | 10418 | 7 | 0 | 2 | 0 | 1 | 4 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0011 | 0/0 | 10419 | 8 | 0 | 7 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0012 | 1/0 | 10418 | 8 | 0 | 2 | 0 | 2 | 3 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0013 | 0/0 | 10418 | 6 | 0 | 2 | 4 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0015 | 0/0 | 10419 | 6 | 0 | 6 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0017 | 0/0 | 10417 | 4 | 4 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10412): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0018 | 0/0 | 10420 | 3 | 0 | 0 | 2 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0019 | 0/0 | 10420 | 4 | 0 | 0 | 3 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0020 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0024 | 0/0 | 10417 | 3 | 3 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10412): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0025 | 0/0 | 10419 | 3 | 0 | 0 | 3 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0026 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0027 | 0/0 | 10418 | 3 | 0 | 1 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0032 | 0/0 | 10418 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0033 | 0/0 | 10417 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10412): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0034 | 0/0 | 10418 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0035 | 0/0 | 10419 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0036 | 0/0 | 10418 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0037 | 0/0 | 10420 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0038 | 0/0 | 10429 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10424): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0039 | 0/0 | 10417 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10412): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0040 | 0/0 | 10417 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10412): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0041 | 0/0 | 10420 | 2 | 1 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0042 | 0/0 | 10419 | 2 | 0 | 0 | 0 | 0 | 2 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0043 | 0/0 | 10419 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0044 | 0/0 | 10419 | 2 | 1 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0046 | 0/0 | 10419 | 2 | 0 | 1 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0047 | 0/0 | 10418 | 2 | 0 | 0 | 1 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0048 | 0/0 | 10421 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10416): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0049 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0052 | 0/0 | 10419 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0053 | 0/0 | 10418 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0055 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0056 | 0/0 | 10418 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0061 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0076 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0077 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0078 | 0/0 | 10416 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10411): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0079 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0081 | 0/0 | 10421 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10416): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0082 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0083 | 0/0 | 10417 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10412): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0084 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0085 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0086 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0089 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0090 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0091 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0092 | 0/0 | 10420 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0093 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0094 | 0/0 | 10428 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10423): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0095 | 0/0 | 10430 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10425): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0096 | 0/0 | 10430 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10425): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0097 | 0/0 | 10417 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10412): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0098 | 0/0 | 10427 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10422): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0101 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0102 | 0/0 | 10417 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10412): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0104 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0105 | 0/0 | 10417 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10412): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0106 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0107 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0108 | 0/0 | 10417 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10412): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0110 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0111 | 0/0 | 10417 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10412): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0112 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0113 | 0/0 | 10418 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0114 | 0/0 | 10418 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0115 | 0/0 | 10417 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10412): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0116 | 0/0 | 10417 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10412): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0117 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0119 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0120 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0122 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0123 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0124 | 0/0 | 10419 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0125 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0126 | 0/0 | 10420 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0127 | 0/0 | 10420 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0128 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0129 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0131 | 0/0 | 10419 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0132 | 0/0 | 10419 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0133 | 0/0 | 10418 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0134 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0135 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0136 | 0/0 | 10419 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0137 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0138 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0139 | 0/0 | 10437 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10432): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0140 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0141 | 0/0 | 10433 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10428): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0142 | 0/0 | 10419 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0001t0143 | 0/0 | 10421 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10416): Show |
chr18 | 49557057 | 49604185 |
| a0001c0003t0007 | 0/0 | 10419 | 6 | 5 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0003t0045 | 0/0 | 10420 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0003t0099 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0003t0118 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0001c0003t0121 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0005t0007 | 0/0 | 10419 | 4 | 4 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0001c0005t0100 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0005t0103 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0001c0011t0068 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0004 | 0/0 | 10420 | 16 | 0 | 0 | 16 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0005 | 0/0 | 10419 | 15 | 1 | 6 | 4 | 1 | 3 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0009 | 0/0 | 10419 | 9 | 1 | 2 | 4 | 2 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0014 | 0/0 | 10420 | 6 | 6 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0018 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0020 | 0/0 | 10418 | 2 | 0 | 0 | 0 | 0 | 2 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0021 | 0/0 | 10419 | 3 | 0 | 2 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0022 | 0/0 | 10420 | 3 | 0 | 0 | 3 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0023 | 0/0 | 10421 | 3 | 0 | 0 | 3 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10416): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0028 | 0/0 | 10420 | 2 | 0 | 1 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0030 | 0/0 | 10421 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10416): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0031 | 0/0 | 10419 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0050 | 0/0 | 10421 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10416): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0051 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0054 | 0/0 | 10419 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0058 | 0/0 | 10418 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0059 | 0/0 | 10419 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0060 | 0/0 | 10420 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0062 | 0/0 | 10421 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10416): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0063 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0064 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0065 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0066 | 0/0 | 10421 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10416): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0067 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0069 | 0/0 | 10422 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10417): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0070 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0071 | 0/0 | 10407 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10402): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0072 | 0/0 | 10420 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0073 | 0/0 | 10420 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0074 | 0/1 | 10420 | 1 | 0 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0002c0002t0130 | 0/0 | 10421 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10416): Show |
chr18 | 49557057 | 49604185 |
| a0002c0012t0057 | 0/0 | 10419 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0002c0013t0004 | 0/0 | 10420 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0003c0004t0016 | 0/0 | 10412 | 5 | 5 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10407): Show |
chr18 | 49557057 | 49604185 |
| a0003c0004t0026 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0003c0004t0080 | 0/0 | 10412 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10407): Show |
chr18 | 49557057 | 49604185 |
| a0003c0004t0109 | 0/0 | 10419 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0004c0006t0029 | 0/0 | 10419 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0004c0006t0075 | 0/0 | 10418 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0004c0006t0087 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| a0004c0006t0088 | 0/0 | 10421 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10416): Show |
chr18 | 49557057 | 49604185 |
| a0004c0010t0010 | 0/0 | 10418 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0005c0009t0013 | 0/0 | 10418 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10413): Show |
chr18 | 49557057 | 49604185 |
| a0006c0008t0008 | 0/0 | 10419 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10414): Show |
chr18 | 49557057 | 49604185 |
| a0007c0007t0026 | 0/0 | 10420 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | AGCAG others(10415): Show |
chr18 | 49557057 | 49604185 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0006g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0006g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0008g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0008g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0008g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0008g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0008g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0008g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0008g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0008g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0010g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0010g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0010g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0010g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0010g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0010g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0010g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0011g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0011g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0011g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0011g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0011g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0011g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0011g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0012g0003 | 1/0 | 3 | 0 | 1 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0012g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0012g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0012g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0012g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0012g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0013g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0013g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0013g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0013g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0013g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0013g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0015g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0015g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0015g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0015g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0015g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0017g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0017g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0017g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0017g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0018g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0018g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0018g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0019g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0019g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0019g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0019g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0020g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0024g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0024g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0025g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0025g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0025g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0026g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0027g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0027g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0027g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0032g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0032g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0033g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0033g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0034g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0034g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0035g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0035g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0036g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0036g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0037g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0037g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0038g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0038g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0039g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0039g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0040g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0040g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0041g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0041g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0042g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0043g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0043g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0044g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0044g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0046g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0046g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0047g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0047g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0048g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0049g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0052g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0053g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0055g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0056g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0061g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0076g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0077g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0078g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0079g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0081g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0082g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0083g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0084g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0085g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0086g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0089g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0090g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0091g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0092g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0093g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0094g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0095g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0096g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0097g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0098g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0101g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0102g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0104g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0105g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0106g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0107g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0108g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0110g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0111g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0112g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0113g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0114g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0115g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0116g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0117g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0119g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0120g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0122g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0123g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0124g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0125g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0126g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0127g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0128g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0129g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0131g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0132g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0133g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0134g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0135g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0136g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0137g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0138g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0139g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0140g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0141g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0142g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0001t0143g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0003t0007g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0003t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0003t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0003t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0003t0007g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0003t0045g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0003t0045g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0003t0099g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0003t0118g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0003t0121g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0005t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0005t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0005t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0005t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0005t0100g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0005t0103g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0001c0011t0068g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0005g0001 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0005g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0005g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0005g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0005g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0005g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0005g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0009g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0009g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0009g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0009g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0009g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0009g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0009g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0009g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0014g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0014g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0014g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0014g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0014g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0018g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0020g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0020g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0021g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0021g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0022g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0022g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0022g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0023g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0023g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0023g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0028g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0028g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0030g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0030g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0031g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0050g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0051g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0054g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0058g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0059g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0060g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0062g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0063g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0064g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0065g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0066g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0067g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0069g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0070g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0071g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0072g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0073g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0074g0346 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0002t0130g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0012t0057g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0002c0013t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0003c0004t0016g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0003c0004t0016g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0003c0004t0016g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0003c0004t0016g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0003c0004t0016g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0003c0004t0026g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0003c0004t0080g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0003c0004t0109g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0004c0006t0029g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0004c0006t0075g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0004c0006t0087g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0004c0006t0088g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0004c0010t0010g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0005c0009t0013g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0006c0008t0008g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| a0007c0007t0026g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0046 | g0010 | EUR | GBR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0007 | EUR | GBR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00140 | hp1 | a0002 | c0002 | t0009 | g0337 | EUR | GBR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00140 | hp2 | a0001 | c0001 | t0012 | g0083 | EUR | GBR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00280 | hp2 | a0002 | c0002 | t0009 | g0024 | EUR | FIN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00323 | hp2 | a0001 | c0001 | t0131 | g0268 | EUR | FIN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00423 | hp1 | a0001 | c0001 | t0119 | g0283 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00423 | hp2 | a0002 | c0002 | t0009 | g0280 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00438 | hp1 | a0001 | c0001 | t0044 | g0229 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00438 | hp2 | a0001 | c0001 | t0140 | g0110 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00544 | hp2 | a0001 | c0001 | t0008 | g0282 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00558 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00558 | hp2 | a0002 | c0002 | t0004 | g0297 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00609 | hp1 | a0001 | c0001 | t0013 | g0132 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00609 | hp2 | a0002 | c0002 | t0004 | g0020 | EAS | CHS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00639 | hp1 | a0001 | c0001 | t0012 | g0003 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0151 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00642 | hp1 | a0001 | c0001 | t0015 | g0048 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00642 | hp2 | a0002 | c0002 | t0028 | g0327 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00733 | hp1 | a0001 | c0001 | t0020 | g0348 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00735 | hp1 | a0001 | c0001 | t0142 | g0156 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00738 | hp1 | a0001 | c0001 | t0083 | g0263 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00741 | hp1 | a0001 | c0001 | t0052 | g0347 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG00741 | hp2 | a0001 | c0001 | t0011 | g0081 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01069 | hp1 | a0001 | c0001 | t0136 | g0272 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0016 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01070 | hp2 | a0002 | c0002 | t0005 | g0338 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01071 | hp1 | a0002 | c0002 | t0005 | g0324 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0016 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0062 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01074 | hp2 | a0001 | c0001 | t0015 | g0006 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01081 | hp1 | a0001 | c0001 | t0015 | g0043 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01081 | hp2 | a0001 | c0001 | t0112 | g0040 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01099 | hp1 | a0002 | c0002 | t0005 | g0339 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01106 | hp2 | a0002 | c0002 | t0009 | g0024 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0028 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01109 | hp2 | a0001 | c0003 | t0007 | g0195 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01167 | hp1 | a0002 | c0002 | t0021 | g0025 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01167 | hp2 | a0001 | c0001 | t0015 | g0006 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01168 | hp1 | a0001 | c0001 | t0012 | g0111 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01175 | hp1 | a0001 | c0001 | t0046 | g0086 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01175 | hp2 | a0002 | c0002 | t0072 | g0336 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01192 | hp1 | a0001 | c0001 | t0011 | g0027 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01192 | hp2 | a0001 | c0001 | t0015 | g0044 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0059 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01243 | hp2 | a0001 | c0001 | t0048 | g0260 | AMR | PUR | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01256 | hp1 | a0002 | c0002 | t0005 | g0340 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01256 | hp2 | a0002 | c0002 | t0051 | g0023 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01257 | hp1 | a0001 | c0001 | t0090 | g0116 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01257 | hp2 | a0001 | c0001 | t0102 | g0142 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01258 | hp1 | a0002 | c0002 | t0005 | g0023 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01258 | hp2 | a0001 | c0001 | t0106 | g0143 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01261 | hp1 | a0001 | c0001 | t0008 | g0198 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01261 | hp2 | a0001 | c0001 | t0034 | g0105 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01346 | hp1 | a0001 | c0001 | t0128 | g0060 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01346 | hp2 | a0002 | c0002 | t0021 | g0025 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01358 | hp1 | a0001 | c0005 | t0100 | g0181 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01358 | hp2 | a0001 | c0001 | t0041 | g0026 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01361 | hp1 | a0001 | c0001 | t0127 | g0067 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01361 | hp2 | a0002 | c0002 | t0073 | g0345 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01433 | hp1 | a0001 | c0001 | t0011 | g0009 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01433 | hp2 | a0001 | c0001 | t0013 | g0095 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01496 | hp1 | a0001 | c0001 | t0011 | g0078 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0148 | EUR | IBS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01516 | hp2 | a0001 | c0001 | t0019 | g0240 | EUR | IBS | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01884 | hp1 | a0001 | c0001 | t0026 | g0259 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01884 | hp2 | a0001 | c0005 | t0007 | g0176 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01891 | hp1 | a0001 | c0001 | t0044 | g0055 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01891 | hp2 | a0001 | c0001 | t0032 | g0042 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01928 | hp1 | a0001 | c0001 | t0008 | g0187 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01928 | hp2 | a0001 | c0001 | t0027 | g0200 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01934 | hp1 | a0001 | c0001 | t0008 | g0188 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0054 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01943 | hp1 | a0001 | c0001 | t0010 | g0149 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01943 | hp2 | a0001 | c0001 | t0011 | g0080 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01975 | hp1 | a0001 | c0001 | t0129 | g0137 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0184 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01978 | hp1 | a0001 | c0001 | t0013 | g0087 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01978 | hp2 | a0001 | c0001 | t0126 | g0079 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01981 | hp1 | a0001 | c0001 | t0015 | g0047 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01981 | hp2 | a0001 | c0001 | t0035 | g0120 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01993 | hp1 | a0002 | c0002 | t0059 | g0332 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02004 | hp1 | a0001 | c0001 | t0035 | g0117 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02015 | hp1 | a0002 | c0002 | t0004 | g0300 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02015 | hp2 | a0002 | c0002 | t0064 | g0350 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02040 | hp1 | a0001 | c0001 | t0040 | g0069 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02040 | hp2 | a0001 | c0001 | t0006 | g0097 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02055 | hp1 | a0001 | c0001 | t0032 | g0041 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02055 | hp2 | a0003 | c0004 | t0016 | g0147 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02056 | hp2 | a0002 | c0002 | t0005 | g0001 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02071 | hp1 | a0001 | c0001 | t0038 | g0045 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02074 | hp1 | a0001 | c0001 | t0025 | g0096 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02074 | hp2 | a0002 | c0002 | t0023 | g0299 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02080 | hp1 | a0001 | c0001 | t0125 | g0075 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0109 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02083 | hp1 | a0001 | c0001 | t0093 | g0093 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02083 | hp2 | a0002 | c0002 | t0063 | g0294 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02129 | hp1 | a0002 | c0002 | t0004 | g0289 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02129 | hp2 | a0001 | c0001 | t0013 | g0107 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02132 | hp1 | a0002 | c0002 | t0004 | g0020 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02132 | hp2 | a0001 | c0001 | t0006 | g0057 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02145 | hp1 | a0001 | c0001 | t0120 | g0171 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02145 | hp2 | a0001 | c0001 | t0033 | g0264 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02148 | hp1 | a0001 | c0001 | t0008 | g0194 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02148 | hp2 | a0001 | c0001 | t0034 | g0098 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02155 | hp1 | a0002 | c0002 | t0065 | g0342 | EAS | CDX | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02155 | hp2 | a0002 | c0002 | t0022 | g0296 | EAS | CDX | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | CDX | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CDX | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02257 | hp1 | a0002 | c0002 | t0009 | g0329 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02257 | hp2 | a0001 | c0001 | t0107 | g0185 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02258 | hp1 | a0001 | c0005 | t0007 | g0173 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02258 | hp2 | a0001 | c0001 | t0039 | g0177 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02280 | hp2 | a0002 | c0002 | t0005 | g0320 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02293 | hp1 | a0001 | c0001 | t0011 | g0009 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02293 | hp2 | a0005 | c0009 | t0013 | g0125 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02451 | hp2 | a0001 | c0001 | t0039 | g0183 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02523 | hp2 | a0006 | c0008 | t0008 | g0284 | EAS | KHV | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02572 | hp1 | a0001 | c0001 | t0143 | g0230 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02572 | hp2 | a0001 | c0001 | t0017 | g0277 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02602 | hp1 | a0001 | c0001 | t0139 | g0219 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02602 | hp2 | a0002 | c0012 | t0057 | g0341 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02615 | hp1 | a0002 | c0002 | t0014 | g0022 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02615 | hp2 | a0001 | c0003 | t0045 | g0197 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02622 | hp2 | a0001 | c0001 | t0094 | g0050 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02630 | hp1 | a0001 | c0001 | t0017 | g0276 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02630 | hp2 | a0001 | c0003 | t0007 | g0189 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02647 | hp1 | a0001 | c0001 | t0104 | g0160 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02647 | hp2 | a0004 | c0006 | t0075 | g0255 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02717 | hp2 | a0001 | c0001 | t0033 | g0265 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02723 | hp1 | a0001 | c0001 | t0076 | g0065 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02723 | hp2 | a0002 | c0002 | t0014 | g0316 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02735 | hp1 | a0001 | c0001 | t0108 | g0152 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02735 | hp2 | a0001 | c0001 | t0115 | g0063 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02809 | hp1 | a0001 | c0001 | t0024 | g0008 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02809 | hp2 | a0001 | c0001 | t0017 | g0274 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02818 | hp1 | a0001 | c0001 | t0017 | g0279 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02818 | hp2 | a0001 | c0001 | t0141 | g0241 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02886 | hp1 | a0003 | c0004 | t0026 | g0165 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02886 | hp2 | a0001 | c0003 | t0099 | g0192 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02895 | hp1 | a0001 | c0001 | t0078 | g0275 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02896 | hp1 | a0001 | c0001 | t0122 | g0182 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02896 | hp2 | a0001 | c0001 | t0105 | g0159 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02922 | hp1 | a0001 | c0001 | t0024 | g0008 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02922 | hp2 | a0001 | c0005 | t0007 | g0175 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02965 | hp1 | a0001 | c0001 | t0096 | g0049 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02970 | hp1 | a0001 | c0001 | t0110 | g0161 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02970 | hp2 | a0001 | c0003 | t0007 | g0190 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02976 | hp1 | a0004 | c0006 | t0087 | g0167 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02976 | hp2 | a0003 | c0004 | t0016 | g0163 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03017 | hp2 | a0001 | c0001 | t0010 | g0162 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03041 | hp1 | a0001 | c0001 | t0082 | g0261 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03041 | hp2 | a0001 | c0005 | t0103 | g0174 | AFR | GWD | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03098 | hp1 | a0004 | c0006 | t0029 | g0019 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03098 | hp2 | a0001 | c0003 | t0045 | g0196 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03130 | hp1 | a0001 | c0005 | t0007 | g0179 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03130 | hp2 | a0003 | c0004 | t0080 | g0146 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03139 | hp1 | a0001 | c0003 | t0121 | g0178 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03139 | hp2 | a0002 | c0002 | t0014 | g0315 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03195 | hp1 | a0002 | c0002 | t0070 | g0323 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03195 | hp2 | a0001 | c0001 | t0079 | g0278 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03209 | hp1 | a0001 | c0003 | t0007 | g0015 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03225 | hp1 | a0002 | c0002 | t0014 | g0314 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03225 | hp2 | a0001 | c0001 | t0077 | g0051 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03239 | hp1 | a0002 | c0002 | t0054 | g0322 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03239 | hp2 | a0001 | c0001 | t0012 | g0012 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03453 | hp1 | a0001 | c0003 | t0007 | g0193 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03453 | hp2 | a0001 | c0001 | t0085 | g0254 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03486 | hp1 | a0002 | c0002 | t0062 | g0352 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03486 | hp2 | a0001 | c0003 | t0118 | g0180 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03491 | hp1 | a0002 | c0002 | t0058 | g0293 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03516 | hp1 | a0001 | c0001 | t0081 | g0258 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03579 | hp1 | a0001 | c0001 | t0117 | g0157 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03579 | hp2 | a0001 | c0001 | t0084 | g0249 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03654 | hp1 | a0001 | c0001 | t0010 | g0155 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03654 | hp2 | a0001 | c0001 | t0012 | g0141 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03669 | hp2 | a0002 | c0002 | t0005 | g0001 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03688 | hp1 | a0001 | c0001 | t0010 | g0154 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0061 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03704 | hp1 | a0001 | c0001 | t0132 | g0227 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03710 | hp1 | a0002 | c0002 | t0020 | g0298 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03831 | hp1 | a0001 | c0001 | t0124 | g0153 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03834 | hp1 | a0001 | c0001 | t0047 | g0203 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0030 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03927 | hp1 | a0002 | c0002 | t0060 | g0335 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0127 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03942 | hp1 | a0001 | c0001 | t0053 | g0318 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03942 | hp2 | a0002 | c0002 | t0020 | g0295 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG04115 | hp1 | a0001 | c0001 | t0092 | g0248 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG04115 | hp2 | a0002 | c0002 | t0005 | g0326 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG04184 | hp1 | a0002 | c0002 | t0028 | g0321 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG04184 | hp2 | a0001 | c0001 | t0018 | g0140 | SAS | BEB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG04199 | hp1 | a0001 | c0001 | t0042 | g0014 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG04199 | hp2 | a0001 | c0001 | t0042 | g0014 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG04204 | hp1 | a0002 | c0002 | t0021 | g0349 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG04204 | hp2 | a0001 | c0001 | t0010 | g0150 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG04228 | hp1 | a0001 | c0001 | t0012 | g0003 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG04228 | hp2 | a0002 | c0002 | t0005 | g0001 | SAS | STU | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18612 | hp1 | a0002 | c0002 | t0005 | g0001 | EAS | CHB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18612 | hp2 | a0001 | c0001 | t0137 | g0092 | EAS | CHB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18906 | hp1 | a0003 | c0004 | t0016 | g0145 | AFR | YRI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | YRI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18939 | hp1 | a0002 | c0002 | t0004 | g0305 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18939 | hp2 | a0002 | c0002 | t0009 | g0331 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18941 | hp1 | a0001 | c0001 | t0019 | g0222 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18944 | hp1 | a0001 | c0001 | t0089 | g0244 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18944 | hp2 | a0001 | c0001 | t0098 | g0257 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18947 | hp1 | a0002 | c0002 | t0009 | g0328 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18947 | hp2 | a0001 | c0001 | t0138 | g0212 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18948 | hp2 | a0001 | c0001 | t0027 | g0231 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18954 | hp2 | a0001 | c0001 | t0043 | g0243 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18956 | hp2 | a0002 | c0002 | t0004 | g0286 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18962 | hp1 | a0002 | c0013 | t0004 | g0310 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18964 | hp1 | a0002 | c0002 | t0022 | g0302 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18966 | hp2 | a0001 | c0001 | t0008 | g0191 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18970 | hp1 | a0001 | c0001 | t0091 | g0002 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18970 | hp2 | a0002 | c0002 | t0004 | g0287 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18971 | hp1 | a0001 | c0001 | t0018 | g0131 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18974 | hp1 | a0002 | c0002 | t0023 | g0004 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18977 | hp1 | a0001 | c0001 | t0011 | g0266 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18981 | hp1 | a0002 | c0002 | t0004 | g0301 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18981 | hp2 | a0001 | c0001 | t0056 | g0285 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18982 | hp1 | a0001 | c0001 | t0013 | g0115 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18982 | hp2 | a0001 | c0001 | t0036 | g0250 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18983 | hp1 | a0002 | c0002 | t0004 | g0288 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18983 | hp2 | a0002 | c0002 | t0004 | g0343 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18985 | hp1 | a0001 | c0001 | t0025 | g0245 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18991 | hp1 | a0001 | c0001 | t0040 | g0119 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18991 | hp2 | a0002 | c0002 | t0066 | g0291 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18998 | hp1 | a0002 | c0002 | t0009 | g0325 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18998 | hp2 | a0002 | c0002 | t0030 | g0292 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18999 | hp2 | a0001 | c0001 | t0116 | g0011 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19004 | hp1 | a0001 | c0001 | t0019 | g0210 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19005 | hp1 | a0002 | c0002 | t0004 | g0290 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19010 | hp1 | a0002 | c0002 | t0031 | g0021 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19011 | hp1 | a0001 | c0001 | t0019 | g0239 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19011 | hp2 | a0002 | c0002 | t0005 | g0330 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19012 | hp1 | a0001 | c0001 | t0101 | g0186 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19012 | hp2 | a0001 | c0001 | t0038 | g0169 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19030 | hp1 | a0001 | c0001 | t0049 | g0281 | AFR | LWK | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19030 | hp2 | a0004 | c0006 | t0029 | g0019 | AFR | LWK | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19043 | hp1 | a0001 | c0001 | t0061 | g0056 | AFR | LWK | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19055 | hp1 | a0002 | c0002 | t0004 | g0311 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19055 | hp2 | a0001 | c0001 | t0111 | g0010 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19056 | hp2 | a0002 | c0002 | t0022 | g0304 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19057 | hp1 | a0002 | c0002 | t0004 | g0303 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19057 | hp2 | a0002 | c0002 | t0030 | g0306 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19058 | hp1 | a0001 | c0001 | t0097 | g0256 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19058 | hp2 | a0001 | c0001 | t0027 | g0207 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19060 | hp1 | a0002 | c0002 | t0067 | g0309 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19063 | hp1 | a0001 | c0001 | t0025 | g0133 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19063 | hp2 | a0002 | c0002 | t0069 | g0313 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19064 | hp1 | a0002 | c0002 | t0031 | g0021 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19064 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19067 | hp1 | a0002 | c0002 | t0130 | g0168 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19070 | hp1 | a0001 | c0001 | t0113 | g0012 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19074 | hp1 | a0001 | c0001 | t0047 | g0232 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19074 | hp2 | a0001 | c0001 | t0036 | g0013 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19079 | hp1 | a0002 | c0002 | t0023 | g0312 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19079 | hp2 | a0001 | c0001 | t0134 | g0209 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19080 | hp1 | a0002 | c0002 | t0005 | g0001 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19081 | hp1 | a0001 | c0001 | t0135 | g0211 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19081 | hp2 | a0001 | c0001 | t0037 | g0089 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19082 | hp1 | a0001 | c0001 | t0043 | g0121 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19083 | hp1 | a0002 | c0002 | t0050 | g0307 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19084 | hp1 | a0002 | c0002 | t0071 | g0333 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19087 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19088 | hp1 | a0002 | c0002 | t0018 | g0170 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19088 | hp2 | a0001 | c0001 | t0114 | g0071 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19089 | hp1 | a0001 | c0001 | t0037 | g0135 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19089 | hp2 | a0001 | c0001 | t0013 | g0073 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19091 | hp1 | a0001 | c0001 | t0018 | g0085 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19240 | hp1 | a0001 | c0001 | t0123 | g0005 | AFR | YRI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA19240 | hp2 | a0001 | c0001 | t0055 | g0308 | AFR | YRI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA20129 | hp2 | a0001 | c0001 | t0041 | g0158 | AFR | ASW | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA20752 | hp1 | a0002 | c0002 | t0005 | g0319 | EUR | TSI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA20752 | hp2 | a0004 | c0010 | t0010 | g0246 | EUR | TSI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA20805 | hp1 | a0001 | c0001 | t0133 | g0221 | EUR | TSI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA20805 | hp2 | a0001 | c0001 | t0012 | g0066 | EUR | TSI | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | GIH | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | GIH | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01123 | hp1 | a0002 | c0002 | t0005 | g0344 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG01123 | hp2 | a0002 | c0002 | t0009 | g0334 | AMR | CLM | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02109 | hp1 | a0003 | c0004 | t0016 | g0144 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02109 | hp2 | a0002 | c0002 | t0014 | g0317 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02486 | hp1 | a0001 | c0001 | t0086 | g0262 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02559 | hp1 | a0004 | c0006 | t0088 | g0166 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG02559 | hp2 | a0001 | c0001 | t0024 | g0064 | AFR | ACB | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03471 | hp1 | a0001 | c0003 | t0007 | g0015 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG03471 | hp2 | a0007 | c0007 | t0026 | g0029 | AFR | MSL | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG06807 | hp1 | a0003 | c0004 | t0109 | g0199 | AFR | USA | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| HG06807 | hp2 | a0001 | c0011 | t0068 | g0351 | AFR | USA | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA20300 | hp1 | a0003 | c0004 | t0016 | g0164 | AFR | USA | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | USA | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA21309 | hp1 | a0002 | c0002 | t0014 | g0022 | AFR | LWK | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| NA21309 | hp2 | a0001 | c0001 | t0095 | g0046 | AFR | LWK | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0074 | g0346 | REF | REF | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0012 | g0003 | REF | REF | LIPG_chr18_49557057_49604185 | LIPG | chr18 | 49557057 | 49604185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:49562384 | G | A | 1 | a0003 | 8 | HG02055.hp2 HG02109.hp1 HG02886.hp1 others(5): Show |
missense_variant | MODERATE | c.76G>A | p.Gly26Ser | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/10 | 328/10418 | 76/1503 | 26/500 | chr18 | 49562384 | |||
| chr18:49567494 | C | T | 1 | a0002 | 84 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(81): Show |
missense_variant | MODERATE | c.332C>T | p.Thr111Ile | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/10 | 584/10418 | 332/1503 | 111/500 | chr18 | 49567494 | |||
| chr18:49581514 | C | G | 1 | a0004 | 5 | HG02559.hp1 HG02647.hp2 HG02976.hp1 others(2): Show |
missense_variant | MODERATE | c.893C>G | p.Thr298Ser | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/10 | 1145/10418 | 893/1503 | 298/500 | chr18 | 49581514 | |||
| chr18:49581514 | C | T | 1 | a0004 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.893C>T | p.Thr298Ile | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/10 | 1145/10418 | 893/1503 | 298/500 | chr18 | 49581514 | |||
| chr18:49581535 | A | G | 1 | a0005 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.914A>G | p.Lys305Arg | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/10 | 1166/10418 | 914/1503 | 305/500 | chr18 | 49581535 | |||
| chr18:49582407 | T | C | 1 | a0007 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1082T>C | p.Met361Thr | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/10 | 1334/10418 | 1082/1503 | 361/500 | chr18 | 49582407 | |||
| chr18:49583689 | C | T | 1 | a0006 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1291C>T | p.Arg431Cys | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/10 | 1543/10418 | 1291/1503 | 431/500 | chr18 | 49583689 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:49562320 | C | A | 1 | a0001c0003 | 11 | HG01109.hp2 HG02615.hp2 HG02630.hp2 others(8): Show |
synonymous_variant | LOW | c.12C>A | p.Ser4Ser | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/10 | 264/10418 | 12/1503 | 4/500 | chr18 | 49562320 | |||
| chr18:49562371 | C | T | 2 | a0001c0003 a0001c0005 |
17 | HG01109.hp2 HG01358.hp1 HG01884.hp2 others(14): Show |
synonymous_variant | LOW | c.63C>T | p.Ser21Ser | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/10 | 315/10418 | 63/1503 | 21/500 | chr18 | 49562371 | |||
| chr18:49569487 | C | T | 1 | a0001c0011 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.510C>T | p.Leu170Leu | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/10 | 762/10418 | 510/1503 | 170/500 | chr18 | 49569487 | |||
| chr18:49575382 | C | G | 1 | a0002c0013 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.585C>G | p.Ala195Ala | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/10 | 837/10418 | 585/1503 | 195/500 | chr18 | 49575382 | |||
| chr18:49581629 | A | T | 1 | a0002c0012 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.1008A>T | p.Leu336Leu | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/10 | 1260/10418 | 1008/1503 | 336/500 | chr18 | 49581629 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:49562092 | A | G | 1 | a0001c0001t0143 | 1 | HG02572.hp1 | 5_prime_UTR_variant | MODIFIER | c.-217A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/10 | 217 | chr18 | 49562092 | ||||||
| chr18:49562285 | T | G | 41 | a0001c0001t0020 a0001c0001t0048 a0001c0001t0049 others(38): Show |
94 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(91): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-24T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/10 | chr18 | 49562285 | |||||||
| chr18:49590746 | C | T | 1 | a0004c0006t0075 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*224C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 224 | chr18 | 49590746 | ||||||
| chr18:49590764 | G | C | 1 | a0001c0001t0032 | 2 | HG01891.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*242G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 242 | chr18 | 49590764 | ||||||
| chr18:49590804 | T | C | 38 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0024 others(35): Show |
83 | HG00544.hp1 HG00738.hp1 HG00738.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*282T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 282 | chr18 | 49590804 | ||||||
| chr18:49590837 | A | G | 6 | a0001c0001t0142 a0002c0002t0009 a0002c0002t0070 others(3): Show |
14 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*315A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 315 | chr18 | 49590837 | ||||||
| chr18:49590868 | G | A | 2 | a0001c0001t0039 a0004c0006t0075 |
3 | HG02258.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*346G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 346 | chr18 | 49590868 | ||||||
| chr18:49590883 | C | T | 2 | a0001c0001t0097 a0001c0001t0098 |
2 | NA18944.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*361C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 361 | chr18 | 49590883 | ||||||
| chr18:49590951 | G | A | 2 | a0001c0001t0076 a0001c0001t0077 |
2 | HG02723.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*429G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 429 | chr18 | 49590951 | ||||||
| chr18:49590970 | C | T | 7 | a0001c0001t0038 a0001c0001t0039 a0001c0001t0094 others(4): Show |
9 | HG02071.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*448C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 448 | chr18 | 49590970 | ||||||
| chr18:49591001 | C | T | 4 | a0001c0001t0038 a0001c0001t0094 a0001c0001t0095 others(1): Show |
5 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*479C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 479 | chr18 | 49591001 | ||||||
| chr18:49591004 | A | G | 73 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0015 others(70): Show |
189 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*482A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 482 | chr18 | 49591004 | ||||||
| chr18:49591006 | C | T | 12 | a0001c0001t0002 a0001c0001t0034 a0001c0001t0035 others(9): Show |
45 | HG00438.hp2 HG00544.hp1 HG00738.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*484C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 484 | chr18 | 49591006 | ||||||
| chr18:49591078 | A | G | 11 | a0001c0001t0038 a0001c0001t0039 a0001c0001t0094 others(8): Show |
13 | HG02071.hp1 HG02258.hp2 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*556A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 556 | chr18 | 49591078 | ||||||
| chr18:49591407 | C | T | 2 | a0001c0001t0039 a0004c0006t0075 |
3 | HG02258.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*885C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 885 | chr18 | 49591407 | ||||||
| chr18:49591430 | G | A | 2 | a0001c0001t0039 a0004c0006t0075 |
3 | HG02258.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*908G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 908 | chr18 | 49591430 | ||||||
| chr18:49591539 | A | G | 2 | a0001c0001t0097 a0001c0001t0098 |
2 | NA18944.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1017A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1017 | chr18 | 49591539 | ||||||
| chr18:49591543 | C | CATACAGA others(7): Show |
1 | a0001c0001t0141 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1022_*1023insTACA others(10): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1023 | INFO_REALIGN_3_PRIME | chr18 | 49591543 | |||||
| chr18:49591564 | C | T | 2 | a0001c0001t0039 a0004c0006t0075 |
3 | HG02258.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1042C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1042 | chr18 | 49591564 | ||||||
| chr18:49591582 | G | A | 1 | a0001c0001t0032 | 2 | HG01891.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1060G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1060 | chr18 | 49591582 | ||||||
| chr18:49591609 | T | A | 12 | a0001c0001t0002 a0001c0001t0034 a0001c0001t0035 others(9): Show |
45 | HG00438.hp2 HG00544.hp1 HG00738.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1087T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1087 | chr18 | 49591609 | ||||||
| chr18:49591729 | C | T | 2 | a0001c0001t0039 a0004c0006t0075 |
3 | HG02258.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1207C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1207 | chr18 | 49591729 | ||||||
| chr18:49591800 | A | G | 13 | a0001c0001t0024 a0001c0001t0032 a0001c0001t0033 others(10): Show |
17 | HG00738.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1278A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1278 | chr18 | 49591800 | ||||||
| chr18:49591805 | A | C | 1 | a0002c0002t0069 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1283A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1283 | chr18 | 49591805 | ||||||
| chr18:49591806 | C | A | 1 | a0002c0002t0069 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1284C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1284 | chr18 | 49591806 | ||||||
| chr18:49591849 | T | C | 12 | a0001c0001t0002 a0001c0001t0034 a0001c0001t0035 others(9): Show |
45 | HG00438.hp2 HG00544.hp1 HG00738.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1327T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1327 | chr18 | 49591849 | ||||||
| chr18:49591931 | T | C | 1 | a0001c0003t0099 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1409T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1409 | chr18 | 49591931 | ||||||
| chr18:49591948 | A | G | 1 | a0001c0001t0129 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1426A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1426 | chr18 | 49591948 | ||||||
| chr18:49591978 | CT | C | 4 | a0001c0001t0034 a0001c0001t0035 a0001c0001t0090 others(1): Show |
6 | HG01257.hp1 HG01261.hp2 HG01358.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1466delT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1466 | INFO_REALIGN_3_PRIME | chr18 | 49591978 | |||||
| chr18:49591988 | T | A | 1 | a0001c0001t0089 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1466T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1466 | chr18 | 49591988 | ||||||
| chr18:49592028 | T | C | 36 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0018 others(33): Show |
98 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1506T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1506 | chr18 | 49592028 | ||||||
| chr18:49592226 | A | G | 1 | a0001c0001t0061 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1704A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1704 | chr18 | 49592226 | ||||||
| chr18:49592229 | A | G | 1 | a0001c0001t0086 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1707A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1707 | chr18 | 49592229 | ||||||
| chr18:49592236 | C | T | 1 | a0002c0002t0069 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1714C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1714 | chr18 | 49592236 | ||||||
| chr18:49592237 | T | C | 1 | a0002c0002t0069 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1715T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1715 | chr18 | 49592237 | ||||||
| chr18:49592388 | A | G | 4 | a0001c0001t0039 a0001c0001t0097 a0001c0001t0098 others(1): Show |
5 | HG02258.hp2 HG02451.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1866A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1866 | chr18 | 49592388 | ||||||
| chr18:49592485 | C | T | 1 | a0001c0001t0128 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1963C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1963 | chr18 | 49592485 | ||||||
| chr18:49592521 | T | C | 1 | a0001c0001t0101 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1999T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 1999 | chr18 | 49592521 | ||||||
| chr18:49592525 | G | A | 1 | a0002c0002t0062 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2003G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2003 | chr18 | 49592525 | ||||||
| chr18:49592553 | T | G | 55 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0018 others(52): Show |
123 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2031T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2031 | chr18 | 49592553 | ||||||
| chr18:49592575 | A | AGTTTTGG others(10): Show |
1 | a0001c0001t0139 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2054_*2070dupGTTT others(13): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2071 | INFO_REALIGN_3_PRIME | chr18 | 49592575 | |||||
| chr18:49592816 | TA | T | 9 | a0001c0001t0038 a0001c0001t0039 a0001c0001t0094 others(6): Show |
11 | HG02071.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2301delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2301 | INFO_REALIGN_3_PRIME | chr18 | 49592816 | |||||
| chr18:49592919 | A | G | 1 | a0001c0001t0032 | 2 | HG01891.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2397A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2397 | chr18 | 49592919 | ||||||
| chr18:49592924 | A | AT | 35 | a0001c0001t0002 a0001c0001t0019 a0001c0001t0025 others(32): Show |
81 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2428dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | |||||
| chr18:49592924 | A | ATT | 18 | a0001c0001t0018 a0001c0001t0035 a0001c0001t0081 others(15): Show |
39 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2427_*2428dupTT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | |||||
| chr18:49592924 | A | ATTT | 4 | a0001c0001t0048 a0002c0002t0023 a0002c0002t0066 others(1): Show |
6 | HG01243.hp2 HG02074.hp2 NA18974.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2426_*2428dupTTT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | |||||
| chr18:49592924 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0098 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2419_*2428dupTTTT others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | |||||
| chr18:49592924 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0038 a0001c0001t0094 |
3 | HG02071.hp1 HG02622.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2418_*2428dupTTTT others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | |||||
| chr18:49592924 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0095 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2417_*2428dupTTTT others(8): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | |||||
| chr18:49592924 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0096 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2416_*2428dupTTTT others(9): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | |||||
| chr18:49592924 | AT | A | 14 | a0001c0001t0017 a0001c0001t0024 a0001c0001t0027 others(11): Show |
23 | HG00323.hp2 HG00738.hp1 HG01256.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2428delT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2428 | INFO_REALIGN_3_PRIME | chr18 | 49592924 | |||||
| chr18:49592974 | C | T | 17 | a0001c0001t0001 a0001c0001t0015 a0001c0001t0019 others(14): Show |
65 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2452C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2452 | chr18 | 49592974 | ||||||
| chr18:49593004 | C | T | 1 | a0001c0011t0068 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2482C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2482 | chr18 | 49593004 | ||||||
| chr18:49593053 | T | C | 147 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(144): Show |
371 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(368): Show |
3_prime_UTR_variant | MODIFIER | c.*2531T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2531 | chr18 | 49593053 | ||||||
| chr18:49593058 | G | A | 1 | a0001c0001t0039 | 2 | HG02258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2536G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2536 | chr18 | 49593058 | ||||||
| chr18:49593159 | C | T | 10 | a0001c0001t0024 a0001c0001t0032 a0001c0001t0033 others(7): Show |
14 | HG00738.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2637C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2637 | chr18 | 49593159 | ||||||
| chr18:49593176 | G | A | 1 | a0001c0001t0123 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2654G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2654 | chr18 | 49593176 | ||||||
| chr18:49593209 | A | G | 55 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0018 others(52): Show |
123 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2687A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2687 | chr18 | 49593209 | ||||||
| chr18:49593241 | A | G | 2 | a0001c0001t0084 a0001c0001t0085 |
2 | HG03453.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2719A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2719 | chr18 | 49593241 | ||||||
| chr18:49593283 | C | G | 1 | a0002c0002t0058 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2761C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2761 | chr18 | 49593283 | ||||||
| chr18:49593285 | G | A | 1 | a0001c0001t0085 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2763G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2763 | chr18 | 49593285 | ||||||
| chr18:49593344 | G | T | 3 | a0001c0001t0132 a0002c0002t0060 a0002c0012t0057 |
3 | HG02602.hp2 HG03704.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2822G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2822 | chr18 | 49593344 | ||||||
| chr18:49593373 | C | A | 2 | a0004c0006t0087 a0004c0006t0088 |
2 | HG02559.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2851C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 2851 | chr18 | 49593373 | ||||||
| chr18:49593570 | A | C | 1 | a0001c0001t0039 | 2 | HG02258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3048A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3048 | chr18 | 49593570 | ||||||
| chr18:49593585 | G | C | 1 | a0001c0001t0090 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3063G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3063 | chr18 | 49593585 | ||||||
| chr18:49593690 | G | A | 1 | a0001c0001t0096 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3168G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3168 | chr18 | 49593690 | ||||||
| chr18:49593738 | G | C | 1 | a0002c0002t0072 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3216G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3216 | chr18 | 49593738 | ||||||
| chr18:49593787 | G | A | 1 | a0001c0001t0138 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3265G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3265 | chr18 | 49593787 | ||||||
| chr18:49593820 | T | C | 8 | a0001c0001t0033 a0001c0001t0048 a0001c0001t0081 others(5): Show |
9 | HG00738.hp1 HG01243.hp2 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3298T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3298 | chr18 | 49593820 | ||||||
| chr18:49593838 | C | T | 1 | a0001c0001t0056 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3316C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3316 | chr18 | 49593838 | ||||||
| chr18:49593936 | G | C | 2 | a0001c0001t0104 a0001c0001t0105 |
2 | HG02647.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3414G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3414 | chr18 | 49593936 | ||||||
| chr18:49594121 | G | A | 1 | a0001c0001t0124 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3599G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3599 | chr18 | 49594121 | ||||||
| chr18:49594129 | T | G | 27 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0034 others(24): Show |
64 | HG00438.hp2 HG00544.hp1 HG00738.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3607T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3607 | chr18 | 49594129 | ||||||
| chr18:49594143 | G | GT | 17 | a0001c0001t0001 a0001c0001t0015 a0001c0001t0019 others(14): Show |
65 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*3630dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3631 | INFO_REALIGN_3_PRIME | chr18 | 49594143 | |||||
| chr18:49594193 | G | C | 6 | a0001c0001t0024 a0001c0001t0032 a0001c0001t0049 others(3): Show |
9 | HG01891.hp2 HG02055.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3671G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3671 | chr18 | 49594193 | ||||||
| chr18:49594198 | G | C | 1 | a0002c0002t0058 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3676G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3676 | chr18 | 49594198 | ||||||
| chr18:49594230 | G | A | 49 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0018 others(46): Show |
115 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*3708G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3708 | chr18 | 49594230 | ||||||
| chr18:49594403 | G | A | 1 | a0001c0001t0091 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3881G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3881 | chr18 | 49594403 | ||||||
| chr18:49594425 | G | A | 2 | a0001c0001t0102 a0001c0001t0106 |
2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3903G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3903 | chr18 | 49594425 | ||||||
| chr18:49594441 | T | A | 1 | a0001c0001t0107 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3919T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3919 | chr18 | 49594441 | ||||||
| chr18:49594454 | C | T | 1 | a0001c0001t0084 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3932C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3932 | chr18 | 49594454 | ||||||
| chr18:49594490 | T | A | 3 | a0001c0001t0033 a0001c0001t0083 a0001c0001t0086 |
4 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3968T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3968 | chr18 | 49594490 | ||||||
| chr18:49594520 | G | A | 1 | a0001c0001t0039 | 2 | HG02258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3998G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 3998 | chr18 | 49594520 | ||||||
| chr18:49594533 | C | T | 3 | a0001c0001t0033 a0001c0001t0083 a0001c0001t0086 |
4 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4011C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4011 | chr18 | 49594533 | ||||||
| chr18:49594616 | A | T | 18 | a0001c0001t0001 a0001c0001t0015 a0001c0001t0019 others(15): Show |
67 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*4094A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4094 | chr18 | 49594616 | ||||||
| chr18:49594623 | G | A | 6 | a0001c0001t0024 a0001c0001t0032 a0001c0001t0049 others(3): Show |
9 | HG01891.hp2 HG02055.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4101G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4101 | chr18 | 49594623 | ||||||
| chr18:49594747 | T | C | 5 | a0001c0001t0010 a0001c0001t0042 a0001c0001t0061 others(2): Show |
12 | HG00639.hp2 HG01516.hp1 HG01943.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4225T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4225 | chr18 | 49594747 | ||||||
| chr18:49594946 | G | T | 44 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0015 others(41): Show |
129 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*4424G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4424 | chr18 | 49594946 | ||||||
| chr18:49595201 | G | C | 5 | a0001c0001t0017 a0001c0001t0078 a0001c0001t0079 others(2): Show |
12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4679G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4679 | chr18 | 49595201 | ||||||
| chr18:49595267 | A | C | 2 | a0001c0001t0104 a0001c0001t0105 |
2 | HG02647.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4745A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4745 | chr18 | 49595267 | ||||||
| chr18:49595306 | G | A | 1 | a0003c0004t0109 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4784G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4784 | chr18 | 49595306 | ||||||
| chr18:49595328 | A | G | 40 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0015 others(37): Show |
112 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*4806A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4806 | chr18 | 49595328 | ||||||
| chr18:49595329 | G | T | 1 | a0001c0001t0137 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4807G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4807 | chr18 | 49595329 | ||||||
| chr18:49595412 | T | C | 3 | a0001c0001t0104 a0001c0001t0105 a0001c0001t0110 |
3 | HG02647.hp1 HG02896.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4890T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 4890 | chr18 | 49595412 | ||||||
| chr18:49595606 | G | A | 1 | a0001c0001t0039 | 2 | HG02258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5084G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5084 | chr18 | 49595606 | ||||||
| chr18:49595625 | C | T | 1 | a0001c0001t0096 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5103C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5103 | chr18 | 49595625 | ||||||
| chr18:49595689 | G | A | 1 | a0001c0001t0077 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5167G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5167 | chr18 | 49595689 | ||||||
| chr18:49595721 | C | T | 3 | a0001c0001t0048 a0001c0001t0081 a0001c0001t0082 |
3 | HG01243.hp2 HG03041.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5199C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5199 | chr18 | 49595721 | ||||||
| chr18:49595783 | A | G | 2 | a0001c0001t0084 a0001c0001t0085 |
2 | HG03453.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5261A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5261 | chr18 | 49595783 | ||||||
| chr18:49595788 | A | C | 26 | a0001c0001t0002 a0001c0001t0024 a0001c0001t0032 others(23): Show |
62 | HG00438.hp2 HG00544.hp1 HG00738.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*5266A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5266 | chr18 | 49595788 | ||||||
| chr18:49595904 | GGCCTATT others(44): Show |
G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5383_*5433delGCCT others(47): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5383 | chr18 | 49595904 | ||||||
| chr18:49596272 | C | T | 2 | a0001c0001t0097 a0001c0001t0098 |
2 | NA18944.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5750C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5750 | chr18 | 49596272 | ||||||
| chr18:49596362 | G | A | 4 | a0001c0001t0013 a0001c0001t0043 a0001c0001t0111 others(1): Show |
10 | HG00609.hp1 HG01433.hp2 HG01978.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5840G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5840 | chr18 | 49596362 | ||||||
| chr18:49596484 | A | G | 25 | a0001c0001t0011 a0001c0001t0038 a0001c0001t0041 others(22): Show |
59 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*5962A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 5962 | chr18 | 49596484 | ||||||
| chr18:49596551 | C | A | 36 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0026 others(33): Show |
93 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*6029C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6029 | chr18 | 49596551 | ||||||
| chr18:49596573 | T | G | 6 | a0001c0001t0010 a0001c0001t0042 a0001c0001t0061 others(3): Show |
13 | HG00639.hp2 HG01257.hp2 HG01258.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6051T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6051 | chr18 | 49596573 | ||||||
| chr18:49596610 | G | T | 1 | a0002c0002t0069 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6088G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6088 | chr18 | 49596610 | ||||||
| chr18:49596635 | C | CA | 46 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0026 others(43): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*6136dupA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6137 | INFO_REALIGN_3_PRIME | chr18 | 49596635 | |||||
| chr18:49596635 | C | CAA | 10 | a0001c0001t0041 a0001c0001t0049 a0001c0001t0086 others(7): Show |
12 | HG00423.hp1 HG00642.hp2 HG01358.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6135_*6136dupAA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6137 | INFO_REALIGN_3_PRIME | chr18 | 49596635 | |||||
| chr18:49596635 | CA | C | 8 | a0001c0001t0047 a0001c0001t0078 a0001c0001t0105 others(5): Show |
9 | HG02155.hp1 HG02735.hp1 HG02735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6136delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6136 | INFO_REALIGN_3_PRIME | chr18 | 49596635 | |||||
| chr18:49596635 | CAAAAAA | C | 2 | a0003c0004t0016 a0003c0004t0080 |
6 | HG02055.hp2 HG02109.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6131_*6136delAAAA others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6131 | INFO_REALIGN_3_PRIME | chr18 | 49596635 | |||||
| chr18:49596691 | A | G | 1 | a0001c0001t0136 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6169A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6169 | chr18 | 49596691 | ||||||
| chr18:49596752 | C | T | 28 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0026 others(25): Show |
76 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*6230C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6230 | chr18 | 49596752 | ||||||
| chr18:49596867 | T | C | 44 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(41): Show |
109 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*6345T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6345 | chr18 | 49596867 | ||||||
| chr18:49596928 | T | C | 2 | a0001c0001t0076 a0001c0001t0077 |
2 | HG02723.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6406T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6406 | chr18 | 49596928 | ||||||
| chr18:49597393 | C | T | 31 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0038 others(28): Show |
70 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*6871C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6871 | chr18 | 49597393 | ||||||
| chr18:49597411 | C | G | 1 | a0002c0002t0064 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6889C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6889 | chr18 | 49597411 | ||||||
| chr18:49597489 | A | AAAGTCAA others(4): Show |
1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6968_*6969insAGTC others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6969 | INFO_REALIGN_3_PRIME | chr18 | 49597489 | |||||
| chr18:49597492 | A | C | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6970A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6970 | chr18 | 49597492 | ||||||
| chr18:49597493 | T | A | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6971T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6971 | chr18 | 49597493 | ||||||
| chr18:49597496 | A | T | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6974A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6974 | chr18 | 49597496 | ||||||
| chr18:49597513 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6991T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6991 | chr18 | 49597513 | ||||||
| chr18:49597515 | G | GGAGGGCG others(20): Show |
1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6993_*6994insGAGG others(23): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6994 | chr18 | 49597515 | ||||||
| chr18:49597516 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6994T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6994 | chr18 | 49597516 | ||||||
| chr18:49597517 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6995T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6995 | chr18 | 49597517 | ||||||
| chr18:49597518 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6996T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 6996 | chr18 | 49597518 | ||||||
| chr18:49597522 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7000T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7000 | chr18 | 49597522 | ||||||
| chr18:49597530 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7008T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7008 | chr18 | 49597530 | ||||||
| chr18:49597535 | T | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7013T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7013 | chr18 | 49597535 | ||||||
| chr18:49597538 | T | C | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7016T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7016 | chr18 | 49597538 | ||||||
| chr18:49597539 | C | G | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7017C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7017 | chr18 | 49597539 | ||||||
| chr18:49597551 | A | T | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7029A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7029 | chr18 | 49597551 | ||||||
| chr18:49597552 | C | T | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7030C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7030 | chr18 | 49597552 | ||||||
| chr18:49597555 | T | A | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7033T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7033 | chr18 | 49597555 | ||||||
| chr18:49597556 | G | T | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7034G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7034 | chr18 | 49597556 | ||||||
| chr18:49597557 | A | T | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7035A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7035 | chr18 | 49597557 | ||||||
| chr18:49597562 | C | T | 1 | a0002c0002t0071 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7040C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7040 | chr18 | 49597562 | ||||||
| chr18:49597634 | G | T | 1 | a0001c0001t0112 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7112G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7112 | chr18 | 49597634 | ||||||
| chr18:49597668 | G | A | 12 | a0001c0001t0018 a0001c0001t0096 a0001c0001t0135 others(9): Show |
31 | HG00558.hp2 HG00609.hp2 HG02015.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*7146G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7146 | chr18 | 49597668 | ||||||
| chr18:49598211 | T | C | 4 | a0001c0001t0026 a0002c0002t0014 a0003c0004t0026 others(1): Show |
9 | HG01884.hp1 HG02109.hp2 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7689T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7689 | chr18 | 49598211 | ||||||
| chr18:49598218 | A | G | 1 | a0001c0001t0083 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7696A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7696 | chr18 | 49598218 | ||||||
| chr18:49598255 | C | T | 1 | a0001c0001t0095 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7733C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7733 | chr18 | 49598255 | ||||||
| chr18:49598271 | T | G | 2 | a0001c0001t0131 a0002c0002t0021 |
4 | HG00323.hp2 HG01167.hp1 HG01346.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7749T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 7749 | chr18 | 49598271 | ||||||
| chr18:49598538 | C | T | 4 | a0001c0001t0094 a0001c0001t0104 a0001c0001t0105 others(1): Show |
4 | HG02622.hp2 HG02647.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8016C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 8016 | chr18 | 49598538 | ||||||
| chr18:49598612 | C | G | 15 | a0001c0001t0002 a0001c0001t0034 a0001c0001t0035 others(12): Show |
49 | HG00438.hp2 HG00544.hp1 HG00738.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*8090C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 8090 | chr18 | 49598612 | ||||||
| chr18:49598616 | T | G | 1 | a0001c0001t0119 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8094T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 8094 | chr18 | 49598616 | ||||||
| chr18:49599002 | G | A | 36 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0032 others(33): Show |
76 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*8480G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 8480 | chr18 | 49599002 | ||||||
| chr18:49599055 | T | C | 2 | a0001c0001t0102 a0001c0001t0106 |
2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8533T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 10/10 | 8533 | chr18 | 49599055 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:49562451 | G | A | 3 | a0001c0001t0011g0027 a0001c0001t0011g0028 a0001c0001t0041g0026 |
3 | HG01109.hp1 HG01192.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.97+46G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562451 | |||||||
| chr18:49562456 | C | T | 77 | a0001c0001t0020g0348 a0001c0001t0052g0347 a0001c0001t0053g0318 others(74): Show |
87 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.97+51C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562456 | |||||||
| chr18:49562460 | C | G | 77 | a0001c0001t0020g0348 a0001c0001t0052g0347 a0001c0001t0053g0318 others(74): Show |
87 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.97+55C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562460 | |||||||
| chr18:49562512 | C | T | 3 | a0001c0001t0008g0282 a0001c0001t0119g0283 a0006c0008t0008g0284 |
3 | HG00423.hp1 HG00544.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.97+107C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562512 | |||||||
| chr18:49562545 | C | G | 1 | a0001c0001t0049g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97+140C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562545 | |||||||
| chr18:49562705 | G | T | 1 | a0002c0002t0062g0352 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97+300G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562705 | |||||||
| chr18:49562707 | C | T | 45 | a0001c0001t0020g0348 a0001c0001t0052g0347 a0001c0001t0053g0318 others(42): Show |
52 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.97+302C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562707 | |||||||
| chr18:49562728 | T | C | 16 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(13): Show |
16 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+323T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562728 | |||||||
| chr18:49562823 | G | C | 1 | a0001c0001t0049g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97+418G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562823 | |||||||
| chr18:49562872 | G | A | 9 | a0001c0001t0015g0006 a0001c0001t0015g0043 a0001c0001t0015g0044 others(6): Show |
10 | HG00642.hp1 HG01074.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.97+467G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49562872 | |||||||
| chr18:49563316 | G | C | 5 | a0002c0002t0014g0022 a0002c0002t0014g0314 a0002c0002t0014g0315 others(2): Show |
6 | HG02109.hp2 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+911G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563316 | |||||||
| chr18:49563371 | C | T | 1 | a0001c0001t0049g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97+966C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563371 | |||||||
| chr18:49563430 | A | G | 1 | a0001c0011t0068g0351 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.97+1025A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563430 | |||||||
| chr18:49563442 | G | A | 1 | a0001c0001t0077g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97+1037G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563442 | |||||||
| chr18:49563458 | T | C | 1 | a0001c0001t0053g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.97+1053T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563458 | |||||||
| chr18:49563547 | AAGAC | A | 7 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.97+1149_97+1152del others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | 49563547 | ||||||
| chr18:49563601 | A | G | 5 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(2): Show |
5 | HG01069.hp1 HG01070.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+1196A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563601 | |||||||
| chr18:49563616 | G | A | 2 | a0001c0001t0002g0052 a0001c0001t0002g0053 |
2 | HG01099.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.97+1211G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563616 | |||||||
| chr18:49563623 | G | A | 1 | a0001c0001t0077g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97+1218G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563623 | |||||||
| chr18:49563691 | G | C | 1 | a0007c0007t0026g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.97+1286G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563691 | |||||||
| chr18:49563722 | A | G | 1 | a0001c0001t0049g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97+1317A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563722 | |||||||
| chr18:49563805 | T | C | 11 | a0001c0001t0003g0061 a0001c0001t0006g0007 a0001c0001t0006g0054 others(8): Show |
12 | HG00099.hp2 HG01074.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.97+1400T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563805 | |||||||
| chr18:49563889 | G | C | 7 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(4): Show |
7 | HG02572.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-1428G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563889 | |||||||
| chr18:49563921 | A | G | 2 | a0001c0001t0001g0267 a0001c0001t0131g0268 |
2 | HG00323.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.98-1396A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49563921 | |||||||
| chr18:49564031 | T | C | 1 | a0001c0001t0049g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.98-1286T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564031 | |||||||
| chr18:49564131 | C | T | 1 | a0001c0001t0015g0006 | 2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.98-1186C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564131 | |||||||
| chr18:49564361 | G | A | 1 | a0002c0002t0005g0319 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.98-956G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564361 | |||||||
| chr18:49564442 | T | C | 3 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0076g0065 |
4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-875T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564442 | |||||||
| chr18:49564551 | C | A | 1 | a0001c0001t0077g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.98-766C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564551 | |||||||
| chr18:49564659 | A | C | 1 | a0001c0001t0011g0266 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.98-658A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564659 | |||||||
| chr18:49564858 | C | T | 1 | a0002c0002t0064g0350 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.98-459C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564858 | |||||||
| chr18:49564915 | C | T | 14 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0026g0259 others(11): Show |
15 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.98-402C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564915 | |||||||
| chr18:49564989 | C | T | 16 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0026g0259 others(13): Show |
18 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.98-328C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564989 | |||||||
| chr18:49564996 | C | T | 1 | a0001c0001t0085g0254 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.98-321C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49564996 | |||||||
| chr18:49565037 | T | C | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.98-280T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49565037 | |||||||
| chr18:49565147 | A | G | 16 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0026g0259 others(13): Show |
18 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.98-170A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49565147 | |||||||
| chr18:49565207 | G | A | 3 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0076g0065 |
4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-110G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49565207 | |||||||
| chr18:49565258 | C | T | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.98-59C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 1/9 | chr18 | 49565258 | |||||||
| chr18:49565605 | C | G | 4 | a0002c0002t0004g0311 a0002c0002t0023g0312 a0002c0002t0069g0313 others(1): Show |
4 | NA18962.hp1 NA19055.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+107C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49565605 | |||||||
| chr18:49565820 | G | T | 1 | a0001c0001t0003g0253 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.279+322G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49565820 | |||||||
| chr18:49565958 | A | G | 3 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0036g0250 |
3 | NA18975.hp1 NA18982.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.279+460A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49565958 | |||||||
| chr18:49566007 | G | A | 1 | a0001c0001t0006g0054 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.279+509G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566007 | |||||||
| chr18:49566100 | T | G | 5 | a0002c0002t0014g0022 a0002c0002t0014g0314 a0002c0002t0014g0315 others(2): Show |
6 | HG02109.hp2 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+602T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566100 | |||||||
| chr18:49566109 | A | G | 2 | a0001c0001t0084g0249 a0001c0001t0085g0254 |
2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.279+611A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566109 | |||||||
| chr18:49566138 | C | G | 2 | a0001c0001t0094g0050 a0001c0001t0096g0049 |
2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.279+640C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566138 | |||||||
| chr18:49566157 | A | AC | 2 | a0002c0002t0021g0025 a0002c0002t0021g0349 |
3 | HG01167.hp1 HG01346.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.279+660dupC | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | 49566157 | ||||||
| chr18:49566256 | G | A | 1 | a0001c0001t0044g0055 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.279+758G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566256 | |||||||
| chr18:49566450 | C | T | 2 | a0001c0001t0002g0247 a0001c0001t0092g0248 |
2 | HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.279+952C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566450 | |||||||
| chr18:49566493 | T | C | 3 | a0001c0001t0049g0281 a0001c0001t0097g0256 a0001c0001t0098g0257 |
3 | NA18944.hp2 NA19030.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.280-949T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566493 | |||||||
| chr18:49566500 | C | G | 1 | a0004c0010t0010g0246 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.280-942C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566500 | |||||||
| chr18:49566556 | G | T | 1 | a0001c0001t0049g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-886G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566556 | |||||||
| chr18:49566761 | A | G | 3 | a0001c0001t0033g0264 a0001c0001t0033g0265 a0001c0001t0083g0263 |
3 | HG00738.hp1 HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.280-681A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566761 | |||||||
| chr18:49566811 | A | G | 1 | a0001c0001t0025g0245 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280-631A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566811 | |||||||
| chr18:49566942 | G | A | 16 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0026g0259 others(13): Show |
18 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.280-500G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566942 | |||||||
| chr18:49566967 | G | A | 1 | a0001c0001t0049g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-475G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566967 | |||||||
| chr18:49566992 | T | G | 1 | a0002c0002t0005g0320 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.280-450T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49566992 | |||||||
| chr18:49567012 | G | T | 1 | a0001c0001t0089g0244 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.280-430G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49567012 | |||||||
| chr18:49567074 | C | T | 11 | a0001c0001t0003g0061 a0001c0001t0006g0007 a0001c0001t0006g0054 others(8): Show |
12 | HG00099.hp2 HG00733.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.280-368C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49567074 | |||||||
| chr18:49567107 | T | C | 2 | a0001c0001t0006g0057 a0001c0001t0006g0058 |
2 | HG02132.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.280-335T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49567107 | |||||||
| chr18:49567309 | C | T | 1 | a0001c0001t0011g0028 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280-133C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49567309 | |||||||
| chr18:49567420 | C | T | 256 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0172 others(253): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.280-22C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 2/9 | chr18 | 49567420 | |||||||
| chr18:49567866 | T | C | 2 | a0001c0001t0012g0066 a0001c0001t0127g0067 |
2 | HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.459+245T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49567866 | |||||||
| chr18:49567979 | TGAAGCAT others(18): Show |
T | 3 | a0001c0001t0015g0006 a0001c0001t0015g0047 a0001c0001t0015g0048 |
4 | HG00642.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+361_459+385del others(25): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr18 | 49567979 | ||||||
| chr18:49568052 | T | C | 256 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(253): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.459+431T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568052 | |||||||
| chr18:49568072 | C | T | 32 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(29): Show |
33 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.459+451C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568072 | |||||||
| chr18:49568157 | G | A | 2 | a0002c0002t0005g0023 a0002c0002t0051g0023 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.459+536G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568157 | |||||||
| chr18:49568175 | C | G | 17 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0026g0259 others(14): Show |
19 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.459+554C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568175 | |||||||
| chr18:49568413 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.459+792C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568413 | |||||||
| chr18:49568434 | G | A | 9 | a0001c0001t0002g0072 a0001c0001t0003g0070 a0001c0001t0003g0074 others(6): Show |
9 | HG02040.hp1 HG02080.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.459+813G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568434 | |||||||
| chr18:49568479 | C | T | 1 | a0001c0001t0017g0279 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.459+858C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568479 | |||||||
| chr18:49568512 | C | A | 1 | a0001c0001t0006g0059 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.459+891C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568512 | |||||||
| chr18:49568872 | CCTAAGCT others(3): Show |
C | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.460-561_460-552del others(10): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr18 | 49568872 | ||||||
| chr18:49568883 | C | G | 1 | a0001c0001t0077g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460-554C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568883 | |||||||
| chr18:49568928 | C | CA | 4 | a0001c0001t0026g0259 a0001c0001t0048g0260 a0001c0001t0081g0258 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-508dupA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr18 | 49568928 | ||||||
| chr18:49568956 | C | A | 12 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0026g0259 others(9): Show |
13 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.460-481C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49568956 | |||||||
| chr18:49569050 | A | G | 257 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(254): Show |
276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.460-387A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49569050 | |||||||
| chr18:49569117 | T | C | 169 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(166): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.460-320T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49569117 | |||||||
| chr18:49569204 | C | G | 12 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0026g0259 others(9): Show |
13 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.460-233C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49569204 | |||||||
| chr18:49569210 | C | T | 1 | a0002c0002t0073g0345 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.460-227C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49569210 | |||||||
| chr18:49569225 | T | C | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.460-212T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49569225 | |||||||
| chr18:49569305 | G | T | 1 | a0001c0001t0019g0240 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.460-132G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 3/9 | chr18 | 49569305 | |||||||
| chr18:49569606 | C | T | 13 | a0001c0001t0026g0259 a0001c0001t0033g0264 a0001c0001t0033g0265 others(10): Show |
13 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.571+58C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569606 | |||||||
| chr18:49569646 | G | A | 38 | a0001c0001t0102g0142 a0001c0001t0106g0143 a0002c0002t0005g0001 others(35): Show |
45 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.571+98G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569646 | |||||||
| chr18:49569705 | C | CT | 81 | a0001c0001t0003g0138 a0001c0001t0003g0139 a0001c0001t0018g0140 others(78): Show |
91 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.571+171dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49569705 | ||||||
| chr18:49569733 | G | A | 1 | a0002c0002t0028g0321 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.571+185G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569733 | |||||||
| chr18:49569829 | G | A | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.571+281G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569829 | |||||||
| chr18:49569868 | C | G | 1 | a0001c0001t0079g0278 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571+320C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569868 | |||||||
| chr18:49569924 | G | A | 28 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(25): Show |
29 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.571+376G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569924 | |||||||
| chr18:49569948 | G | A | 4 | a0003c0004t0016g0144 a0003c0004t0016g0145 a0003c0004t0016g0147 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.571+400G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49569948 | |||||||
| chr18:49570131 | G | C | 24 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0001t0010g0150 others(21): Show |
25 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.571+583G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570131 | |||||||
| chr18:49570145 | G | A | 1 | a0001c0001t0086g0262 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.571+597G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570145 | |||||||
| chr18:49570169 | G | A | 1 | a0001c0001t0120g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.571+621G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570169 | |||||||
| chr18:49570215 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.571+667G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570215 | |||||||
| chr18:49570221 | A | G | 24 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0001t0010g0150 others(21): Show |
25 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.571+673A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570221 | |||||||
| chr18:49570381 | T | TTAATGGT others(21): Show |
1 | a0002c0013t0004g0310 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.571+836_571+863dup others(28): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49570381 | ||||||
| chr18:49570612 | C | T | 62 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(59): Show |
66 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.571+1064C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570612 | |||||||
| chr18:49570698 | G | A | 1 | a0002c0002t0130g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.571+1150G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570698 | |||||||
| chr18:49570826 | C | CTCAAAAA others(16): Show |
1 | a0002c0012t0057g0341 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.571+1279_571+1301d others(25): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49570826 | ||||||
| chr18:49570876 | C | T | 1 | a0001c0001t0129g0137 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.571+1328C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570876 | |||||||
| chr18:49570921 | T | C | 8 | a0001c0001t0011g0009 a0001c0001t0011g0027 a0001c0001t0011g0028 others(5): Show |
9 | HG01109.hp1 HG01192.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.571+1373T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49570921 | |||||||
| chr18:49571002 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0201 a0001c0001t0001g0202 others(6): Show |
10 | HG00280.hp1 HG00323.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.571+1454G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571002 | |||||||
| chr18:49571028 | A | G | 28 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(25): Show |
29 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.571+1480A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571028 | |||||||
| chr18:49571051 | C | G | 1 | a0001c0011t0068g0351 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.571+1503C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571051 | |||||||
| chr18:49571119 | C | T | 153 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(150): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.571+1571C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571119 | |||||||
| chr18:49571193 | A | T | 4 | a0001c0001t0026g0259 a0001c0001t0048g0260 a0001c0001t0081g0258 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.571+1645A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571193 | |||||||
| chr18:49571205 | T | C | 28 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(25): Show |
29 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.571+1657T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571205 | |||||||
| chr18:49571212 | A | G | 1 | a0002c0002t0005g0344 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.571+1664A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571212 | |||||||
| chr18:49571241 | G | A | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.571+1693G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571241 | |||||||
| chr18:49571254 | G | T | 1 | a0001c0011t0068g0351 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.571+1706G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571254 | |||||||
| chr18:49571313 | T | C | 28 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(25): Show |
29 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.571+1765T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571313 | |||||||
| chr18:49571456 | A | G | 1 | a0001c0001t0003g0077 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.571+1908A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571456 | |||||||
| chr18:49571463 | C | G | 1 | a0001c0001t0003g0077 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.571+1915C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571463 | |||||||
| chr18:49571476 | T | A | 1 | a0001c0011t0068g0351 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.571+1928T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571476 | |||||||
| chr18:49571483 | T | C | 13 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(10): Show |
13 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.571+1935T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571483 | |||||||
| chr18:49571558 | A | G | 1 | a0001c0001t0061g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.571+2010A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571558 | |||||||
| chr18:49571693 | G | A | 8 | a0001c0001t0006g0030 a0001c0001t0038g0045 a0001c0001t0038g0169 others(5): Show |
8 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.571+2145G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571693 | |||||||
| chr18:49571702 | A | C | 4 | a0001c0001t0033g0264 a0001c0001t0033g0265 a0001c0001t0083g0263 others(1): Show |
4 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.571+2154A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571702 | |||||||
| chr18:49571866 | G | C | 1 | a0001c0001t0052g0347 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.571+2318G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571866 | |||||||
| chr18:49571873 | GAGAGAAG others(11): Show |
G | 1 | a0002c0012t0057g0341 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.571+2328_571+2345d others(20): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49571873 | ||||||
| chr18:49571899 | A | G | 1 | a0001c0001t0010g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.571+2351A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571899 | |||||||
| chr18:49571918 | G | C | 2 | a0002c0002t0004g0287 a0002c0002t0004g0288 |
2 | NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.571+2370G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571918 | |||||||
| chr18:49571986 | T | C | 3 | a0002c0002t0021g0025 a0002c0002t0021g0349 a0002c0002t0054g0322 |
4 | HG01167.hp1 HG01346.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.571+2438T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49571986 | |||||||
| chr18:49572031 | C | T | 17 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0001t0010g0150 others(14): Show |
18 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.571+2483C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572031 | |||||||
| chr18:49572112 | G | A | 1 | a0001c0001t0011g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.571+2564G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572112 | |||||||
| chr18:49572158 | A | G | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.571+2610A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572158 | |||||||
| chr18:49572248 | A | G | 1 | a0001c0001t0003g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.571+2700A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572248 | |||||||
| chr18:49572256 | GT | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0206 a0001c0001t0027g0207 |
4 | NA18960.hp2 NA18964.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.571+2710delT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572256 | ||||||
| chr18:49572276 | C | T | 9 | a0001c0001t0032g0041 a0001c0001t0032g0042 a0003c0004t0016g0144 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.571+2728C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572276 | |||||||
| chr18:49572320 | CAAAAATA | C | 63 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(60): Show |
67 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.571+2792_571+2798d others(9): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572320 | ||||||
| chr18:49572333 | T | A | 1 | a0001c0001t0003g0077 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.571+2785T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572333 | |||||||
| chr18:49572333 | TAAAA | T | 25 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0001t0010g0150 others(22): Show |
27 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.571+2788_571+2791d others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572333 | ||||||
| chr18:49572361 | A | G | 2 | a0001c0001t0084g0249 a0001c0001t0085g0254 |
2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.571+2813A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572361 | |||||||
| chr18:49572370 | A | G | 1 | a0001c0001t0017g0277 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.571+2822A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572370 | |||||||
| chr18:49572386 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0019g0239 |
2 | NA18968.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.571+2838A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572386 | |||||||
| chr18:49572422 | C | A | 1 | a0001c0001t0012g0083 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.571+2874C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572422 | |||||||
| chr18:49572490 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.572-2879A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572490 | |||||||
| chr18:49572714 | G | C | 39 | a0001c0001t0102g0142 a0001c0001t0106g0143 a0002c0002t0005g0001 others(36): Show |
46 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.572-2655G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572714 | |||||||
| chr18:49572730 | T | TA | 7 | a0001c0001t0003g0077 a0001c0001t0003g0084 a0001c0001t0003g0138 others(4): Show |
7 | HG00140.hp2 HG03654.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.572-2617dupA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572730 | ||||||
| chr18:49572730 | TA | T | 22 | a0001c0001t0001g0208 a0001c0001t0002g0013 a0001c0001t0002g0134 others(19): Show |
22 | HG00609.hp1 HG01975.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.572-2617delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572730 | ||||||
| chr18:49572730 | TAA | T | 187 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(184): Show |
203 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.572-2618_572-2617d others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572730 | ||||||
| chr18:49572730 | TAAA | T | 41 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(38): Show |
43 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.572-2619_572-2617d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572730 | ||||||
| chr18:49572730 | TAAAA | T | 15 | a0001c0001t0010g0150 a0001c0001t0010g0151 a0001c0001t0010g0154 others(12): Show |
16 | HG00639.hp2 HG00735.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.572-2620_572-2617d others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572730 | ||||||
| chr18:49572814 | T | TTACATGT others(16): Show |
1 | a0001c0001t0011g0078 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.572-2553_572-2531d others(25): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49572814 | ||||||
| chr18:49572816 | A | G | 35 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0001t0010g0150 others(32): Show |
38 | HG00639.hp2 HG00735.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.572-2553A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572816 | |||||||
| chr18:49572831 | T | C | 1 | a0001c0001t0135g0211 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.572-2538T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49572831 | |||||||
| chr18:49573024 | G | T | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.572-2345G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573024 | |||||||
| chr18:49573073 | C | G | 1 | a0001c0001t0049g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.572-2296C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573073 | |||||||
| chr18:49573184 | T | G | 1 | a0001c0001t0084g0249 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.572-2185T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573184 | |||||||
| chr18:49573287 | G | T | 1 | a0001c0001t0006g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.572-2082G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573287 | |||||||
| chr18:49573294 | C | G | 3 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 |
3 | NA18990.hp1 NA19004.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.572-2075C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573294 | |||||||
| chr18:49573302 | G | GGTTGTCG others(6): Show |
1 | a0001c0001t0001g0068 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.572-2063_572-2051d others(15): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49573302 | ||||||
| chr18:49573304 | T | C | 10 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0026g0259 others(7): Show |
11 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.572-2065T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573304 | |||||||
| chr18:49573309 | G | A | 3 | a0001c0001t0027g0231 a0001c0001t0138g0212 a0002c0002t0067g0309 |
3 | NA18947.hp2 NA18948.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.572-2060G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573309 | |||||||
| chr18:49573326 | C | G | 1 | a0001c0001t0082g0261 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.572-2043C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573326 | |||||||
| chr18:49573329 | A | G | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.572-2040A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573329 | |||||||
| chr18:49573355 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.572-2014G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573355 | |||||||
| chr18:49573491 | A | C | 17 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(14): Show |
17 | HG00738.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.572-1878A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573491 | |||||||
| chr18:49573512 | G | A | 1 | a0001c0001t0095g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.572-1857G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573512 | |||||||
| chr18:49573572 | T | A | 1 | a0002c0002t0004g0289 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.572-1797T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573572 | |||||||
| chr18:49573576 | A | T | 25 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0001t0010g0150 others(22): Show |
27 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.572-1793A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573576 | |||||||
| chr18:49573579 | C | CA | 6 | a0001c0001t0001g0068 a0001c0001t0011g0266 a0001c0001t0015g0047 others(3): Show |
6 | HG01981.hp1 NA18944.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.572-1777dupA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49573579 | ||||||
| chr18:49573579 | CA | C | 8 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(5): Show |
9 | HG02559.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.572-1777delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr18 | 49573579 | ||||||
| chr18:49573644 | C | T | 1 | a0001c0001t0015g0006 | 2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.572-1725C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573644 | |||||||
| chr18:49573793 | A | C | 23 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0026g0259 others(20): Show |
25 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.572-1576A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573793 | |||||||
| chr18:49573915 | G | T | 75 | a0001c0001t0018g0140 a0001c0001t0077g0051 a0001c0001t0102g0142 others(72): Show |
84 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.572-1454G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573915 | |||||||
| chr18:49573928 | G | A | 3 | a0001c0001t0013g0132 a0001c0001t0018g0085 a0001c0001t0018g0131 |
3 | HG00609.hp1 NA18971.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.572-1441G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49573928 | |||||||
| chr18:49574093 | C | T | 6 | a0001c0001t0003g0077 a0001c0001t0003g0082 a0001c0001t0003g0084 others(3): Show |
6 | NA18941.hp2 NA18968.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.572-1276C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574093 | |||||||
| chr18:49574235 | GGCACTCA others(4): Show |
G | 1 | a0001c0001t0010g0148 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.572-1133_572-1123d others(13): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574235 | |||||||
| chr18:49574293 | C | T | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.572-1076C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574293 | |||||||
| chr18:49574429 | C | T | 7 | a0001c0001t0026g0259 a0001c0001t0048g0260 a0001c0001t0081g0258 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.572-940C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574429 | |||||||
| chr18:49574456 | G | A | 2 | a0001c0001t0015g0043 a0001c0001t0015g0044 |
2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.572-913G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574456 | |||||||
| chr18:49574670 | A | T | 74 | a0001c0001t0018g0140 a0001c0001t0077g0051 a0001c0001t0102g0142 others(71): Show |
83 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.572-699A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574670 | |||||||
| chr18:49574880 | G | A | 3 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0076g0065 |
4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-489G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574880 | |||||||
| chr18:49574977 | G | T | 1 | a0002c0013t0004g0310 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.572-392G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49574977 | |||||||
| chr18:49575061 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.572-308T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49575061 | |||||||
| chr18:49575219 | T | C | 13 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0001t0010g0150 others(10): Show |
14 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.572-150T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49575219 | |||||||
| chr18:49575235 | T | G | 3 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0076g0065 |
4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-134T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49575235 | |||||||
| chr18:49575284 | C | T | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.572-85C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49575284 | |||||||
| chr18:49575326 | G | A | 1 | a0001c0001t0017g0274 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.572-43G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 4/9 | chr18 | 49575326 | |||||||
| chr18:49575598 | C | A | 1 | a0001c0001t0001g0213 | 1 | HG02523.hp1 | splice_region_variant&intron_variant | LOW | c.793+8C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575598 | |||||||
| chr18:49575632 | T | C | 188 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(185): Show |
203 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.793+42T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575632 | |||||||
| chr18:49575673 | G | A | 2 | a0002c0002t0005g0324 a0002c0002t0005g0338 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.793+83G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575673 | |||||||
| chr18:49575732 | A | G | 259 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(256): Show |
278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.793+142A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575732 | |||||||
| chr18:49575747 | C | T | 6 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.793+157C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575747 | |||||||
| chr18:49575817 | ATTTCT | A | 73 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(70): Show |
77 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.793+241_793+245del others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49575817 | ||||||
| chr18:49575833 | T | C | 1 | a0001c0001t0128g0060 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.793+243T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575833 | |||||||
| chr18:49575841 | C | CT | 13 | a0001c0001t0001g0068 a0001c0001t0006g0109 a0001c0001t0012g0083 others(10): Show |
13 | HG00140.hp2 HG01168.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.793+265dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49575841 | ||||||
| chr18:49575853 | T | A | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+263T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575853 | |||||||
| chr18:49575945 | T | A | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+355T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575945 | |||||||
| chr18:49575986 | G | A | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+396G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49575986 | |||||||
| chr18:49576037 | C | T | 3 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0076g0065 |
4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+447C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576037 | |||||||
| chr18:49576127 | C | T | 1 | a0001c0001t0048g0260 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.793+537C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576127 | |||||||
| chr18:49576128 | G | A | 2 | a0001c0001t0012g0066 a0001c0001t0127g0067 |
2 | HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.793+538G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576128 | |||||||
| chr18:49576133 | C | T | 77 | a0001c0001t0018g0085 a0001c0001t0018g0131 a0001c0001t0018g0140 others(74): Show |
86 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.793+543C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576133 | |||||||
| chr18:49576223 | C | T | 1 | a0001c0001t0037g0135 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.793+633C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576223 | |||||||
| chr18:49576272 | A | G | 4 | a0001c0001t0026g0259 a0001c0001t0048g0260 a0001c0001t0081g0258 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+682A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576272 | |||||||
| chr18:49576332 | T | C | 3 | a0001c0001t0032g0041 a0001c0001t0032g0042 a0001c0001t0049g0281 |
3 | HG01891.hp2 HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.793+742T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576332 | |||||||
| chr18:49576338 | A | C | 1 | a0002c0012t0057g0341 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.793+748A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576338 | |||||||
| chr18:49576339 | A | G | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.793+749A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576339 | |||||||
| chr18:49576428 | CTTTTCTT others(4): Show |
C | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+840_793+850del others(11): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576428 | ||||||
| chr18:49576433 | CT | C | 5 | a0001c0001t0003g0077 a0001c0001t0102g0142 a0002c0002t0067g0309 others(2): Show |
5 | HG01257.hp2 HG02602.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+850delT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576433 | ||||||
| chr18:49576457 | C | CT | 54 | a0001c0001t0001g0214 a0001c0001t0002g0053 a0001c0001t0002g0106 others(51): Show |
54 | HG00140.hp2 HG00438.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.793+894dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | C | CTT | 46 | a0001c0001t0001g0017 a0001c0001t0001g0068 a0001c0001t0001g0172 others(43): Show |
49 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.793+893_793+894dup others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | C | CTTT | 25 | a0001c0001t0001g0018 a0001c0001t0001g0204 a0001c0001t0001g0205 others(22): Show |
26 | HG00438.hp1 HG00642.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.793+892_793+894dup others(3): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | C | CTTTT | 13 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(10): Show |
13 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.793+891_793+894dup others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | C | CTTTTT | 20 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(17): Show |
21 | HG00735.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.793+890_793+894dup others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | C | CTTTTTT | 13 | a0001c0001t0003g0038 a0001c0001t0006g0030 a0001c0001t0008g0016 others(10): Show |
15 | HG01069.hp2 HG01071.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.793+889_793+894dup others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | C | CTTTTTTT | 8 | a0001c0001t0006g0057 a0001c0001t0008g0187 a0001c0001t0008g0188 others(5): Show |
8 | HG00544.hp2 HG01261.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.793+888_793+894dup others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | C | CTTTTTTT others(1): Show |
12 | a0001c0001t0003g0061 a0001c0001t0006g0007 a0001c0001t0008g0191 others(9): Show |
13 | HG00099.hp2 HG00423.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.793+887_793+894dup others(8): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | C | CTTTTTTT others(2): Show |
8 | a0001c0001t0006g0058 a0001c0001t0006g0059 a0001c0001t0006g0062 others(5): Show |
9 | HG01074.hp1 HG01109.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.793+886_793+894dup others(9): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0020g0348 a0001c0001t0044g0055 a0001c0001t0115g0063 others(2): Show |
5 | HG00733.hp1 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+885_793+894dup others(10): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | C | CTTTTTTT others(5): Show |
1 | a0006c0008t0008g0284 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.793+883_793+894dup others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0006g0054 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.793+882_793+894dup others(13): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | CTTTTTT | C | 7 | a0001c0001t0041g0158 a0001c0001t0097g0256 a0001c0001t0098g0257 others(4): Show |
7 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.793+889_793+894del others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | CTTTTTTT others(3): Show |
C | 9 | a0001c0001t0018g0140 a0002c0002t0005g0324 a0002c0002t0009g0334 others(6): Show |
9 | HG00140.hp1 HG01071.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.793+885_793+894del others(10): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | CTTTTTTT others(4): Show |
C | 67 | a0001c0001t0018g0085 a0001c0001t0018g0131 a0001c0001t0077g0051 others(64): Show |
76 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.793+884_793+894del others(11): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0014g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.793+883_793+894del others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576457 | CTTTTTTT others(8): Show |
C | 10 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0026g0259 others(7): Show |
11 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.793+880_793+894del others(15): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576457 | ||||||
| chr18:49576531 | G | A | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+941G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576531 | |||||||
| chr18:49576532 | A | C | 4 | a0002c0002t0005g0320 a0002c0002t0005g0324 a0002c0002t0005g0338 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+942A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576532 | |||||||
| chr18:49576627 | C | A | 76 | a0001c0001t0018g0085 a0001c0001t0018g0131 a0001c0001t0018g0140 others(73): Show |
85 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.793+1037C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576627 | |||||||
| chr18:49576628 | C | A | 1 | a0002c0013t0004g0310 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.793+1038C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576628 | |||||||
| chr18:49576783 | T | C | 2 | a0002c0002t0004g0343 a0002c0002t0065g0342 |
2 | HG02155.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.793+1193T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576783 | |||||||
| chr18:49576836 | T | TCCTGGGC others(12): Show |
1 | a0002c0012t0057g0341 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.793+1251_793+1269d others(21): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49576836 | ||||||
| chr18:49576846 | A | C | 2 | a0001c0001t0094g0050 a0001c0001t0096g0049 |
2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.793+1256A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576846 | |||||||
| chr18:49576908 | T | G | 6 | a0001c0001t0010g0150 a0001c0001t0010g0154 a0001c0001t0010g0155 others(3): Show |
7 | HG03017.hp2 HG03654.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.793+1318T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49576908 | |||||||
| chr18:49577012 | T | TTTTATTT others(2): Show |
2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+1425_793+1426i others(11): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577012 | ||||||
| chr18:49577022 | A | T | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+1432A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577022 | |||||||
| chr18:49577024 | T | A | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+1434T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577024 | |||||||
| chr18:49577025 | T | A | 16 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(13): Show |
16 | HG00738.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.793+1435T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577025 | |||||||
| chr18:49577026 | A | T | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+1436A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577026 | |||||||
| chr18:49577030 | T | A | 22 | a0001c0001t0001g0201 a0001c0001t0003g0061 a0001c0001t0006g0007 others(19): Show |
23 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.793+1440T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577030 | |||||||
| chr18:49577030 | T | TTTTTTTA others(17): Show |
1 | a0001c0001t0010g0148 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.793+1444_793+1467d others(26): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577030 | ||||||
| chr18:49577099 | A | T | 36 | a0001c0001t0018g0085 a0001c0001t0018g0131 a0001c0001t0018g0140 others(33): Show |
38 | HG00558.hp2 HG00609.hp2 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.793+1509A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577099 | |||||||
| chr18:49577162 | T | C | 258 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(255): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.793+1572T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577162 | |||||||
| chr18:49577189 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.793+1599A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577189 | |||||||
| chr18:49577190 | T | G | 1 | a0001c0001t0001g0238 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.793+1600T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577190 | |||||||
| chr18:49577239 | C | T | 1 | a0001c0001t0010g0149 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.793+1649C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577239 | |||||||
| chr18:49577259 | C | T | 1 | a0001c0001t0003g0076 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.793+1669C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577259 | |||||||
| chr18:49577324 | A | G | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.793+1734A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577324 | |||||||
| chr18:49577455 | C | CT | 3 | a0001c0001t0025g0245 a0001c0001t0026g0259 a0001c0001t0048g0260 |
3 | HG01243.hp2 HG01884.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.793+1869dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577455 | ||||||
| chr18:49577479 | C | T | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.793+1889C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577479 | |||||||
| chr18:49577491 | G | A | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.793+1901G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577491 | |||||||
| chr18:49577501 | T | C | 1 | a0004c0006t0029g0019 | 2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+1911T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577501 | |||||||
| chr18:49577507 | T | C | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.793+1917T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577507 | |||||||
| chr18:49577513 | G | T | 6 | a0001c0001t0003g0033 a0001c0001t0003g0037 a0001c0001t0006g0030 others(3): Show |
6 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.793+1923G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577513 | |||||||
| chr18:49577528 | C | T | 1 | a0001c0001t0044g0229 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.793+1938C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577528 | |||||||
| chr18:49577546 | C | CG | 17 | a0001c0001t0001g0068 a0001c0001t0001g0273 a0001c0001t0002g0106 others(14): Show |
17 | HG01346.hp1 HG01361.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.793+1960dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577546 | ||||||
| chr18:49577546 | C | T | 2 | a0001c0001t0038g0045 a0001c0001t0038g0169 |
2 | HG02071.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.793+1956C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577546 | |||||||
| chr18:49577592 | G | A | 2 | a0001c0001t0084g0249 a0001c0001t0085g0254 |
2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.793+2002G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577592 | |||||||
| chr18:49577595 | C | CG | 5 | a0001c0001t0001g0068 a0001c0001t0011g0078 a0001c0001t0012g0083 others(2): Show |
5 | HG00140.hp2 HG01261.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+2008dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577595 | ||||||
| chr18:49577606 | A | G | 12 | a0001c0001t0032g0041 a0001c0001t0032g0042 a0001c0001t0041g0158 others(9): Show |
13 | HG01891.hp2 HG02055.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.793+2016A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577606 | |||||||
| chr18:49577616 | T | TCCC | 38 | a0001c0001t0018g0085 a0001c0001t0018g0131 a0001c0001t0018g0140 others(35): Show |
40 | HG00558.hp2 HG00609.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.793+2027_793+2029d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577616 | ||||||
| chr18:49577619 | C | CGGATGGG others(575): Show |
2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2032_793+2033i others(584): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577619 | ||||||
| chr18:49577619 | C | T | 1 | a0001c0001t0056g0285 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.793+2029C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577619 | |||||||
| chr18:49577619 | CGGACGGG others(318): Show |
C | 59 | a0001c0001t0003g0061 a0001c0001t0006g0007 a0001c0001t0006g0054 others(56): Show |
63 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.793+2116_793+2440d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577619 | ||||||
| chr18:49577624 | G | A | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2034G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577624 | |||||||
| chr18:49577624 | G | C | 18 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(15): Show |
18 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.793+2034G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577624 | |||||||
| chr18:49577625 | GGGCGGCT others(4): Show |
G | 1 | a0001c0001t0002g0251 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.793+2038_793+2048d others(13): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577625 | ||||||
| chr18:49577657 | CACCTCCC others(42): Show |
C | 18 | a0001c0001t0003g0033 a0001c0001t0003g0037 a0001c0001t0052g0347 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.793+2082_793+2130d others(51): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577657 | ||||||
| chr18:49577661 | T | C | 1 | a0001c0001t0048g0260 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.793+2071T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577661 | |||||||
| chr18:49577662 | C | A | 1 | a0001c0001t0048g0260 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.793+2072C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577662 | |||||||
| chr18:49577667 | C | T | 6 | a0003c0004t0016g0144 a0003c0004t0016g0145 a0003c0004t0016g0147 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.793+2077C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577667 | |||||||
| chr18:49577669 | G | C | 16 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(13): Show |
16 | HG00738.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.793+2079G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577669 | |||||||
| chr18:49577673 | G | A | 1 | a0001c0001t0012g0012 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.793+2083G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577673 | |||||||
| chr18:49577676 | ACGGCTGG others(141): Show |
A | 12 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.793+2096_793+2243d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577676 | ||||||
| chr18:49577677 | C | T | 1 | a0002c0002t0004g0004 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.793+2087C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577677 | |||||||
| chr18:49577683 | G | T | 8 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0026g0259 others(5): Show |
9 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.793+2093G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577683 | |||||||
| chr18:49577686 | A | G | 1 | a0002c0002t0021g0025 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.793+2096A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577686 | |||||||
| chr18:49577689 | CGGGGGGC others(43): Show |
C | 4 | a0001c0001t0038g0045 a0001c0001t0038g0169 a0001c0001t0094g0050 others(1): Show |
4 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+2116_793+2165d others(52): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577689 | ||||||
| chr18:49577700 | CCCCCCAA others(317): Show |
C | 1 | a0001c0005t0007g0179 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.793+2116_793+2439d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577700 | ||||||
| chr18:49577706 | A | C | 102 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(99): Show |
111 | HG00558.hp2 HG00609.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.793+2116A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577706 | |||||||
| chr18:49577724 | C | G | 1 | a0002c0002t0021g0025 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.793+2134C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577724 | |||||||
| chr18:49577725 | A | G | 4 | a0002c0002t0004g0300 a0002c0002t0018g0170 a0002c0002t0021g0025 others(1): Show |
4 | HG01167.hp1 HG02015.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+2135A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577725 | |||||||
| chr18:49577735 | G | A | 3 | a0001c0001t0097g0256 a0001c0001t0098g0257 a0002c0002t0021g0025 |
3 | HG01167.hp1 NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.793+2145G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577735 | |||||||
| chr18:49577738 | C | CG | 11 | a0001c0001t0002g0252 a0001c0001t0011g0027 a0001c0001t0012g0083 others(8): Show |
11 | HG00140.hp2 HG01175.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.793+2155dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577738 | ||||||
| chr18:49577738 | C | T | 1 | a0001c0001t0137g0092 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.793+2148C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577738 | |||||||
| chr18:49577739 | GGGGGGGC others(317): Show |
G | 1 | a0001c0001t0101g0186 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.793+2156_793+2479d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577739 | ||||||
| chr18:49577749 | AC | A | 94 | a0001c0001t0018g0085 a0001c0001t0018g0131 a0001c0001t0018g0140 others(91): Show |
104 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.793+2166delC | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577749 | ||||||
| chr18:49577768 | G | GGACACGG others(120): Show |
2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2180_793+2181i others(129): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577768 | ||||||
| chr18:49577771 | T | C | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2181T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577771 | |||||||
| chr18:49577785 | A | G | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2195A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577785 | |||||||
| chr18:49577788 | C | CG | 8 | a0001c0001t0001g0237 a0001c0001t0003g0035 a0001c0001t0003g0138 others(5): Show |
8 | HG01516.hp2 HG02602.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.793+2204dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577788 | ||||||
| chr18:49577791 | G | A | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2201G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577791 | |||||||
| chr18:49577798 | A | AC | 10 | a0001c0001t0001g0218 a0001c0001t0002g0106 a0001c0001t0003g0104 others(7): Show |
10 | HG00140.hp2 HG01243.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.793+2215dupC | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577798 | ||||||
| chr18:49577803 | C | G | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.793+2213C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577803 | |||||||
| chr18:49577805 | C | A | 1 | a0002c0013t0004g0310 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.793+2215C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577805 | |||||||
| chr18:49577810 | CCCTCCCG others(121): Show |
C | 2 | a0001c0001t0084g0249 a0001c0001t0085g0254 |
2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.793+2226_793+2353d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577810 | ||||||
| chr18:49577837 | T | C | 1 | a0001c0001t0076g0065 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.793+2247T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577837 | |||||||
| chr18:49577837 | T | TG | 16 | a0001c0001t0002g0002 a0001c0001t0002g0123 a0001c0001t0002g0251 others(13): Show |
16 | HG00140.hp2 HG00544.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.793+2254dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577837 | ||||||
| chr18:49577838 | G | A | 1 | a0001c0001t0076g0065 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.793+2248G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577838 | |||||||
| chr18:49577838 | G | C | 1 | a0002c0002t0005g0001 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.793+2248G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577838 | |||||||
| chr18:49577848 | A | AC | 12 | a0001c0001t0001g0237 a0001c0001t0002g0052 a0001c0001t0002g0252 others(9): Show |
12 | HG01099.hp2 HG01175.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.793+2265dupC | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577848 | ||||||
| chr18:49577906 | C | T | 2 | a0002c0002t0005g0324 a0002c0002t0005g0338 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.793+2316C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577906 | |||||||
| chr18:49577908 | AGTAGGGG others(228): Show |
A | 2 | a0002c0002t0005g0324 a0002c0002t0005g0338 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.793+2320_793+2554d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577908 | ||||||
| chr18:49577916 | T | C | 126 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(123): Show |
137 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.793+2326T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577916 | |||||||
| chr18:49577949 | G | C | 56 | a0001c0001t0003g0061 a0001c0001t0006g0007 a0001c0001t0006g0054 others(53): Show |
60 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.793+2359G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577949 | |||||||
| chr18:49577954 | G | A | 61 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(58): Show |
65 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.793+2364G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577954 | |||||||
| chr18:49577961 | C | T | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2371C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577961 | |||||||
| chr18:49577975 | AC | A | 12 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.793+2392delC | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49577975 | ||||||
| chr18:49577976 | C | T | 16 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(13): Show |
16 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.793+2386C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577976 | |||||||
| chr18:49577982 | C | A | 3 | a0001c0001t0032g0041 a0001c0001t0032g0042 a0001c0001t0049g0281 |
3 | HG01891.hp2 HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.793+2392C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577982 | |||||||
| chr18:49577991 | C | T | 16 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(13): Show |
16 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.793+2401C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49577991 | |||||||
| chr18:49578003 | G | T | 1 | a0001c0001t0044g0229 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.793+2413G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578003 | |||||||
| chr18:49578051 | C | T | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.793+2461C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578051 | |||||||
| chr18:49578063 | C | CG | 11 | a0001c0001t0001g0237 a0001c0001t0002g0122 a0001c0001t0003g0127 others(8): Show |
11 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.793+2480dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578063 | ||||||
| chr18:49578063 | C | T | 1 | a0001c0001t0056g0285 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.793+2473C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578063 | |||||||
| chr18:49578069 | G | T | 3 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0076g0065 |
4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+2479G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578069 | |||||||
| chr18:49578074 | G | A | 5 | a0001c0001t0032g0041 a0001c0001t0032g0042 a0001c0001t0049g0281 others(2): Show |
6 | HG01891.hp2 HG02055.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.793+2484G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578074 | |||||||
| chr18:49578109 | G | A | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2519G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578109 | |||||||
| chr18:49578112 | C | CG | 10 | a0001c0001t0001g0205 a0001c0001t0001g0237 a0001c0001t0001g0273 others(7): Show |
10 | HG00140.hp1 HG02056.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.793+2528dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578112 | ||||||
| chr18:49578122 | AC | A | 248 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(245): Show |
267 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.793+2541delC | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578122 | ||||||
| chr18:49578146 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.793+2556C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578146 | |||||||
| chr18:49578163 | G | A | 1 | a0002c0002t0054g0322 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.793+2573G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578163 | |||||||
| chr18:49578168 | C | T | 1 | a0001c0001t0049g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.793+2578C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578168 | |||||||
| chr18:49578174 | T | G | 1 | a0001c0003t0045g0196 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.793+2584T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578174 | |||||||
| chr18:49578178 | C | T | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2588C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578178 | |||||||
| chr18:49578245 | A | G | 1 | a0001c0003t0045g0196 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.793+2655A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578245 | |||||||
| chr18:49578249 | G | A | 1 | a0001c0001t0126g0079 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.793+2659G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578249 | |||||||
| chr18:49578252 | C | T | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.793+2662C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578252 | |||||||
| chr18:49578306 | C | G | 1 | a0001c0001t0044g0055 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.793+2716C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578306 | |||||||
| chr18:49578312 | A | G | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2722A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578312 | |||||||
| chr18:49578315 | C | CG | 7 | a0001c0001t0001g0068 a0001c0001t0002g0126 a0001c0001t0002g0251 others(4): Show |
7 | HG01192.hp2 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.793+2728dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578315 | ||||||
| chr18:49578325 | C | T | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2735C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578325 | |||||||
| chr18:49578335 | C | G | 1 | a0002c0002t0022g0302 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.793+2745C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578335 | |||||||
| chr18:49578343 | C | CG | 5 | a0001c0001t0008g0188 a0001c0001t0013g0087 a0001c0001t0046g0086 others(2): Show |
5 | HG01175.hp1 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+2757dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578343 | ||||||
| chr18:49578343 | C | G | 39 | a0001c0001t0102g0142 a0001c0001t0106g0143 a0002c0002t0005g0001 others(36): Show |
46 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.793+2753C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578343 | |||||||
| chr18:49578351 | C | G | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2761C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578351 | |||||||
| chr18:49578352 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.793+2762G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578352 | |||||||
| chr18:49578366 | G | A | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2776G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578366 | |||||||
| chr18:49578391 | C | CG | 7 | a0001c0001t0001g0237 a0001c0001t0003g0104 a0001c0001t0003g0138 others(4): Show |
7 | HG01516.hp2 HG01978.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.793+2805dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578391 | ||||||
| chr18:49578403 | G | A | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793+2813G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578403 | |||||||
| chr18:49578440 | A | G | 1 | a0001c0001t0011g0078 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.793+2850A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578440 | |||||||
| chr18:49578481 | C | T | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.793+2891C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578481 | |||||||
| chr18:49578507 | C | T | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-2908C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578507 | |||||||
| chr18:49578508 | G | C | 1 | a0001c0001t0095g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.794-2907G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578508 | |||||||
| chr18:49578511 | C | T | 1 | a0001c0003t0121g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.794-2904C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578511 | |||||||
| chr18:49578512 | G | A | 2 | a0001c0001t0081g0258 a0001c0001t0082g0261 |
2 | HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.794-2903G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578512 | |||||||
| chr18:49578521 | C | T | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2894C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578521 | |||||||
| chr18:49578592 | G | A | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2823G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578592 | |||||||
| chr18:49578615 | T | C | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2800T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578615 | |||||||
| chr18:49578615 | T | TG | 15 | a0001c0001t0001g0068 a0001c0001t0001g0216 a0001c0001t0001g0223 others(12): Show |
15 | HG01109.hp2 HG01978.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.794-2796dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578615 | ||||||
| chr18:49578621 | G | A | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(2): Show |
5 | HG02572.hp1 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2794G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578621 | |||||||
| chr18:49578646 | C | G | 1 | a0001c0011t0068g0351 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.794-2769C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578646 | |||||||
| chr18:49578684 | T | G | 11 | a0001c0001t0003g0061 a0001c0001t0003g0138 a0001c0001t0006g0007 others(8): Show |
12 | HG00099.hp2 HG00733.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.794-2731T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578684 | |||||||
| chr18:49578698 | C | T | 1 | a0001c0001t0131g0268 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.794-2717C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578698 | |||||||
| chr18:49578736 | G | T | 1 | a0003c0004t0016g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.794-2679G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578736 | |||||||
| chr18:49578750 | G | C | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2665G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578750 | |||||||
| chr18:49578825 | G | A | 16 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(13): Show |
16 | HG00738.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.794-2590G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578825 | |||||||
| chr18:49578827 | C | T | 1 | a0002c0002t0005g0339 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.794-2588C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578827 | |||||||
| chr18:49578828 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.794-2587C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578828 | |||||||
| chr18:49578835 | A | T | 1 | a0001c0011t0068g0351 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.794-2580A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578835 | |||||||
| chr18:49578854 | C | G | 3 | a0002c0002t0004g0300 a0002c0002t0018g0170 a0002c0002t0130g0168 |
3 | HG02015.hp1 NA19067.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.794-2561C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578854 | |||||||
| chr18:49578881 | GCGTGCCT others(5): Show |
G | 74 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(71): Show |
78 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.794-2531_794-2520d others(14): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49578881 | ||||||
| chr18:49578886 | C | A | 5 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-2529C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578886 | |||||||
| chr18:49578894 | C | T | 3 | a0001c0001t0049g0281 a0001c0001t0097g0256 a0001c0001t0098g0257 |
3 | NA18944.hp2 NA19030.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.794-2521C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578894 | |||||||
| chr18:49578905 | G | T | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2510G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578905 | |||||||
| chr18:49578974 | T | C | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.794-2441T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578974 | |||||||
| chr18:49578983 | A | G | 1 | a0001c0001t0135g0211 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.794-2432A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49578983 | |||||||
| chr18:49579001 | G | GGGGAGA | 4 | a0001c0001t0001g0271 a0001c0001t0012g0141 a0001c0003t0007g0190 others(1): Show |
4 | HG01106.hp1 HG01106.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2182_794-2177d others(8): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAC others(33): Show |
1 | a0001c0001t0003g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.794-2408_794-2407i others(42): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAC others(41): Show |
1 | a0001c0001t0115g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.794-2408_794-2407i others(50): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAC others(17): Show |
1 | a0001c0001t0006g0058 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.794-2408_794-2407i others(26): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAC others(41): Show |
1 | a0001c0001t0044g0055 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.794-2408_794-2407i others(50): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAC others(143): Show |
1 | a0001c0001t0006g0057 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.794-2408_794-2407i others(152): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAC others(17): Show |
1 | a0001c0001t0006g0059 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.794-2408_794-2407i others(26): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAC others(41): Show |
2 | a0001c0001t0006g0007 a0001c0001t0006g0054 |
2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.794-2408_794-2407i others(50): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAC others(59): Show |
1 | a0001c0001t0129g0137 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.794-2408_794-2407i others(68): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAC others(54): Show |
1 | a0001c0001t0032g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.794-2408_794-2407i others(63): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(51): Show |
1 | a0001c0001t0001g0172 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.794-2407_794-2406i others(60): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(124): Show |
1 | a0002c0002t0064g0350 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.794-2406_794-2405i others(133): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(5): Show |
7 | a0001c0001t0001g0018 a0001c0001t0002g0112 a0001c0001t0002g0123 others(4): Show |
7 | HG02258.hp1 HG02896.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-2188_794-2177d others(14): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(35): Show |
1 | a0002c0002t0004g0289 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.794-2402_794-2401i others(44): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(53): Show |
1 | a0002c0002t0009g0334 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.794-2400_794-2399i others(62): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(11): Show |
5 | a0001c0001t0001g0270 a0001c0001t0010g0150 a0001c0001t0012g0003 others(2): Show |
5 | HG01070.hp1 HG02602.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2194_794-2177d others(20): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(17): Show |
8 | a0001c0001t0002g0002 a0001c0001t0002g0114 a0001c0001t0003g0035 others(5): Show |
8 | HG00544.hp1 HG00609.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.794-2200_794-2177d others(26): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(41): Show |
1 | a0001c0001t0019g0222 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.794-2386_794-2385i others(50): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(23): Show |
5 | a0001c0001t0003g0094 a0001c0001t0039g0177 a0001c0001t0047g0203 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-2206_794-2177d others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(29): Show |
13 | a0001c0001t0001g0236 a0001c0001t0002g0052 a0001c0001t0002g0126 others(10): Show |
13 | HG01099.hp2 HG01358.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.794-2212_794-2177d others(38): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(35): Show |
18 | a0001c0001t0001g0204 a0001c0001t0001g0217 a0001c0001t0001g0226 others(15): Show |
18 | HG01168.hp2 HG01258.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.794-2218_794-2177d others(44): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(41): Show |
16 | a0001c0001t0002g0013 a0001c0001t0003g0005 a0001c0001t0003g0031 others(13): Show |
16 | HG00639.hp1 HG00735.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.794-2224_794-2177d others(50): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(46): Show |
1 | a0001c0001t0013g0073 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.794-2364_794-2363i others(55): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(82): Show |
1 | a0002c0002t0014g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.794-2364_794-2363i others(91): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(47): Show |
13 | a0001c0001t0001g0214 a0001c0001t0001g0234 a0001c0001t0001g0235 others(10): Show |
13 | HG00323.hp2 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.794-2230_794-2177d others(56): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(53): Show |
12 | a0001c0001t0001g0215 a0001c0001t0002g0129 a0001c0001t0008g0194 others(9): Show |
13 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(10): Show |
intron_variant | MODIFIER | c.794-2236_794-2177d others(62): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(59): Show |
17 | a0001c0001t0001g0208 a0001c0001t0001g0228 a0001c0001t0001g0273 others(14): Show |
17 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.794-2242_794-2177d others(68): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(65): Show |
21 | a0001c0001t0001g0206 a0001c0001t0001g0213 a0001c0001t0001g0223 others(18): Show |
21 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.794-2248_794-2177d others(74): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(71): Show |
13 | a0001c0001t0002g0102 a0001c0001t0002g0122 a0001c0001t0002g0130 others(10): Show |
13 | HG00423.hp2 HG02056.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.794-2254_794-2177d others(80): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(77): Show |
17 | a0001c0001t0002g0002 a0001c0001t0002g0072 a0001c0001t0002g0124 others(14): Show |
17 | HG00741.hp2 HG01069.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.794-2260_794-2177d others(86): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(82): Show |
1 | a0002c0002t0005g0320 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.794-2328_794-2327i others(91): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(83): Show |
9 | a0001c0001t0001g0224 a0001c0001t0003g0253 a0001c0001t0012g0083 others(6): Show |
9 | HG00140.hp2 HG02165.hp2 HG04199.hp2 others(6): Show |
intron_variant | MODIFIER | c.794-2266_794-2177d others(92): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(89): Show |
9 | a0001c0001t0001g0018 a0001c0001t0001g0233 a0001c0001t0002g0053 others(6): Show |
10 | HG01496.hp2 HG01943.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.794-2272_794-2177d others(98): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(95): Show |
8 | a0001c0001t0006g0011 a0001c0001t0006g0097 a0001c0001t0011g0078 others(5): Show |
8 | HG00558.hp1 HG01496.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.794-2278_794-2177d others(104): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(101): Show |
5 | a0001c0001t0001g0220 a0001c0001t0008g0016 a0001c0001t0037g0089 others(2): Show |
6 | HG00438.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2284_794-2177d others(110): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(107): Show |
6 | a0001c0001t0010g0148 a0001c0001t0011g0009 a0001c0001t0015g0048 others(3): Show |
6 | HG00642.hp1 HG01433.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-2290_794-2177d others(116): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(113): Show |
9 | a0001c0001t0001g0201 a0001c0001t0003g0038 a0001c0001t0010g0155 others(6): Show |
9 | HG00280.hp1 HG01358.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.794-2296_794-2177d others(122): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(119): Show |
3 | a0001c0001t0002g0113 a0001c0001t0019g0239 a0001c0001t0140g0110 |
3 | HG00438.hp2 HG00738.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.794-2302_794-2177d others(128): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(125): Show |
4 | a0001c0001t0003g0101 a0001c0001t0019g0210 a0001c0001t0137g0092 others(1): Show |
4 | HG02300.hp1 NA18612.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2308_794-2177d others(134): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(131): Show |
3 | a0002c0002t0004g0305 a0002c0002t0022g0296 a0002c0002t0069g0313 |
3 | HG02155.hp2 NA18939.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.794-2314_794-2177d others(140): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(137): Show |
2 | a0001c0001t0002g0002 a0002c0002t0021g0025 |
2 | HG01167.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.794-2320_794-2177d others(146): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(149): Show |
2 | a0001c0001t0011g0009 a0002c0002t0059g0332 |
2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.794-2332_794-2177d others(158): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(155): Show |
1 | a0002c0002t0005g0001 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.794-2338_794-2177d others(164): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(167): Show |
1 | a0002c0002t0004g0300 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.794-2350_794-2177d others(176): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(24): Show |
1 | a0001c0001t0002g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794-2393_794-2392i others(33): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGAGAG others(78): Show |
1 | a0001c0001t0107g0185 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.794-2393_794-2392i others(87): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | G | GGGGGGAG others(35): Show |
1 | a0002c0002t0030g0306 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.794-2411_794-2410i others(44): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(5): Show |
G | 4 | a0001c0001t0003g0036 a0001c0001t0039g0183 a0002c0002t0005g0324 others(1): Show |
4 | HG01071.hp1 HG02451.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2188_794-2177d others(14): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(11): Show |
G | 2 | a0001c0001t0061g0056 a0002c0002t0005g0338 |
2 | HG01070.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.794-2194_794-2177d others(20): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(17): Show |
G | 1 | a0002c0002t0014g0315 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.794-2200_794-2177d others(26): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(23): Show |
G | 2 | a0001c0001t0055g0308 a0001c0003t0007g0193 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.794-2206_794-2177d others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(29): Show |
G | 1 | a0001c0005t0007g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.794-2212_794-2177d others(38): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(41): Show |
G | 1 | a0001c0001t0011g0080 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.794-2224_794-2177d others(50): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(53): Show |
G | 1 | a0001c0003t0007g0189 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.794-2236_794-2177d others(62): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(59): Show |
G | 1 | a0002c0002t0063g0294 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.794-2242_794-2177d others(68): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(65): Show |
G | 2 | a0001c0001t0001g0216 a0001c0001t0015g0047 |
2 | HG01981.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.794-2248_794-2177d others(74): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(71): Show |
G | 2 | a0001c0001t0001g0225 a0001c0001t0020g0348 |
2 | HG00733.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.794-2254_794-2177d others(80): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(77): Show |
G | 1 | a0001c0001t0084g0249 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.794-2260_794-2177d others(86): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(95): Show |
G | 2 | a0001c0001t0003g0037 a0001c0003t0121g0178 |
2 | HG03017.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.794-2278_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(113): Show |
G | 1 | a0001c0001t0052g0347 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.794-2296_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(137): Show |
G | 2 | a0001c0001t0002g0247 a0001c0001t0112g0040 |
2 | HG01081.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.794-2320_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(143): Show |
G | 1 | a0001c0001t0027g0200 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.794-2326_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(155): Show |
G | 1 | a0001c0001t0001g0017 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.794-2338_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(161): Show |
G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0205 |
2 | HG02004.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.794-2344_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(167): Show |
G | 1 | a0002c0002t0062g0352 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.794-2350_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(173): Show |
G | 2 | a0001c0001t0077g0051 a0001c0001t0095g0046 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.794-2356_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(179): Show |
G | 3 | a0001c0001t0038g0045 a0001c0001t0038g0169 a0001c0001t0096g0049 |
3 | HG02071.hp1 HG02965.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.794-2362_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579001 | GGGGAGAG others(185): Show |
G | 4 | a0001c0001t0001g0017 a0001c0001t0094g0050 a0001c0001t0097g0256 others(1): Show |
4 | HG02622.hp2 NA18944.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2368_794-2177d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579001 | ||||||
| chr18:49579002 | G | GGGAGACG others(5): Show |
1 | a0001c0001t0128g0060 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.794-2408_794-2407i others(14): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579002 | ||||||
| chr18:49579003 | G | GGAGAGGG others(3): Show |
1 | a0002c0002t0009g0337 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.794-2410_794-2401d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579003 | ||||||
| chr18:49579004 | G | GAGAGGTA others(221): Show |
2 | a0001c0001t0001g0100 a0002c0002t0050g0307 |
2 | NA19083.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.794-2406_794-2405i others(230): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579004 | ||||||
| chr18:49579004 | G | GGGAGAGG others(187): Show |
1 | a0001c0001t0037g0135 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.794-2411_794-2410i others(196): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579004 | |||||||
| chr18:49579007 | A | G | 1 | a0001c0003t0045g0196 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.794-2408A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579007 | |||||||
| chr18:49579007 | AGGGAGAG others(34): Show |
A | 1 | a0001c0001t0032g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.794-2407_794-2367d others(43): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579007 | |||||||
| chr18:49579008 | G | C | 1 | a0001c0001t0128g0060 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.794-2407G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579008 | |||||||
| chr18:49579008 | GGGAGAGG others(106): Show |
G | 1 | a0001c0001t0034g0105 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.794-2404_794-2292d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579008 | ||||||
| chr18:49579008 | GGGAGAGG others(190): Show |
G | 2 | a0001c0001t0104g0160 a0001c0001t0105g0159 |
2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.794-2404_794-2208d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579008 | ||||||
| chr18:49579008 | GGGAGAGG others(196): Show |
G | 3 | a0001c0001t0041g0158 a0001c0001t0110g0161 a0001c0001t0117g0157 |
3 | HG02970.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.794-2404_794-2202d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579008 | ||||||
| chr18:49579009 | G | GAGAGGGA others(30): Show |
1 | a0001c0001t0001g0068 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.794-2406_794-2405i others(39): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579009 | |||||||
| chr18:49579009 | G | GGAGAGGG others(19): Show |
1 | a0001c0001t0018g0140 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.794-2402_794-2377d others(28): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579009 | ||||||
| chr18:49579010 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2405G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579010 | |||||||
| chr18:49579011 | A | C | 1 | a0001c0001t0049g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.794-2404A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579011 | |||||||
| chr18:49579011 | A | G | 2 | a0002c0002t0022g0304 a0002c0002t0030g0292 |
2 | NA18998.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.794-2404A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579011 | |||||||
| chr18:49579013 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2399dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579013 | ||||||
| chr18:49579014 | G | C | 3 | a0001c0001t0128g0060 a0004c0006t0087g0167 a0004c0006t0088g0166 |
3 | HG01346.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.794-2401G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579014 | |||||||
| chr18:49579015 | G | C | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.794-2400G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579015 | |||||||
| chr18:49579015 | G | T | 1 | a0001c0001t0002g0108 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.794-2400G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579015 | |||||||
| chr18:49579016 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2399G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579016 | |||||||
| chr18:49579017 | A | AGAGGGAG others(31): Show |
1 | a0001c0001t0048g0260 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.794-2391_794-2390i others(40): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579017 | ||||||
| chr18:49579017 | A | G | 16 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(13): Show |
16 | HG00738.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.794-2398A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579017 | |||||||
| chr18:49579017 | A | T | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.794-2398A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579017 | |||||||
| chr18:49579018 | GAGGGAGA others(30): Show |
G | 1 | a0004c0006t0088g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.794-2396_794-2360d others(39): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579018 | |||||||
| chr18:49579018 | GAGGGAGA others(36): Show |
G | 1 | a0004c0006t0087g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.794-2396_794-2354d others(45): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579018 | |||||||
| chr18:49579019 | A | AG | 4 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(1): Show |
4 | HG01257.hp1 HG02148.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2393dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579019 | ||||||
| chr18:49579019 | A | G | 1 | a0001c0001t0053g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.794-2396A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579019 | |||||||
| chr18:49579020 | G | C | 1 | a0001c0001t0128g0060 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.794-2395G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579020 | |||||||
| chr18:49579020 | G | GGGAGAGG others(46): Show |
1 | a0001c0001t0003g0104 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.794-2392_794-2340d others(55): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579020 | ||||||
| chr18:49579020 | G | GGGAGAGG others(118): Show |
1 | a0001c0001t0003g0077 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.794-2392_794-2268d others(127): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579020 | ||||||
| chr18:49579021 | GGAGAGGG others(93): Show |
G | 1 | a0001c0001t0001g0237 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.794-2392_794-2293d others(102): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579021 | ||||||
| chr18:49579021 | GGAGAGGG others(163): Show |
G | 1 | a0001c0001t0024g0008 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.794-2390_794-2221d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579021 | ||||||
| chr18:49579021 | GGAGAGGG others(169): Show |
G | 1 | a0001c0001t0076g0065 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.794-2390_794-2215d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579021 | ||||||
| chr18:49579022 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2393G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579022 | |||||||
| chr18:49579023 | A | G | 14 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(11): Show |
14 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.794-2392A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579023 | |||||||
| chr18:49579025 | A | AG | 4 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(1): Show |
4 | HG01257.hp1 HG02148.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2387dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579025 | ||||||
| chr18:49579025 | A | G | 2 | a0001c0001t0003g0033 a0001c0001t0053g0318 |
2 | HG00733.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.794-2390A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579025 | |||||||
| chr18:49579027 | G | A | 1 | a0001c0001t0035g0117 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.794-2388G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579027 | |||||||
| chr18:49579027 | GGAGAGGG others(147): Show |
G | 2 | a0001c0001t0033g0265 a0001c0001t0083g0263 |
2 | HG00738.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.794-2386_794-2233d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579027 | ||||||
| chr18:49579027 | GGAGAGGG others(151): Show |
G | 1 | a0001c0001t0024g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.794-2384_794-2227d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579027 | ||||||
| chr18:49579027 | GGAGAGGG others(153): Show |
G | 2 | a0001c0001t0033g0264 a0001c0001t0086g0262 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.794-2386_794-2227d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579027 | ||||||
| chr18:49579027 | GGAGAGGG others(163): Show |
G | 1 | a0001c0001t0024g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.794-2384_794-2215d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579027 | ||||||
| chr18:49579028 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2387G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579028 | |||||||
| chr18:49579029 | A | G | 14 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(11): Show |
14 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.794-2386A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579029 | |||||||
| chr18:49579031 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2381dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579031 | ||||||
| chr18:49579031 | A | G | 2 | a0001c0001t0003g0033 a0001c0001t0053g0318 |
2 | HG00733.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.794-2384A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579031 | |||||||
| chr18:49579033 | GGAGAGGG others(9): Show |
G | 1 | a0001c0001t0012g0111 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2380_794-2365d others(18): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579033 | ||||||
| chr18:49579034 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2381G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579034 | |||||||
| chr18:49579034 | GAGAGGGA others(170): Show |
G | 1 | a0004c0006t0029g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.794-2380_794-2204d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579034 | |||||||
| chr18:49579035 | A | G | 14 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(11): Show |
14 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.794-2380A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579035 | |||||||
| chr18:49579037 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2375dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579037 | ||||||
| chr18:49579037 | A | G | 1 | a0001c0001t0053g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.794-2378A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579037 | |||||||
| chr18:49579038 | GGGAGAGG others(154): Show |
G | 5 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2374_794-2214d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579038 | ||||||
| chr18:49579040 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2375G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579040 | |||||||
| chr18:49579040 | GAGAGGGA others(152): Show |
G | 1 | a0004c0006t0029g0019 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.794-2374_794-2216d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579040 | |||||||
| chr18:49579041 | A | G | 9 | a0001c0001t0003g0033 a0001c0001t0017g0279 a0003c0004t0016g0144 others(6): Show |
9 | HG00733.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.794-2374A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579041 | |||||||
| chr18:49579043 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2369dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579043 | ||||||
| chr18:49579043 | A | G | 1 | a0001c0001t0053g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.794-2372A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579043 | |||||||
| chr18:49579044 | G | GGGAGAGG others(22): Show |
1 | a0001c0001t0012g0012 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.794-2368_794-2340d others(31): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579044 | ||||||
| chr18:49579044 | GGGAGAGG others(148): Show |
G | 1 | a0001c0001t0017g0279 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.794-2368_794-2214d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579044 | ||||||
| chr18:49579045 | G | A | 1 | a0001c0001t0035g0117 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.794-2370G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579045 | |||||||
| chr18:49579045 | G | GAGAGGGA others(105): Show |
1 | a0005c0009t0013g0125 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.794-2370_794-2369i others(114): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579045 | |||||||
| chr18:49579046 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2369G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579046 | |||||||
| chr18:49579046 | GAGAGGGA others(170): Show |
G | 1 | a0004c0006t0075g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.794-2368_794-2192d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579046 | |||||||
| chr18:49579047 | A | G | 8 | a0001c0001t0003g0033 a0003c0004t0016g0144 a0003c0004t0016g0145 others(5): Show |
8 | HG00733.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.794-2368A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579047 | |||||||
| chr18:49579049 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2363dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579049 | ||||||
| chr18:49579049 | A | AGGGAGAG others(48): Show |
1 | a0002c0002t0073g0345 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.794-2363_794-2309d others(57): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579049 | ||||||
| chr18:49579049 | A | C | 1 | a0001c0001t0032g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.794-2366A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579049 | |||||||
| chr18:49579050 | G | GGGAGAGG others(10): Show |
1 | a0001c0001t0019g0240 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.794-2362_794-2346d others(19): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579050 | ||||||
| chr18:49579050 | GGGAGAGG others(142): Show |
G | 6 | a0003c0004t0016g0144 a0003c0004t0016g0145 a0003c0004t0016g0147 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2362_794-2214d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579050 | ||||||
| chr18:49579052 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2363G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579052 | |||||||
| chr18:49579052 | GAGAGGGA others(128): Show |
G | 1 | a0001c0001t0003g0033 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.794-2362_794-2228d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579052 | |||||||
| chr18:49579053 | A | G | 1 | a0001c0001t0053g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.794-2362A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579053 | |||||||
| chr18:49579055 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2357dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579055 | ||||||
| chr18:49579055 | A | G | 1 | a0001c0001t0012g0111 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2360A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579055 | |||||||
| chr18:49579058 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2357G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579058 | |||||||
| chr18:49579058 | GAGAGGGA others(134): Show |
G | 1 | a0001c0001t0053g0318 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.794-2356_794-2216d others(2): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579058 | |||||||
| chr18:49579061 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2351dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579061 | ||||||
| chr18:49579061 | A | G | 1 | a0001c0001t0012g0111 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2354A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579061 | |||||||
| chr18:49579063 | G | A | 1 | a0001c0001t0035g0117 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.794-2352G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579063 | |||||||
| chr18:49579064 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2351G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579064 | |||||||
| chr18:49579067 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2345dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579067 | ||||||
| chr18:49579067 | A | G | 1 | a0001c0001t0012g0111 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2348A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579067 | |||||||
| chr18:49579070 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2345G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579070 | |||||||
| chr18:49579073 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2339dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579073 | ||||||
| chr18:49579073 | A | G | 1 | a0001c0001t0012g0111 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2342A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579073 | |||||||
| chr18:49579076 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2339G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579076 | |||||||
| chr18:49579079 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2333dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579079 | ||||||
| chr18:49579079 | A | G | 1 | a0001c0001t0012g0111 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2336A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579079 | |||||||
| chr18:49579080 | G | C | 1 | a0002c0002t0063g0294 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.794-2335G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579080 | |||||||
| chr18:49579080 | G | GGAGAGGA others(31): Show |
1 | a0002c0013t0004g0310 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.794-2334_794-2333i others(40): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579080 | ||||||
| chr18:49579081 | G | A | 1 | a0001c0001t0035g0117 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.794-2334G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579081 | |||||||
| chr18:49579082 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2333G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579082 | |||||||
| chr18:49579083 | A | C | 1 | a0001c0001t0015g0047 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.794-2332A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579083 | |||||||
| chr18:49579085 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2327dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579085 | ||||||
| chr18:49579085 | A | G | 1 | a0001c0001t0012g0111 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2330A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579085 | |||||||
| chr18:49579086 | G | C | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2329G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579086 | |||||||
| chr18:49579088 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2327G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579088 | |||||||
| chr18:49579089 | A | C | 2 | a0001c0001t0015g0047 a0002c0002t0063g0294 |
2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2326A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579089 | |||||||
| chr18:49579091 | A | AG | 6 | a0001c0001t0001g0068 a0001c0001t0002g0099 a0001c0001t0002g0118 others(3): Show |
6 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2321dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579091 | ||||||
| chr18:49579091 | A | G | 1 | a0001c0001t0012g0111 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.794-2324A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579091 | |||||||
| chr18:49579092 | G | C | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2323G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579092 | |||||||
| chr18:49579094 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2321G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579094 | |||||||
| chr18:49579095 | A | C | 2 | a0001c0001t0015g0047 a0002c0002t0063g0294 |
2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2320A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579095 | |||||||
| chr18:49579097 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2315dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579097 | ||||||
| chr18:49579097 | A | AGGGAGAG others(33): Show |
1 | a0001c0001t0043g0121 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.794-2310_794-2309i others(42): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579097 | ||||||
| chr18:49579097 | A | G | 2 | a0001c0001t0001g0216 a0001c0001t0012g0111 |
2 | HG01168.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.794-2318A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579097 | |||||||
| chr18:49579098 | G | C | 2 | a0001c0001t0011g0080 a0001c0001t0020g0348 |
2 | HG00733.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.794-2317G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579098 | |||||||
| chr18:49579099 | G | A | 1 | a0001c0001t0035g0117 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.794-2316G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579099 | |||||||
| chr18:49579100 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2315G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579100 | |||||||
| chr18:49579101 | A | AGAGGGAG others(96): Show |
1 | a0002c0002t0071g0333 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.794-2286_794-2285i others(105): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579101 | ||||||
| chr18:49579101 | A | C | 2 | a0001c0001t0015g0047 a0002c0002t0063g0294 |
2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2314A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579101 | |||||||
| chr18:49579101 | A | G | 1 | a0002c0013t0004g0310 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.794-2314A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579101 | |||||||
| chr18:49579103 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01257.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2309dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579103 | ||||||
| chr18:49579103 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0012g0111 |
2 | HG01168.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.794-2312A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579103 | |||||||
| chr18:49579104 | G | C | 2 | a0001c0001t0011g0080 a0001c0001t0020g0348 |
2 | HG00733.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.794-2311G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579104 | |||||||
| chr18:49579106 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2309G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579106 | |||||||
| chr18:49579107 | A | C | 2 | a0001c0001t0015g0047 a0002c0002t0063g0294 |
2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2308A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579107 | |||||||
| chr18:49579109 | A | AG | 4 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(1): Show |
4 | HG01981.hp2 HG02148.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2303dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579109 | ||||||
| chr18:49579109 | A | G | 2 | a0001c0001t0001g0216 a0001c0001t0012g0111 |
2 | HG01168.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.794-2306A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579109 | |||||||
| chr18:49579110 | G | C | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2305G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579110 | |||||||
| chr18:49579112 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2303G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579112 | |||||||
| chr18:49579112 | GAGA | G | 3 | a0001c0001t0035g0117 a0001c0001t0090g0116 a0003c0004t0109g0199 |
3 | HG01257.hp1 HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.794-2302_794-2300d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579112 | |||||||
| chr18:49579113 | A | C | 2 | a0001c0001t0015g0047 a0002c0002t0063g0294 |
2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2302A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579113 | |||||||
| chr18:49579115 | A | AG | 4 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(1): Show |
4 | HG01981.hp2 HG02148.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2297dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579115 | ||||||
| chr18:49579115 | A | G | 3 | a0001c0001t0001g0216 a0001c0001t0001g0225 a0001c0001t0012g0111 |
3 | HG01168.hp1 NA19067.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.794-2300A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579115 | |||||||
| chr18:49579116 | G | GGGAGAGG others(63): Show |
1 | a0001c0001t0001g0269 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.794-2232_794-2231i others(72): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579116 | ||||||
| chr18:49579117 | G | A | 3 | a0001c0001t0035g0117 a0001c0001t0090g0116 a0003c0004t0109g0199 |
3 | HG01257.hp1 HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.794-2298G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579117 | |||||||
| chr18:49579118 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2297G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579118 | |||||||
| chr18:49579119 | A | C | 2 | a0001c0001t0015g0047 a0002c0002t0063g0294 |
2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2296A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579119 | |||||||
| chr18:49579119 | A | G | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2296A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579119 | |||||||
| chr18:49579119 | A | T | 1 | a0001c0001t0084g0249 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.794-2296A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579119 | |||||||
| chr18:49579120 | GA | G | 3 | a0001c0001t0035g0117 a0001c0001t0090g0116 a0003c0004t0109g0199 |
3 | HG01257.hp1 HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.794-2294delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579120 | |||||||
| chr18:49579121 | A | AG | 4 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(1): Show |
4 | HG01981.hp2 HG02148.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2291dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579121 | ||||||
| chr18:49579121 | A | G | 3 | a0001c0001t0001g0216 a0001c0001t0001g0225 a0001c0001t0012g0111 |
3 | HG01168.hp1 NA19067.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.794-2294A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579121 | |||||||
| chr18:49579122 | G | GGGAGAGG others(4): Show |
1 | a0001c0001t0002g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.794-2290_794-2280d others(13): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579122 | ||||||
| chr18:49579124 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2291G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579124 | |||||||
| chr18:49579125 | A | C | 2 | a0001c0001t0015g0047 a0002c0002t0063g0294 |
2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2290A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579125 | |||||||
| chr18:49579125 | A | G | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2290A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579125 | |||||||
| chr18:49579125 | A | T | 1 | a0001c0001t0084g0249 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.794-2290A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579125 | |||||||
| chr18:49579127 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01261.hp2 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2285dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579127 | ||||||
| chr18:49579127 | A | G | 5 | a0001c0001t0001g0216 a0001c0001t0001g0225 a0001c0001t0001g0237 others(2): Show |
5 | HG01168.hp1 HG03017.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2288A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579127 | |||||||
| chr18:49579130 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2285G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579130 | |||||||
| chr18:49579130 | GAGA | G | 3 | a0001c0001t0035g0117 a0001c0001t0090g0116 a0003c0004t0109g0199 |
3 | HG01257.hp1 HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.794-2284_794-2282d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579130 | |||||||
| chr18:49579131 | A | C | 2 | a0001c0001t0015g0047 a0002c0002t0063g0294 |
2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2284A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579131 | |||||||
| chr18:49579131 | A | G | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2284A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579131 | |||||||
| chr18:49579133 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(2): Show |
5 | HG01261.hp2 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2279dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579133 | ||||||
| chr18:49579133 | A | G | 5 | a0001c0001t0001g0216 a0001c0001t0001g0225 a0001c0001t0001g0237 others(2): Show |
5 | HG01168.hp1 HG03017.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2282A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579133 | |||||||
| chr18:49579135 | G | A | 3 | a0001c0001t0035g0117 a0001c0001t0090g0116 a0003c0004t0109g0199 |
3 | HG01257.hp1 HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.794-2280G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579135 | |||||||
| chr18:49579136 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2279G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579136 | |||||||
| chr18:49579137 | A | C | 2 | a0001c0001t0015g0047 a0002c0002t0063g0294 |
2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2278A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579137 | |||||||
| chr18:49579137 | A | G | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2278A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579137 | |||||||
| chr18:49579138 | GA | G | 3 | a0001c0001t0035g0117 a0001c0001t0090g0116 a0003c0004t0109g0199 |
3 | HG01257.hp1 HG02004.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.794-2276delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579138 | |||||||
| chr18:49579139 | A | AG | 6 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(3): Show |
6 | HG01261.hp2 HG01981.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2273dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579139 | ||||||
| chr18:49579139 | A | G | 5 | a0001c0001t0001g0216 a0001c0001t0001g0225 a0001c0001t0001g0237 others(2): Show |
5 | HG01168.hp1 HG03017.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2276A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579139 | |||||||
| chr18:49579142 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2273G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579142 | |||||||
| chr18:49579143 | A | C | 2 | a0001c0001t0015g0047 a0002c0002t0063g0294 |
2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2272A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579143 | |||||||
| chr18:49579143 | A | G | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2272A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579143 | |||||||
| chr18:49579145 | A | AG | 4 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0105 others(1): Show |
4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2267dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579145 | ||||||
| chr18:49579145 | A | G | 4 | a0001c0001t0001g0237 a0001c0001t0003g0037 a0001c0001t0012g0111 others(1): Show |
4 | HG00741.hp1 HG01168.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2270A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579145 | |||||||
| chr18:49579146 | G | GGGAGAGG others(111): Show |
1 | a0001c0001t0001g0242 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.794-2250_794-2249i others(120): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579146 | ||||||
| chr18:49579148 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2267G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579148 | |||||||
| chr18:49579148 | GAGA | G | 4 | a0001c0001t0034g0098 a0001c0001t0035g0117 a0001c0001t0090g0116 others(1): Show |
4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2266_794-2264d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579148 | |||||||
| chr18:49579149 | A | C | 2 | a0001c0001t0015g0047 a0002c0002t0063g0294 |
2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2266A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579149 | |||||||
| chr18:49579149 | A | G | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2266A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579149 | |||||||
| chr18:49579151 | A | AG | 5 | a0001c0001t0001g0068 a0001c0001t0002g0099 a0001c0001t0002g0118 others(2): Show |
5 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2261dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579151 | ||||||
| chr18:49579151 | A | G | 4 | a0001c0001t0001g0237 a0001c0001t0003g0037 a0001c0001t0012g0111 others(1): Show |
4 | HG00741.hp1 HG01168.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2264A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579151 | |||||||
| chr18:49579153 | G | A | 4 | a0001c0001t0034g0098 a0001c0001t0035g0117 a0001c0001t0090g0116 others(1): Show |
4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2262G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579153 | |||||||
| chr18:49579154 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2261G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579154 | |||||||
| chr18:49579155 | A | AGAGGGAG others(99): Show |
1 | a0002c0002t0067g0309 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.794-2177_794-2176i others(108): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579155 | ||||||
| chr18:49579155 | A | C | 2 | a0001c0001t0015g0047 a0002c0002t0063g0294 |
2 | HG01981.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.794-2260A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579155 | |||||||
| chr18:49579155 | A | G | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2260A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579155 | |||||||
| chr18:49579156 | GA | G | 4 | a0001c0001t0034g0098 a0001c0001t0035g0117 a0001c0001t0090g0116 others(1): Show |
4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2258delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579156 | |||||||
| chr18:49579157 | A | AG | 4 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0105 others(1): Show |
4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2255dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579157 | ||||||
| chr18:49579157 | A | G | 4 | a0001c0001t0001g0237 a0001c0001t0003g0037 a0001c0001t0012g0111 others(1): Show |
4 | HG00741.hp1 HG01168.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2258A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579157 | |||||||
| chr18:49579160 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2255G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579160 | |||||||
| chr18:49579161 | A | C | 1 | a0002c0002t0063g0294 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.794-2254A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579161 | |||||||
| chr18:49579161 | A | G | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2254A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579161 | |||||||
| chr18:49579163 | A | AG | 4 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0105 others(1): Show |
4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2249dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579163 | ||||||
| chr18:49579163 | A | G | 4 | a0001c0001t0001g0237 a0001c0001t0003g0037 a0001c0001t0012g0111 others(1): Show |
4 | HG00741.hp1 HG01168.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2252A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579163 | |||||||
| chr18:49579166 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2249G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579166 | |||||||
| chr18:49579166 | GAGA | G | 4 | a0001c0001t0034g0098 a0001c0001t0035g0117 a0001c0001t0090g0116 others(1): Show |
4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2248_794-2246d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579166 | |||||||
| chr18:49579167 | A | C | 1 | a0002c0002t0063g0294 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.794-2248A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579167 | |||||||
| chr18:49579167 | A | G | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2248A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579167 | |||||||
| chr18:49579169 | A | AG | 4 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0105 others(1): Show |
4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2243dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579169 | ||||||
| chr18:49579169 | A | G | 5 | a0001c0001t0001g0237 a0001c0001t0003g0037 a0001c0001t0012g0111 others(2): Show |
5 | HG00741.hp1 HG01081.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-2246A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579169 | |||||||
| chr18:49579171 | G | A | 4 | a0001c0001t0034g0098 a0001c0001t0035g0117 a0001c0001t0090g0116 others(1): Show |
4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2244G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579171 | |||||||
| chr18:49579172 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2243G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579172 | |||||||
| chr18:49579173 | A | C | 1 | a0002c0002t0063g0294 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.794-2242A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579173 | |||||||
| chr18:49579173 | A | G | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2242A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579173 | |||||||
| chr18:49579174 | GA | G | 4 | a0001c0001t0034g0098 a0001c0001t0035g0117 a0001c0001t0090g0116 others(1): Show |
4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2240delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579174 | |||||||
| chr18:49579175 | A | AG | 4 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0105 others(1): Show |
4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2237dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579175 | ||||||
| chr18:49579175 | A | G | 4 | a0001c0001t0001g0237 a0001c0001t0003g0037 a0001c0001t0052g0347 others(1): Show |
4 | HG00741.hp1 HG01081.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2240A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579175 | |||||||
| chr18:49579178 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2237G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579178 | |||||||
| chr18:49579179 | A | C | 1 | a0002c0002t0063g0294 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.794-2236A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579179 | |||||||
| chr18:49579179 | A | G | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2236A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579179 | |||||||
| chr18:49579181 | A | AG | 4 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0105 others(1): Show |
4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2231dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579181 | ||||||
| chr18:49579181 | A | G | 5 | a0001c0001t0001g0237 a0001c0001t0003g0037 a0001c0001t0012g0111 others(2): Show |
5 | HG00741.hp1 HG01081.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-2234A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579181 | |||||||
| chr18:49579184 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2231G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579184 | |||||||
| chr18:49579184 | GAGA | G | 4 | a0001c0001t0034g0098 a0001c0001t0035g0117 a0001c0001t0090g0116 others(1): Show |
4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2230_794-2228d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579184 | |||||||
| chr18:49579185 | A | G | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-2230A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579185 | |||||||
| chr18:49579187 | A | AG | 4 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0105 others(1): Show |
4 | HG01261.hp2 HG01981.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2225dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579187 | ||||||
| chr18:49579187 | A | G | 7 | a0001c0001t0001g0237 a0001c0001t0003g0037 a0001c0001t0012g0111 others(4): Show |
7 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.794-2228A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579187 | |||||||
| chr18:49579188 | G | GGGAGAGG others(34): Show |
1 | a0001c0001t0002g0091 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.794-2224_794-2184d others(43): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579188 | ||||||
| chr18:49579189 | G | A | 4 | a0001c0001t0034g0098 a0001c0001t0035g0117 a0001c0001t0090g0116 others(1): Show |
4 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2226G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579189 | |||||||
| chr18:49579190 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2225G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579190 | |||||||
| chr18:49579191 | A | G | 2 | a0001c0001t0020g0348 a0001c0001t0024g0064 |
2 | HG00733.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.794-2224A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579191 | |||||||
| chr18:49579192 | GA | G | 5 | a0001c0001t0003g0033 a0001c0001t0034g0098 a0001c0001t0035g0117 others(2): Show |
5 | HG00733.hp2 HG01257.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-2222delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579192 | |||||||
| chr18:49579193 | A | AG | 5 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0105 others(2): Show |
5 | HG01243.hp2 HG01261.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2219dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579193 | ||||||
| chr18:49579193 | A | G | 8 | a0001c0001t0001g0237 a0001c0001t0003g0037 a0001c0001t0033g0264 others(5): Show |
8 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.794-2222A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579193 | |||||||
| chr18:49579196 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2219G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579196 | |||||||
| chr18:49579197 | A | G | 5 | a0001c0001t0003g0033 a0001c0001t0020g0348 a0001c0001t0024g0008 others(2): Show |
5 | HG00733.hp1 HG00733.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2218A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579197 | |||||||
| chr18:49579199 | A | G | 8 | a0001c0001t0001g0237 a0001c0001t0003g0037 a0001c0001t0033g0264 others(5): Show |
8 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.794-2216A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579199 | |||||||
| chr18:49579200 | G | C | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-2215G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579200 | |||||||
| chr18:49579200 | G | GGGAGAGG others(45): Show |
1 | a0001c0001t0025g0245 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.794-2202_794-2201i others(54): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579200 | ||||||
| chr18:49579202 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2213G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579202 | |||||||
| chr18:49579202 | GAGA | G | 6 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(3): Show |
6 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2212_794-2210d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579202 | |||||||
| chr18:49579203 | A | G | 9 | a0001c0001t0003g0033 a0001c0001t0020g0348 a0001c0001t0024g0008 others(6): Show |
10 | HG00733.hp1 HG00733.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.794-2212A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579203 | |||||||
| chr18:49579205 | A | AGGGAGAG others(66): Show |
1 | a0001c0001t0002g0252 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.794-2177_794-2176i others(75): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579205 | ||||||
| chr18:49579205 | A | G | 22 | a0001c0001t0001g0237 a0001c0001t0003g0037 a0001c0001t0017g0274 others(19): Show |
22 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.794-2210A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579205 | |||||||
| chr18:49579206 | G | C | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-2209G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579206 | |||||||
| chr18:49579207 | G | A | 6 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(3): Show |
6 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2208G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579207 | |||||||
| chr18:49579207 | G | GGAGGAGG others(28): Show |
1 | a0002c0002t0004g0311 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.794-2205_794-2204i others(37): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579207 | ||||||
| chr18:49579207 | G | GGGAGAGG others(80): Show |
1 | a0001c0001t0035g0120 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.794-2207_794-2206i others(89): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579207 | ||||||
| chr18:49579208 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2207G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579208 | |||||||
| chr18:49579209 | A | G | 10 | a0001c0001t0003g0033 a0001c0001t0020g0348 a0001c0001t0024g0008 others(7): Show |
11 | HG00733.hp1 HG00733.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.794-2206A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579209 | |||||||
| chr18:49579210 | GA | G | 6 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(3): Show |
6 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2204delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579210 | |||||||
| chr18:49579211 | A | G | 11 | a0001c0001t0001g0237 a0001c0001t0003g0037 a0001c0001t0033g0264 others(8): Show |
11 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.794-2204A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579211 | |||||||
| chr18:49579214 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2201G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579214 | |||||||
| chr18:49579215 | A | G | 9 | a0001c0001t0020g0348 a0001c0001t0024g0008 a0001c0001t0024g0064 others(6): Show |
10 | HG00733.hp1 HG02071.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.794-2200A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579215 | |||||||
| chr18:49579217 | A | AG | 7 | a0001c0001t0034g0105 a0001c0001t0035g0120 a0001c0001t0041g0158 others(4): Show |
7 | HG01261.hp2 HG01981.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-2195dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579217 | ||||||
| chr18:49579217 | A | G | 5 | a0001c0001t0003g0037 a0001c0001t0052g0347 a0001c0001t0053g0318 others(2): Show |
6 | HG00741.hp1 HG01081.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-2198A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579217 | |||||||
| chr18:49579218 | G | C | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-2197G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579218 | |||||||
| chr18:49579218 | G | GGGAGAGG others(34): Show |
1 | a0001c0001t0102g0142 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.794-2177_794-2176i others(43): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579218 | ||||||
| chr18:49579220 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2195G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579220 | |||||||
| chr18:49579220 | GAGA | G | 6 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(3): Show |
6 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2194_794-2192d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579220 | |||||||
| chr18:49579221 | A | G | 9 | a0001c0001t0020g0348 a0001c0001t0024g0008 a0001c0001t0024g0064 others(6): Show |
10 | HG00733.hp1 HG02071.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.794-2194A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579221 | |||||||
| chr18:49579223 | A | AG | 8 | a0001c0001t0034g0105 a0001c0001t0035g0120 a0001c0001t0041g0158 others(5): Show |
8 | HG01261.hp2 HG01981.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.794-2189dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579223 | ||||||
| chr18:49579223 | A | G | 6 | a0001c0001t0003g0033 a0001c0001t0003g0037 a0001c0001t0052g0347 others(3): Show |
7 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.794-2192A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579223 | |||||||
| chr18:49579224 | G | C | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-2191G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579224 | |||||||
| chr18:49579224 | G | GGGAGAGG others(86): Show |
1 | a0001c0001t0002g0088 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.794-2177_794-2176i others(95): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579224 | ||||||
| chr18:49579225 | G | A | 6 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(3): Show |
6 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2190G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579225 | |||||||
| chr18:49579226 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2189G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579226 | |||||||
| chr18:49579227 | A | G | 8 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0038g0045 others(5): Show |
9 | HG02071.hp1 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.794-2188A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579227 | |||||||
| chr18:49579228 | G | C | 1 | a0001c0001t0002g0108 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.794-2187G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579228 | |||||||
| chr18:49579228 | GA | G | 6 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0034g0098 others(3): Show |
6 | HG01257.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-2186delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579228 | |||||||
| chr18:49579229 | A | AG | 8 | a0001c0001t0034g0105 a0001c0001t0035g0120 a0001c0001t0041g0158 others(5): Show |
8 | HG01261.hp2 HG01981.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.794-2183dupG | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579229 | ||||||
| chr18:49579229 | A | G | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2186A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579229 | |||||||
| chr18:49579232 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0037g0135 a0002c0002t0050g0307 |
3 | NA19083.hp1 NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.794-2183G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579232 | |||||||
| chr18:49579233 | A | AGAGGGAG others(54): Show |
1 | a0001c0001t0002g0251 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.794-2177_794-2176i others(63): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579233 | ||||||
| chr18:49579233 | A | G | 3 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0076g0065 |
4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2182A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579233 | |||||||
| chr18:49579233 | A | T | 1 | a0001c0001t0084g0249 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.794-2182A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579233 | |||||||
| chr18:49579234 | G | C | 3 | a0001c0001t0015g0044 a0001c0001t0044g0055 a0001c0001t0124g0153 |
3 | HG01192.hp2 HG01891.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.794-2181G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579234 | |||||||
| chr18:49579234 | G | GAGGGAGA others(47): Show |
1 | a0001c0001t0015g0043 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.794-2177_794-2176i others(56): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579234 | ||||||
| chr18:49579234 | G | GAGGGAGA others(119): Show |
1 | a0001c0001t0010g0154 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.794-2177_794-2176i others(128): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579234 | ||||||
| chr18:49579235 | A | AGGGAGAG others(47): Show |
1 | a0001c0011t0068g0351 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.794-2177_794-2176i others(56): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579235 | ||||||
| chr18:49579236 | G | GGGAGAGG others(76): Show |
1 | a0001c0001t0001g0218 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.794-2177_794-2176i others(85): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579236 | ||||||
| chr18:49579239 | C | T | 2 | a0001c0001t0084g0249 a0001c0001t0085g0254 |
2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.794-2176C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579239 | |||||||
| chr18:49579244 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0047g0203 |
2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.794-2171C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579244 | |||||||
| chr18:49579252 | C | T | 1 | a0001c0001t0124g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.794-2163C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579252 | |||||||
| chr18:49579358 | T | C | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-2057T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579358 | |||||||
| chr18:49579425 | T | C | 5 | a0001c0001t0038g0045 a0001c0001t0038g0169 a0001c0001t0094g0050 others(2): Show |
5 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1990T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579425 | |||||||
| chr18:49579711 | A | G | 5 | a0001c0001t0008g0184 a0001c0001t0008g0187 a0001c0001t0008g0191 others(2): Show |
5 | HG01928.hp1 HG01975.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1704A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579711 | |||||||
| chr18:49579743 | T | C | 3 | a0001c0001t0110g0161 a0004c0006t0029g0019 a0004c0006t0075g0255 |
4 | HG02647.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1672T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579743 | |||||||
| chr18:49579743 | T | G | 4 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1672T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579743 | |||||||
| chr18:49579743 | T | TCTTTC | 3 | a0001c0001t0003g0077 a0001c0001t0010g0155 a0004c0010t0010g0246 |
3 | HG03654.hp1 NA19076.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.794-1651_794-1647d others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579743 | ||||||
| chr18:49579743 | T | TCTTTCCT others(3): Show |
8 | a0001c0001t0006g0007 a0001c0001t0006g0030 a0001c0001t0006g0059 others(5): Show |
8 | HG00639.hp2 HG01243.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.794-1656_794-1647d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579743 | ||||||
| chr18:49579743 | T | TCTTTCCT others(8): Show |
6 | a0001c0001t0008g0184 a0001c0001t0008g0187 a0001c0003t0007g0190 others(3): Show |
6 | HG01109.hp2 HG01928.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-1661_794-1647d others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579743 | ||||||
| chr18:49579743 | T | TCTTTCCT others(13): Show |
8 | a0001c0001t0006g0007 a0001c0001t0008g0016 a0001c0001t0008g0188 others(5): Show |
9 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.794-1666_794-1647d others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579743 | ||||||
| chr18:49579744 | C | CCTTTCCT others(6): Show |
3 | a0001c0001t0104g0160 a0001c0001t0105g0159 a0001c0001t0117g0157 |
3 | HG02647.hp1 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.794-1671_794-1670i others(15): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579744 | |||||||
| chr18:49579744 | C | CCTTTCCT others(12): Show |
1 | a0001c0001t0041g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.794-1671_794-1670i others(21): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579744 | |||||||
| chr18:49579749 | C | CT | 5 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1663dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579749 | ||||||
| chr18:49579757 | T | TTC | 5 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1658_794-1657i others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579757 | |||||||
| chr18:49579759 | C | T | 5 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1656C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579759 | |||||||
| chr18:49579759 | CTTTCCTT others(13): Show |
C | 1 | a0001c0001t0044g0229 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.794-1651_794-1632d others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579759 | ||||||
| chr18:49579759 | CTTTCCTT others(18): Show |
C | 1 | a0001c0001t0049g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.794-1651_794-1627d others(27): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579759 | ||||||
| chr18:49579759 | CTTTCCTT others(23): Show |
C | 4 | a0001c0001t0032g0041 a0001c0001t0032g0042 a0001c0001t0097g0256 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-1651_794-1622d others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579759 | ||||||
| chr18:49579764 | C | CTTTCCTT others(128): Show |
1 | a0007c0007t0026g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(137): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(38): Show |
1 | a0001c0005t0007g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.794-1647_794-1646i others(47): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(13): Show |
4 | a0001c0001t0003g0037 a0001c0001t0044g0055 a0001c0003t0045g0196 others(1): Show |
4 | HG01891.hp1 HG02886.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1647_794-1646i others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(18): Show |
6 | a0001c0001t0008g0198 a0001c0001t0112g0040 a0001c0001t0120g0171 others(3): Show |
6 | HG01081.hp2 HG01261.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-1647_794-1646i others(27): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(23): Show |
2 | a0001c0005t0100g0181 a0006c0008t0008g0284 |
2 | HG01358.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(28): Show |
4 | a0001c0001t0053g0318 a0001c0003t0007g0015 a0001c0005t0007g0175 others(1): Show |
5 | HG01884.hp2 HG02922.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1647_794-1646i others(37): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(33): Show |
1 | a0001c0001t0052g0347 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.794-1647_794-1646i others(42): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(38): Show |
1 | a0001c0001t0107g0185 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(47): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(43): Show |
2 | a0001c0001t0119g0283 a0001c0005t0007g0179 |
2 | HG00423.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(52): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(53): Show |
2 | a0001c0001t0003g0033 a0001c0001t0008g0282 |
2 | HG00544.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(62): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(83): Show |
1 | a0001c0001t0003g0039 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.794-1647_794-1646i others(92): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(8): Show |
2 | a0001c0001t0020g0348 a0001c0001t0128g0060 |
2 | HG00733.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(13): Show |
2 | a0001c0001t0003g0061 a0001c0001t0006g0054 |
2 | HG01934.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(18): Show |
2 | a0001c0001t0003g0031 a0001c0001t0003g0038 |
2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(27): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(23): Show |
2 | a0001c0001t0003g0005 a0001c0001t0123g0005 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(28): Show |
2 | a0001c0001t0003g0034 a0001c0001t0115g0063 |
2 | HG02622.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(37): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(33): Show |
1 | a0001c0001t0003g0035 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(42): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(38): Show |
1 | a0001c0001t0003g0032 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(47): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(63): Show |
1 | a0001c0001t0003g0036 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(72): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(3): Show |
2 | a0001c0001t0003g0076 a0001c0001t0025g0133 |
2 | NA19009.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(26): Show |
1 | a0001c0001t0040g0069 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.794-1647_794-1646i others(35): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(8): Show |
1 | a0001c0001t0003g0074 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(13): Show |
2 | a0001c0001t0131g0268 a0003c0004t0016g0144 |
2 | HG00323.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(18): Show |
3 | a0001c0001t0003g0070 a0001c0001t0006g0109 a0001c0001t0125g0075 |
3 | HG02080.hp1 HG02080.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.794-1647_794-1646i others(27): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCCTT others(113): Show |
1 | a0001c0001t0114g0071 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.794-1647_794-1646i others(122): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCT | 25 | a0001c0001t0001g0214 a0001c0001t0001g0228 a0001c0001t0001g0235 others(22): Show |
26 | HG00099.hp1 HG00558.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.794-1598_794-1594d others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCTTT others(3): Show |
20 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0237 others(17): Show |
20 | HG01069.hp1 HG01433.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.794-1603_794-1594d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCTTT others(8): Show |
7 | a0001c0001t0002g0088 a0001c0001t0002g0099 a0001c0001t0002g0118 others(4): Show |
7 | HG02074.hp1 HG02572.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.794-1608_794-1594d others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCTTT others(13): Show |
7 | a0001c0001t0006g0097 a0001c0001t0013g0115 a0001c0001t0013g0132 others(4): Show |
7 | HG00609.hp1 HG01361.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.794-1613_794-1594d others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCTTT others(18): Show |
4 | a0001c0001t0011g0081 a0001c0001t0013g0087 a0001c0001t0013g0107 others(1): Show |
4 | HG00741.hp2 HG01978.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-1618_794-1594d others(27): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCTTT others(23): Show |
1 | a0003c0004t0016g0147 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.794-1623_794-1594d others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | C | CTTTCTTT others(53): Show |
2 | a0001c0001t0056g0285 a0005c0009t0013g0125 |
2 | HG02293.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.794-1594_794-1593i others(62): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | CTTTCT | C | 36 | a0001c0001t0001g0172 a0001c0001t0001g0201 a0001c0001t0001g0204 others(33): Show |
36 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.794-1598_794-1594d others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | CTTTCTTT others(3): Show |
C | 26 | a0001c0001t0001g0208 a0001c0001t0001g0223 a0001c0001t0002g0103 others(23): Show |
27 | HG00738.hp1 HG01074.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.794-1603_794-1594d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | CTTTCTTT others(8): Show |
C | 41 | a0001c0001t0001g0018 a0001c0001t0001g0068 a0001c0001t0001g0206 others(38): Show |
45 | HG00558.hp2 HG00609.hp2 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.794-1608_794-1594d others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | CTTTCTTT others(13): Show |
C | 7 | a0001c0001t0026g0259 a0001c0001t0081g0258 a0001c0001t0082g0261 others(4): Show |
7 | HG01361.hp2 HG01884.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-1613_794-1594d others(22): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | CTTTCTTT others(18): Show |
C | 38 | a0001c0001t0001g0100 a0001c0001t0102g0142 a0001c0001t0106g0143 others(35): Show |
46 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.794-1618_794-1594d others(27): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579764 | CTTTCTTT others(23): Show |
C | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.794-1623_794-1594d others(32): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579764 | ||||||
| chr18:49579767 | T | TTC | 5 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1648_794-1647i others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579767 | |||||||
| chr18:49579768 | CTTTTCTT others(19): Show |
C | 1 | a0002c0002t0009g0331 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.794-1643_794-1618d others(28): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579768 | ||||||
| chr18:49579769 | T | C | 17 | a0001c0001t0001g0267 a0001c0001t0006g0007 a0001c0001t0008g0194 others(14): Show |
19 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.794-1646T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579769 | |||||||
| chr18:49579772 | T | TCCTTTCC others(104): Show |
1 | a0004c0006t0029g0019 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.794-1642_794-1641i others(113): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579772 | ||||||
| chr18:49579774 | T | C | 18 | a0001c0001t0006g0057 a0001c0001t0006g0058 a0001c0001t0010g0149 others(15): Show |
19 | HG00642.hp1 HG00735.hp1 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.794-1641T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579774 | |||||||
| chr18:49579777 | T | C | 2 | a0001c0001t0105g0159 a0001c0001t0117g0157 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.794-1638T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579777 | |||||||
| chr18:49579777 | T | TCCTTTCC others(69): Show |
1 | a0004c0006t0029g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.794-1637_794-1636i others(78): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579777 | ||||||
| chr18:49579777 | T | TCCTTTCC others(79): Show |
1 | a0004c0006t0075g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.794-1637_794-1636i others(88): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579777 | ||||||
| chr18:49579777 | T | TTCCTTTT others(26): Show |
1 | a0001c0001t0110g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1638_794-1637i others(35): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579777 | |||||||
| chr18:49579778 | C | A | 1 | a0001c0001t0001g0213 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.794-1637C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579778 | |||||||
| chr18:49579779 | T | C | 5 | a0001c0001t0010g0150 a0001c0001t0010g0154 a0001c0001t0010g0162 others(2): Show |
5 | HG03017.hp2 HG03139.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1636T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579779 | |||||||
| chr18:49579781 | TTCTTTTC others(5): Show |
T | 1 | a0002c0002t0004g0311 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.794-1632_794-1621d others(14): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579781 | ||||||
| chr18:49579782 | T | C | 3 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0110g0161 |
3 | HG02647.hp1 HG02970.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.794-1633T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579782 | |||||||
| chr18:49579784 | T | C | 4 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0076g0065 others(1): Show |
5 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1631T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579784 | |||||||
| chr18:49579787 | T | C | 2 | a0001c0001t0110g0161 a0001c0001t0117g0157 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.794-1628T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579787 | |||||||
| chr18:49579789 | T | C | 3 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 |
3 | HG02647.hp1 HG02896.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.794-1626T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579789 | |||||||
| chr18:49579792 | T | C | 1 | a0001c0001t0110g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1623T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579792 | |||||||
| chr18:49579794 | T | C | 5 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1621T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579794 | |||||||
| chr18:49579797 | T | C | 1 | a0001c0001t0110g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1618T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579797 | |||||||
| chr18:49579799 | T | C | 4 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1616T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579799 | |||||||
| chr18:49579802 | T | C | 1 | a0001c0001t0110g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1613T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579802 | |||||||
| chr18:49579804 | T | C | 4 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1611T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579804 | |||||||
| chr18:49579807 | T | C | 1 | a0001c0001t0110g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1608T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579807 | |||||||
| chr18:49579809 | T | C | 4 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1606T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579809 | |||||||
| chr18:49579812 | T | C | 1 | a0001c0001t0110g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1603T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579812 | |||||||
| chr18:49579814 | T | C | 4 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1601T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579814 | |||||||
| chr18:49579817 | T | A | 5 | a0001c0001t0017g0274 a0001c0001t0024g0008 a0001c0001t0024g0064 others(2): Show |
6 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-1598T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579817 | |||||||
| chr18:49579817 | T | C | 1 | a0001c0001t0110g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1598T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579817 | |||||||
| chr18:49579817 | T | TCTTTACT others(3): Show |
1 | a0007c0007t0026g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.794-1593_794-1584d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579817 | ||||||
| chr18:49579817 | T | TCTTTTCT others(3): Show |
1 | a0001c0001t0003g0253 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.794-1594_794-1593i others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579817 | ||||||
| chr18:49579817 | T | TCTTTTCT others(8): Show |
4 | a0001c0001t0017g0276 a0001c0001t0017g0277 a0001c0001t0017g0279 others(1): Show |
4 | HG02572.hp2 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1594_794-1593i others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49579817 | ||||||
| chr18:49579819 | T | C | 4 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1596T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579819 | |||||||
| chr18:49579821 | TAC | T | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-1593_794-1592d others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579821 | |||||||
| chr18:49579822 | A | C | 1 | a0001c0001t0110g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.794-1593A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579822 | |||||||
| chr18:49579822 | A | T | 4 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1593A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579822 | |||||||
| chr18:49579824 | T | C | 4 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1591T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579824 | |||||||
| chr18:49579825 | T | C | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-1590T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579825 | |||||||
| chr18:49579827 | A | T | 4 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1588A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579827 | |||||||
| chr18:49579853 | C | T | 2 | a0001c0001t0032g0041 a0001c0001t0032g0042 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.794-1562C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579853 | |||||||
| chr18:49579880 | C | T | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.794-1535C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579880 | |||||||
| chr18:49579890 | C | T | 1 | a0002c0002t0004g0343 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.794-1525C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579890 | |||||||
| chr18:49579896 | C | T | 5 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1519C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579896 | |||||||
| chr18:49579932 | C | G | 1 | a0001c0001t0033g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.794-1483C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49579932 | |||||||
| chr18:49580040 | C | T | 1 | a0001c0001t0006g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.794-1375C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580040 | |||||||
| chr18:49580187 | A | G | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-1228A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580187 | |||||||
| chr18:49580230 | A | C | 1 | a0006c0008t0008g0284 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.794-1185A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580230 | |||||||
| chr18:49580235 | T | G | 1 | a0006c0008t0008g0284 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.794-1180T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580235 | |||||||
| chr18:49580239 | ACCAACTG others(8): Show |
A | 1 | a0006c0008t0008g0284 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.794-1175_794-1161d others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580239 | |||||||
| chr18:49580255 | A | T | 1 | a0006c0008t0008g0284 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.794-1160A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580255 | |||||||
| chr18:49580257 | C | T | 1 | a0001c0001t0134g0209 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.794-1158C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580257 | |||||||
| chr18:49580385 | C | T | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.794-1030C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580385 | |||||||
| chr18:49580444 | A | G | 12 | a0001c0001t0055g0308 a0001c0001t0107g0185 a0001c0003t0007g0015 others(9): Show |
13 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.794-971A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580444 | |||||||
| chr18:49580567 | C | T | 4 | a0001c0001t0026g0259 a0001c0001t0048g0260 a0001c0001t0081g0258 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-848C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580567 | |||||||
| chr18:49580570 | G | A | 6 | a0001c0001t0010g0148 a0001c0001t0010g0149 a0001c0001t0010g0151 others(3): Show |
6 | HG00639.hp2 HG00735.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-845G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580570 | |||||||
| chr18:49580653 | G | A | 2 | a0002c0002t0004g0290 a0002c0002t0004g0303 |
2 | NA19005.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.794-762G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580653 | |||||||
| chr18:49580658 | GAAAA | G | 5 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-750_794-747del others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr18 | 49580658 | ||||||
| chr18:49580772 | G | C | 1 | a0001c0001t0013g0115 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.794-643G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580772 | |||||||
| chr18:49580782 | C | G | 85 | a0001c0001t0018g0085 a0001c0001t0018g0131 a0001c0001t0018g0140 others(82): Show |
95 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.794-633C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580782 | |||||||
| chr18:49580863 | C | T | 40 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(37): Show |
42 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.794-552C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580863 | |||||||
| chr18:49580918 | T | C | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.794-497T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580918 | |||||||
| chr18:49580980 | C | T | 4 | a0004c0006t0029g0019 a0004c0006t0075g0255 a0004c0006t0087g0167 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-435C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580980 | |||||||
| chr18:49580981 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.794-434G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49580981 | |||||||
| chr18:49581081 | A | G | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.794-334A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49581081 | |||||||
| chr18:49581084 | C | A | 5 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-331C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49581084 | |||||||
| chr18:49581284 | A | G | 12 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.794-131A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49581284 | |||||||
| chr18:49581399 | T | C | 3 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0036g0250 |
3 | NA18975.hp1 NA18982.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.794-16T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 5/9 | chr18 | 49581399 | |||||||
| chr18:49581736 | C | T | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1036+79C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49581736 | |||||||
| chr18:49581737 | A | G | 9 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(6): Show |
10 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+80A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49581737 | |||||||
| chr18:49581806 | T | C | 1 | a0001c0005t0007g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1036+149T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49581806 | |||||||
| chr18:49582081 | C | G | 2 | a0002c0002t0005g0320 a0002c0002t0005g0340 |
2 | HG01256.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1037-281C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49582081 | |||||||
| chr18:49582081 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1037-281C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49582081 | |||||||
| chr18:49582104 | T | A | 1 | a0004c0006t0088g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1037-258T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49582104 | |||||||
| chr18:49582236 | G | A | 18 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(15): Show |
18 | HG00738.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1037-126G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49582236 | |||||||
| chr18:49582286 | T | G | 4 | a0001c0001t0008g0016 a0001c0001t0008g0188 a0001c0001t0008g0198 others(1): Show |
5 | HG01069.hp2 HG01071.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-76T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 6/9 | chr18 | 49582286 | |||||||
| chr18:49582545 | A | G | 2 | a0001c0001t0032g0041 a0001c0001t0032g0042 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1157+63A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582545 | |||||||
| chr18:49582549 | C | A | 1 | a0001c0001t0001g0217 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1157+67C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582549 | |||||||
| chr18:49582558 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0217 |
2 | HG02004.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1157+76G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582558 | |||||||
| chr18:49582558 | G | T | 1 | a0001c0001t0033g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1157+76G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582558 | |||||||
| chr18:49582559 | T | A | 1 | a0001c0001t0033g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1157+77T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582559 | |||||||
| chr18:49582576 | C | T | 1 | a0002c0002t0072g0336 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1157+94C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582576 | |||||||
| chr18:49582584 | A | G | 4 | a0001c0001t0026g0259 a0001c0001t0048g0260 a0001c0001t0081g0258 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1157+102A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582584 | |||||||
| chr18:49582648 | A | G | 15 | a0001c0001t0032g0041 a0001c0001t0032g0042 a0001c0001t0039g0177 others(12): Show |
16 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1157+166A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582648 | |||||||
| chr18:49582710 | C | T | 2 | a0001c0001t0027g0231 a0002c0002t0067g0309 |
2 | NA18948.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1157+228C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582710 | |||||||
| chr18:49582750 | T | G | 3 | a0002c0002t0005g0023 a0002c0002t0028g0327 a0002c0002t0051g0023 |
3 | HG00642.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1157+268T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582750 | |||||||
| chr18:49582773 | T | C | 4 | a0004c0006t0029g0019 a0004c0006t0075g0255 a0004c0006t0087g0167 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+291T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582773 | |||||||
| chr18:49582819 | C | T | 1 | a0001c0001t0020g0348 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1157+337C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582819 | |||||||
| chr18:49582835 | C | T | 11 | a0001c0001t0039g0177 a0001c0001t0039g0183 a0001c0001t0041g0158 others(8): Show |
12 | HG02258.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1157+353C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582835 | |||||||
| chr18:49582875 | GTA | G | 5 | a0001c0001t0038g0045 a0001c0001t0038g0169 a0001c0001t0094g0050 others(2): Show |
5 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+397_1157+398d others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | 49582875 | ||||||
| chr18:49582983 | C | T | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1157+501C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49582983 | |||||||
| chr18:49583005 | G | A | 2 | a0001c0001t0032g0041 a0001c0001t0032g0042 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1157+523G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583005 | |||||||
| chr18:49583007 | A | G | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1157+525A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583007 | |||||||
| chr18:49583009 | G | A | 11 | a0001c0001t0039g0177 a0001c0001t0039g0183 a0001c0001t0041g0158 others(8): Show |
12 | HG02258.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1157+527G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583009 | |||||||
| chr18:49583072 | G | A | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1158-484G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583072 | |||||||
| chr18:49583132 | G | C | 5 | a0001c0001t0032g0041 a0001c0001t0032g0042 a0001c0001t0097g0256 others(2): Show |
5 | HG01891.hp2 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1158-424G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583132 | |||||||
| chr18:49583281 | C | T | 1 | a0001c0001t0012g0111 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1158-275C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583281 | |||||||
| chr18:49583282 | A | C | 1 | a0001c0001t0012g0111 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1158-274A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583282 | |||||||
| chr18:49583283 | G | A | 1 | a0001c0001t0012g0111 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1158-273G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583283 | |||||||
| chr18:49583323 | G | A | 148 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(145): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1158-233G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583323 | |||||||
| chr18:49583397 | G | C | 4 | a0001c0001t0033g0264 a0001c0001t0033g0265 a0001c0001t0083g0263 others(1): Show |
4 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1158-159G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583397 | |||||||
| chr18:49583410 | G | A | 5 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158-146G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583410 | |||||||
| chr18:49583444 | C | T | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1158-112C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583444 | |||||||
| chr18:49583454 | C | T | 6 | a0003c0004t0016g0144 a0003c0004t0016g0145 a0003c0004t0016g0147 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158-102C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583454 | |||||||
| chr18:49583455 | T | C | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1158-101T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583455 | |||||||
| chr18:49583514 | C | T | 1 | a0002c0002t0023g0299 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1158-42C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583514 | |||||||
| chr18:49583552 | G | C | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | splice_region_variant&intron_variant | LOW | c.1158-4G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 7/9 | chr18 | 49583552 | |||||||
| chr18:49583894 | A | T | 13 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0026g0259 others(10): Show |
14 | HG01243.hp2 HG01884.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1376+120A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49583894 | |||||||
| chr18:49584057 | A | T | 1 | a0001c0001t0033g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1376+283A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584057 | |||||||
| chr18:49584090 | G | A | 1 | a0002c0002t0005g0339 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1376+316G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584090 | |||||||
| chr18:49584171 | A | G | 1 | a0001c0001t0012g0141 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1376+397A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584171 | |||||||
| chr18:49584195 | T | A | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1376+421T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584195 | |||||||
| chr18:49584264 | C | T | 2 | a0001c0001t0003g0070 a0001c0001t0040g0069 |
2 | HG02040.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1376+490C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584264 | |||||||
| chr18:49584302 | A | G | 3 | a0001c0001t0032g0041 a0001c0001t0032g0042 a0001c0001t0049g0281 |
3 | HG01891.hp2 HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1376+528A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584302 | |||||||
| chr18:49584412 | G | A | 1 | a0001c0001t0126g0079 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1376+638G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584412 | |||||||
| chr18:49584549 | G | A | 6 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1376+775G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584549 | |||||||
| chr18:49584596 | A | C | 12 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1376+822A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584596 | |||||||
| chr18:49584890 | T | C | 63 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(60): Show |
67 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1376+1116T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49584890 | |||||||
| chr18:49585012 | A | G | 1 | a0001c0001t0114g0071 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1376+1238A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585012 | |||||||
| chr18:49585018 | A | T | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1376+1244A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585018 | |||||||
| chr18:49585121 | G | A | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1376+1347G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585121 | |||||||
| chr18:49585147 | C | T | 1 | a0002c0002t0066g0291 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1376+1373C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585147 | |||||||
| chr18:49585192 | A | G | 268 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(265): Show |
288 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1376+1418A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585192 | |||||||
| chr18:49585259 | C | T | 4 | a0001c0001t0026g0259 a0001c0001t0048g0260 a0001c0001t0081g0258 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1376+1485C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585259 | |||||||
| chr18:49585357 | C | T | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1377-1389C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585357 | |||||||
| chr18:49585362 | C | T | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1377-1384C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585362 | |||||||
| chr18:49585667 | C | A | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1377-1079C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585667 | |||||||
| chr18:49585870 | C | A | 1 | a0002c0002t0130g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1377-876C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585870 | |||||||
| chr18:49585939 | T | C | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1377-807T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585939 | |||||||
| chr18:49585941 | G | C | 7 | a0001c0001t0039g0177 a0001c0001t0039g0183 a0001c0001t0041g0158 others(4): Show |
7 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1377-805G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585941 | |||||||
| chr18:49585942 | G | T | 7 | a0001c0001t0039g0177 a0001c0001t0039g0183 a0001c0001t0041g0158 others(4): Show |
7 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1377-804G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585942 | |||||||
| chr18:49585973 | G | C | 2 | a0001c0001t0084g0249 a0001c0001t0085g0254 |
2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1377-773G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49585973 | |||||||
| chr18:49586082 | C | T | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1377-664C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586082 | |||||||
| chr18:49586199 | T | A | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1377-547T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586199 | |||||||
| chr18:49586233 | G | T | 6 | a0001c0001t0033g0264 a0001c0001t0033g0265 a0001c0001t0083g0263 others(3): Show |
6 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1377-513G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586233 | |||||||
| chr18:49586250 | C | T | 2 | a0001c0001t0102g0142 a0001c0001t0106g0143 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1377-496C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586250 | |||||||
| chr18:49586251 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0001g0273 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1377-495G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586251 | |||||||
| chr18:49586311 | T | C | 268 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(265): Show |
288 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1377-435T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586311 | |||||||
| chr18:49586361 | CACTAACA others(6): Show |
C | 1 | a0001c0001t0137g0092 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1377-383_1377-371d others(15): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr18 | 49586361 | ||||||
| chr18:49586367 | C | G | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1377-379C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586367 | |||||||
| chr18:49586407 | T | A | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1377-339T>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586407 | |||||||
| chr18:49586481 | G | GCCAT | 119 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(116): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1377-265_1377-264i others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586481 | |||||||
| chr18:49586501 | T | C | 38 | a0001c0001t0018g0085 a0001c0001t0018g0131 a0001c0001t0018g0140 others(35): Show |
40 | HG00558.hp2 HG00609.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.1377-245T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586501 | |||||||
| chr18:49586574 | G | T | 24 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0072 others(21): Show |
26 | HG00544.hp1 HG02056.hp1 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1377-172G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586574 | |||||||
| chr18:49586626 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1377-120G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586626 | |||||||
| chr18:49586638 | C | T | 119 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(116): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1377-108C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586638 | |||||||
| chr18:49586642 | A | C | 1 | a0001c0001t0001g0235 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1377-104A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 8/9 | chr18 | 49586642 | |||||||
| chr18:49586942 | A | G | 7 | a0001c0001t0039g0177 a0001c0001t0039g0183 a0001c0001t0041g0158 others(4): Show |
7 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1481+92A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49586942 | |||||||
| chr18:49586994 | C | T | 1 | a0001c0001t0018g0140 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1481+144C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49586994 | |||||||
| chr18:49587001 | G | C | 2 | a0001c0001t0038g0045 a0001c0001t0038g0169 |
2 | HG02071.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1481+151G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587001 | |||||||
| chr18:49587106 | T | TA | 26 | a0001c0001t0002g0251 a0001c0001t0017g0274 a0001c0001t0017g0276 others(23): Show |
26 | HG00738.hp1 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1481+273dupA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587106 | ||||||
| chr18:49587106 | TA | T | 139 | a0001c0001t0001g0215 a0001c0001t0003g0005 a0001c0001t0003g0031 others(136): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1481+273delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587106 | ||||||
| chr18:49587274 | CAAAA | C | 6 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0113 others(3): Show |
6 | HG00738.hp2 HG01099.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1481+426_1481+429d others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587274 | ||||||
| chr18:49587285 | A | G | 1 | a0001c0001t0098g0257 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1481+435A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587285 | |||||||
| chr18:49587356 | G | C | 50 | a0001c0001t0018g0085 a0001c0001t0018g0131 a0001c0001t0018g0140 others(47): Show |
53 | HG00558.hp2 HG00609.hp2 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.1481+506G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587356 | |||||||
| chr18:49587437 | C | T | 4 | a0001c0001t0015g0006 a0001c0001t0015g0047 a0001c0001t0015g0048 others(1): Show |
5 | HG00642.hp1 HG01074.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1481+587C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587437 | |||||||
| chr18:49587508 | G | A | 3 | a0001c0001t0048g0260 a0001c0001t0081g0258 a0001c0001t0082g0261 |
3 | HG01243.hp2 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1481+658G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587508 | |||||||
| chr18:49587510 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1481+660A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587510 | |||||||
| chr18:49587527 | C | T | 11 | a0001c0001t0032g0041 a0001c0001t0032g0042 a0001c0001t0033g0264 others(8): Show |
12 | HG00738.hp1 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1481+677C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587527 | |||||||
| chr18:49587563 | C | T | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1481+713C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587563 | |||||||
| chr18:49587568 | C | CA | 128 | a0001c0001t0001g0017 a0001c0001t0001g0100 a0001c0001t0001g0202 others(125): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1481+744dupA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | ||||||
| chr18:49587568 | C | CAA | 36 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0003g0039 others(33): Show |
37 | HG00423.hp2 HG00639.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1481+743_1481+744d others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | ||||||
| chr18:49587568 | C | CAAA | 7 | a0001c0001t0032g0041 a0001c0001t0098g0257 a0001c0001t0141g0241 others(4): Show |
9 | HG01167.hp1 HG01346.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1481+742_1481+744d others(5): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | ||||||
| chr18:49587568 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0024g0008 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1481+735_1481+744d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | ||||||
| chr18:49587568 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0024g0064 a0001c0001t0076g0065 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1481+734_1481+744d others(13): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | ||||||
| chr18:49587568 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0082g0261 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1481+730_1481+744d others(17): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | ||||||
| chr18:49587568 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0048g0260 a0001c0001t0081g0258 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1481+729_1481+744d others(18): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | ||||||
| chr18:49587568 | CA | C | 6 | a0001c0001t0002g0091 a0001c0001t0040g0119 a0001c0001t0041g0158 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1481+744delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | ||||||
| chr18:49587568 | CAAAAAAA | C | 7 | a0001c0001t0038g0045 a0001c0001t0038g0169 a0001c0001t0039g0177 others(4): Show |
7 | HG02071.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1481+738_1481+744d others(9): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587568 | ||||||
| chr18:49587684 | C | T | 3 | a0001c0001t0033g0264 a0001c0001t0033g0265 a0001c0001t0083g0263 |
3 | HG00738.hp1 HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1481+834C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587684 | |||||||
| chr18:49587789 | C | CT | 124 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0032 others(121): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1481+950dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49587789 | ||||||
| chr18:49587841 | G | A | 5 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1481+991G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49587841 | |||||||
| chr18:49588113 | TCTC | T | 5 | a0001c0001t0041g0158 a0001c0001t0104g0160 a0001c0001t0105g0159 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1481+1264_1481+126 others(7): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588113 | |||||||
| chr18:49588140 | C | G | 18 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(15): Show |
19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1481+1290C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588140 | |||||||
| chr18:49588199 | G | A | 18 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(15): Show |
19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1481+1349G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588199 | |||||||
| chr18:49588256 | A | G | 28 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(25): Show |
29 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1481+1406A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588256 | |||||||
| chr18:49588265 | C | T | 5 | a0001c0001t0038g0045 a0001c0001t0038g0169 a0001c0001t0094g0050 others(2): Show |
5 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1481+1415C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588265 | |||||||
| chr18:49588282 | C | CT | 103 | a0001c0001t0001g0068 a0001c0001t0001g0267 a0001c0001t0001g0269 others(100): Show |
107 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1481+1450dupT | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49588282 | ||||||
| chr18:49588282 | C | CTT | 13 | a0001c0001t0002g0123 a0001c0001t0002g0134 a0001c0001t0041g0158 others(10): Show |
13 | HG01243.hp2 HG02015.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1481+1449_1481+145 others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49588282 | ||||||
| chr18:49588282 | CTT | C | 14 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(11): Show |
15 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1481+1449_1481+145 others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49588282 | ||||||
| chr18:49588310 | T | C | 18 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(15): Show |
19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1481+1460T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588310 | |||||||
| chr18:49588313 | C | T | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1481+1463C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588313 | |||||||
| chr18:49588314 | A | G | 78 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(75): Show |
82 | HG00558.hp2 HG00609.hp2 HG01243.hp2 others(79): Show |
intron_variant | MODIFIER | c.1481+1464A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588314 | |||||||
| chr18:49588322 | G | A | 3 | a0001c0001t0008g0184 a0001c0001t0008g0187 a0001c0001t0008g0194 |
3 | HG01928.hp1 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1481+1472G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588322 | |||||||
| chr18:49588329 | C | T | 2 | a0004c0006t0087g0167 a0004c0006t0088g0166 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1481+1479C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588329 | |||||||
| chr18:49588375 | C | T | 191 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(188): Show |
201 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1481+1525C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588375 | |||||||
| chr18:49588400 | A | G | 38 | a0001c0001t0018g0085 a0001c0001t0018g0131 a0001c0001t0018g0140 others(35): Show |
40 | HG00558.hp2 HG00609.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.1481+1550A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588400 | |||||||
| chr18:49588401 | A | C | 1 | a0001c0001t0003g0082 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1481+1551A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588401 | |||||||
| chr18:49588402 | C | CTCCTCCA others(12): Show |
1 | a0001c0001t0003g0082 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1481+1552_1481+155 others(23): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588402 | |||||||
| chr18:49588404 | T | C | 1 | a0001c0001t0003g0082 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1481+1554T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588404 | |||||||
| chr18:49588405 | T | C | 1 | a0001c0001t0003g0082 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1481+1555T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588405 | |||||||
| chr18:49588437 | C | T | 18 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(15): Show |
19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1481+1587C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588437 | |||||||
| chr18:49588439 | C | T | 4 | a0001c0001t0006g0097 a0001c0001t0006g0109 a0001c0001t0084g0249 others(1): Show |
4 | HG02040.hp2 HG02080.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481+1589C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588439 | |||||||
| chr18:49588480 | GCCATGTT others(10): Show |
G | 2 | a0001c0001t0039g0177 a0001c0001t0039g0183 |
2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1481+1647_1481+166 others(21): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49588480 | ||||||
| chr18:49588582 | G | C | 20 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(17): Show |
21 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1481+1732G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588582 | |||||||
| chr18:49588588 | C | T | 12 | a0001c0001t0055g0308 a0001c0001t0107g0185 a0001c0003t0007g0015 others(9): Show |
13 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1481+1738C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588588 | |||||||
| chr18:49588589 | G | A | 1 | a0001c0001t0142g0156 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1481+1739G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588589 | |||||||
| chr18:49588603 | A | G | 1 | a0001c0001t0141g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1481+1753A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588603 | |||||||
| chr18:49588635 | A | T | 12 | a0001c0001t0024g0008 a0001c0001t0024g0064 a0001c0001t0041g0158 others(9): Show |
13 | HG01243.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1481+1785A>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588635 | |||||||
| chr18:49588684 | C | T | 8 | a0001c0001t0038g0045 a0001c0001t0038g0169 a0001c0001t0039g0177 others(5): Show |
8 | HG02071.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1482-1817C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588684 | |||||||
| chr18:49588705 | G | A | 2 | a0001c0001t0037g0135 a0002c0002t0005g0339 |
2 | HG01099.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1482-1796G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588705 | |||||||
| chr18:49588775 | C | T | 1 | a0001c0001t0096g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1482-1726C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588775 | |||||||
| chr18:49588800 | A | G | 30 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(27): Show |
31 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.1482-1701A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588800 | |||||||
| chr18:49588833 | C | G | 2 | a0001c0001t0039g0177 a0001c0001t0039g0183 |
2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1482-1668C>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588833 | |||||||
| chr18:49588856 | A | C | 18 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(15): Show |
19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1482-1645A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588856 | |||||||
| chr18:49588869 | A | G | 12 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1482-1632A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588869 | |||||||
| chr18:49588951 | C | T | 18 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(15): Show |
19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1482-1550C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588951 | |||||||
| chr18:49588958 | G | A | 6 | a0001c0001t0033g0264 a0001c0001t0033g0265 a0001c0001t0083g0263 others(3): Show |
6 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1482-1543G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588958 | |||||||
| chr18:49588972 | G | T | 18 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(15): Show |
19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1482-1529G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588972 | |||||||
| chr18:49588994 | C | T | 2 | a0004c0006t0029g0019 a0004c0006t0075g0255 |
3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1482-1507C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49588994 | |||||||
| chr18:49589185 | A | C | 20 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(17): Show |
21 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1482-1316A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589185 | |||||||
| chr18:49589265 | C | T | 2 | a0001c0001t0032g0041 a0001c0001t0032g0042 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1482-1236C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589265 | |||||||
| chr18:49589303 | A | G | 20 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(17): Show |
21 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1482-1198A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589303 | |||||||
| chr18:49589369 | T | G | 6 | a0001c0001t0033g0264 a0001c0001t0033g0265 a0001c0001t0083g0263 others(3): Show |
6 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1482-1132T>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589369 | |||||||
| chr18:49589547 | G | T | 1 | a0001c0001t0015g0048 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1482-954G>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589547 | |||||||
| chr18:49589597 | G | A | 1 | a0001c0001t0015g0048 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1482-904G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589597 | |||||||
| chr18:49589683 | A | G | 28 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(25): Show |
29 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1482-818A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589683 | |||||||
| chr18:49589729 | G | A | 2 | a0001c0001t0039g0177 a0001c0001t0039g0183 |
2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1482-772G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589729 | |||||||
| chr18:49589834 | T | C | 28 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(25): Show |
29 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1482-667T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589834 | |||||||
| chr18:49589954 | G | C | 18 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(15): Show |
19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1482-547G>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49589954 | |||||||
| chr18:49590042 | C | T | 18 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(15): Show |
19 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1482-459C>T | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590042 | |||||||
| chr18:49590060 | T | C | 20 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(17): Show |
21 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1482-441T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590060 | |||||||
| chr18:49590080 | C | A | 6 | a0001c0001t0032g0041 a0001c0001t0032g0042 a0001c0001t0049g0281 others(3): Show |
7 | HG01891.hp2 HG02055.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1482-421C>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590080 | |||||||
| chr18:49590169 | A | G | 2 | a0001c0001t0097g0256 a0001c0001t0098g0257 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1482-332A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590169 | |||||||
| chr18:49590173 | T | TTG | 43 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(40): Show |
45 | HG00423.hp1 HG00544.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1482-294_1482-293d others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | ||||||
| chr18:49590173 | T | TTGTG | 68 | a0001c0001t0001g0100 a0001c0001t0001g0202 a0001c0001t0002g0002 others(65): Show |
73 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1482-296_1482-293d others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | ||||||
| chr18:49590173 | T | TTGTGTG | 52 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0068 others(49): Show |
55 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1482-298_1482-293d others(8): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | ||||||
| chr18:49590173 | T | TTGTGTGT others(1): Show |
9 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0001g0223 others(6): Show |
9 | HG01106.hp1 HG01496.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1482-300_1482-293d others(10): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | ||||||
| chr18:49590173 | TTG | T | 28 | a0001c0001t0006g0097 a0001c0001t0011g0009 a0001c0001t0011g0027 others(25): Show |
32 | HG00609.hp2 HG00741.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1482-294_1482-293d others(4): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | ||||||
| chr18:49590173 | TTGTG | T | 20 | a0001c0001t0010g0149 a0001c0001t0024g0008 a0001c0001t0024g0064 others(17): Show |
22 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(19): Show |
intron_variant | MODIFIER | c.1482-296_1482-293d others(6): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | ||||||
| chr18:49590173 | TTGTGTG | T | 17 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(14): Show |
17 | HG00735.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1482-298_1482-293d others(8): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | ||||||
| chr18:49590173 | TTGTGTGT others(1): Show |
T | 15 | a0001c0001t0038g0045 a0001c0001t0038g0169 a0001c0001t0094g0050 others(12): Show |
15 | HG02055.hp2 HG02071.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1482-300_1482-293d others(10): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | ||||||
| chr18:49590173 | TTGTGTGT others(3): Show |
T | 4 | a0001c0001t0039g0177 a0001c0001t0039g0183 a0001c0001t0042g0014 others(1): Show |
5 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1482-302_1482-293d others(12): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | ||||||
| chr18:49590173 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0010g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1482-304_1482-293d others(14): Show |
LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | 49590173 | ||||||
| chr18:49590220 | G | A | 1 | a0002c0002t0021g0349 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1482-281G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590220 | |||||||
| chr18:49590231 | A | C | 4 | a0001c0001t0033g0264 a0001c0001t0033g0265 a0001c0001t0083g0263 others(1): Show |
4 | HG00738.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482-270A>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590231 | |||||||
| chr18:49590305 | A | G | 68 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(65): Show |
71 | HG00558.hp2 HG00609.hp2 HG01243.hp2 others(68): Show |
intron_variant | MODIFIER | c.1482-196A>G | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590305 | |||||||
| chr18:49590340 | G | A | 3 | a0002c0002t0022g0296 a0002c0002t0022g0302 a0002c0002t0066g0291 |
3 | HG02155.hp2 NA18964.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1482-161G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590340 | |||||||
| chr18:49590388 | T | C | 2 | a0001c0001t0039g0177 a0001c0001t0039g0183 |
2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1482-113T>C | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590388 | |||||||
| chr18:49590388 | TA | T | 6 | a0001c0001t0038g0045 a0001c0001t0038g0169 a0001c0001t0094g0050 others(3): Show |
6 | HG02071.hp1 HG02622.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1482-112delA | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590388 | |||||||
| chr18:49590450 | G | A | 12 | a0001c0001t0017g0274 a0001c0001t0017g0276 a0001c0001t0017g0277 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1482-51G>A | LIPG | ENSG00000101670.12 | transcript | ENST00000261292.9 | protein_coding | 9/9 | chr18 | 49590450 |