Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9710 |
| ensemblid | ENSG00000166398.14 |
| hgncid | 29016 |
| symbol | GARRE1 |
| name | granule associated Rac and RHOG effector 1 |
| refseq_nuc | NM_014686.5 |
| refseq_prot | NP_055501.2 |
| ensembl_nuc | ENST00000299505.8 |
| ensembl_prot | ENSP00000299505.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 34254554 |
| end | 34355566 |
| strand | + |
| ver | v1.2 |
| region | chr19:34254554-34355566 |
| region5000 | chr19:34249554-34360566 |
| regionname0 | GARRE1_chr19_34254554_34355566 |
| regionname5000 | GARRE1_chr19_34249554_34360566 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1070 | 313 | 88 | 58 | 123 | 12 | 30 | 91 | GARRE1_chr19_34249554_34360566 | GARRE1 | MYCCS others(1065): Show |
chr19 | 34249554 | 34360566 |
| a0002 | 0/0 | 1066 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | MYCCS others(1061): Show |
chr19 | 34249554 | 34360566 |
| a0003 | 0/0 | 1070 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | MYCCS others(1065): Show |
chr19 | 34249554 | 34360566 |
| a0004 | 0/0 | 1070 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | MYCCS others(1065): Show |
chr19 | 34249554 | 34360566 |
| a0005 | 0/0 | 1070 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | MYCCS others(1065): Show |
chr19 | 34249554 | 34360566 |
| a0006 | 0/0 | 1070 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | MYCCS others(1065): Show |
chr19 | 34249554 | 34360566 |
| a0007 | 0/0 | 1070 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | MYCCS others(1065): Show |
chr19 | 34249554 | 34360566 |
| a0008 | 0/0 | 1070 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | MYCCS others(1065): Show |
chr19 | 34249554 | 34360566 |
| a0009 | 0/0 | 1070 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | MYCCS others(1065): Show |
chr19 | 34249554 | 34360566 |
| a0010 | 0/0 | 1070 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | MYCCS others(1065): Show |
chr19 | 34249554 | 34360566 |
| a0011 | 0/0 | 1070 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | MYCCS others(1065): Show |
chr19 | 34249554 | 34360566 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3210 | 202 | 55 | 29 | 90 | 7 | 21 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 | ||
| a0001c0002 | 1/0 | 3210 | 107 | 30 | 29 | 33 | 5 | 9 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 | ||
| a0001c0004 | 0/0 | 3210 | 2 | 2 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 | ||
| a0001c0011 | 0/1 | 3210 | 1 | 0 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 | ||
| a0001c0012 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 | ||
| a0002c0003 | 0/0 | 3198 | 3 | 0 | 2 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3193): Show |
chr19 | 34249554 | 34360566 | ||
| a0003c0005 | 0/0 | 3210 | 2 | 0 | 0 | 0 | 0 | 2 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 | ||
| a0004c0010 | 0/0 | 3210 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 | ||
| a0005c0009 | 0/0 | 3210 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 | ||
| a0006c0014 | 0/0 | 3210 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 | ||
| a0007c0007 | 0/0 | 3210 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 | ||
| a0008c0008 | 0/0 | 3210 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 | ||
| a0009c0013 | 0/0 | 3210 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 | ||
| a0010c0015 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 | ||
| a0011c0006 | 0/0 | 3210 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | ATGTA others(3205): Show |
chr19 | 34249554 | 34360566 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6672 | 185 | 49 | 26 | 83 | 7 | 20 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0001t0005 | 0/0 | 6674 | 6 | 0 | 1 | 5 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6669): Show |
chr19 | 34249554 | 34360566 |
| a0001c0001t0007 | 0/0 | 6672 | 3 | 2 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0001t0009 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0001t0016 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0001t0017 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0001t0018 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0001t0019 | 0/0 | 6672 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0001t0020 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0001t0021 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0001t0022 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0002 | 1/0 | 6680 | 64 | 8 | 13 | 30 | 5 | 7 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6675): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0003 | 0/0 | 6680 | 16 | 4 | 12 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6675): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0004 | 0/0 | 6672 | 10 | 10 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0006 | 0/0 | 6672 | 3 | 3 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0008 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0009 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0010 | 0/0 | 6680 | 2 | 0 | 0 | 2 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6675): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0011 | 0/0 | 6680 | 2 | 1 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6675): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0013 | 0/0 | 6680 | 2 | 0 | 2 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6675): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0014 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0015 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0023 | 0/0 | 6686 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6681): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0024 | 0/0 | 6680 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6675): Show |
chr19 | 34249554 | 34360566 |
| a0001c0002t0025 | 0/0 | 6680 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6675): Show |
chr19 | 34249554 | 34360566 |
| a0001c0004t0002 | 0/0 | 6680 | 2 | 2 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6675): Show |
chr19 | 34249554 | 34360566 |
| a0001c0011t0001 | 0/1 | 6672 | 1 | 0 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0001c0012t0001 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0002c0003t0003 | 0/0 | 6668 | 3 | 0 | 2 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6663): Show |
chr19 | 34249554 | 34360566 |
| a0003c0005t0012 | 0/0 | 6686 | 2 | 0 | 0 | 0 | 0 | 2 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6681): Show |
chr19 | 34249554 | 34360566 |
| a0004c0010t0001 | 0/0 | 6672 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0005c0009t0001 | 0/0 | 6672 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0006c0014t0001 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0007c0007t0001 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0008c0008t0001 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0009c0013t0001 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0010c0015t0001 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| a0011c0006t0001 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | GTAAC others(6667): Show |
chr19 | 34249554 | 34360566 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0009g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0016g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0017g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0018g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0019g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0020g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0021g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0001t0022g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0002g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0009g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0010g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0010g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0011g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0011g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0013g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0013g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0015g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0023g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0024g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0002t0025g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0004t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0004t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0011t0001g0191 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0001c0012t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0002c0003t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0002c0003t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0002c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0003c0005t0012g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0003c0005t0012g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0004c0010t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0005c0009t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0006c0014t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0007c0007t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0008c0008t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0009c0013t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0010c0015t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| a0011c0006t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0045 | EUR | GBR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | GBR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | FIN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0042 | EUR | FIN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00423 | hp1 | a0001 | c0002 | t0010 | g0048 | EAS | CHS | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | CHS | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0036 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0031 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0168 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0170 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0164 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01081 | hp1 | a0001 | c0001 | t0019 | g0308 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01099 | hp1 | a0001 | c0002 | t0024 | g0043 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01099 | hp2 | a0004 | c0010 | t0001 | g0189 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01168 | hp1 | a0002 | c0003 | t0003 | g0155 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0034 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01169 | hp1 | a0002 | c0003 | t0003 | g0156 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01256 | hp2 | a0001 | c0002 | t0013 | g0020 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01258 | hp1 | a0001 | c0002 | t0013 | g0019 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0224 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0171 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0167 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0163 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0301 | EUR | IBS | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0037 | EUR | IBS | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0162 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01978 | hp1 | a0001 | c0002 | t0003 | g0165 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01981 | hp1 | a0001 | c0002 | t0011 | g0007 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0166 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0161 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0152 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02132 | hp2 | a0001 | c0001 | t0009 | g0226 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0169 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0070 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0172 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02300 | hp2 | a0005 | c0009 | t0001 | g0229 | AMR | PEL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02451 | hp2 | a0001 | c0002 | t0015 | g0174 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02572 | hp1 | a0001 | c0002 | t0014 | g0071 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02602 | hp1 | a0002 | c0003 | t0003 | g0157 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02615 | hp2 | a0001 | c0001 | t0017 | g0002 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0058 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02683 | hp1 | a0006 | c0014 | t0001 | g0304 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02683 | hp2 | a0003 | c0005 | t0012 | g0319 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0067 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0068 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02717 | hp2 | a0001 | c0002 | t0008 | g0160 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0084 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02809 | hp1 | a0001 | c0001 | t0021 | g0188 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02809 | hp2 | a0001 | c0002 | t0006 | g0150 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02818 | hp1 | a0001 | c0002 | t0004 | g0074 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02818 | hp2 | a0001 | c0002 | t0006 | g0149 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0075 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02897 | hp1 | a0001 | c0002 | t0004 | g0076 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0078 | AFR | ESN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02922 | hp2 | a0001 | c0004 | t0002 | g0015 | AFR | ESN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0083 | AFR | ESN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02965 | hp2 | a0001 | c0002 | t0008 | g0079 | AFR | ESN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0077 | AFR | ESN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03017 | hp2 | a0001 | c0002 | t0025 | g0035 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0069 | AFR | ESN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0158 | AFR | MSL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03209 | hp2 | a0001 | c0012 | t0001 | g0141 | AFR | MSL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0154 | AFR | MSL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03239 | hp1 | a0007 | c0007 | t0001 | g0255 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0014 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03486 | hp1 | a0001 | c0002 | t0003 | g0153 | AFR | MSL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0038 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0056 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03516 | hp2 | a0001 | c0001 | t0022 | g0147 | AFR | ESN | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | BEB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG03942 | hp2 | a0008 | c0008 | t0001 | g0318 | SAS | BEB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG04115 | hp2 | a0009 | c0013 | t0001 | g0128 | SAS | STU | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0064 | SAS | BEB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0133 | SAS | STU | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG04204 | hp1 | a0003 | c0005 | t0012 | g0320 | SAS | STU | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG04204 | hp2 | a0001 | c0002 | t0023 | g0050 | SAS | STU | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | CHB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | YRI | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18940 | hp1 | a0001 | c0002 | t0009 | g0230 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18970 | hp2 | a0010 | c0015 | t0001 | g0281 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18988 | hp1 | a0001 | c0001 | t0018 | g0264 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0223 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19009 | hp2 | a0001 | c0002 | t0010 | g0029 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0061 | AFR | LWK | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19030 | hp2 | a0001 | c0002 | t0006 | g0151 | AFR | LWK | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0220 | EAS | JPT | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19240 | hp1 | a0001 | c0001 | t0016 | g0143 | AFR | YRI | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA19240 | hp2 | a0001 | c0004 | t0002 | g0033 | AFR | YRI | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | ASW | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0072 | AFR | ASW | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | TSI | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0039 | EUR | TSI | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0018 | EUR | TSI | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA20905 | hp1 | a0001 | c0001 | t0020 | g0283 | SAS | GIH | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA20905 | hp2 | a0011 | c0006 | t0001 | g0121 | SAS | GIH | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0049 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG01123 | hp2 | a0001 | c0001 | t0007 | g0146 | AMR | CLM | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0073 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02486 | hp1 | a0001 | c0002 | t0011 | g0005 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | USA | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | USA | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | USA | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | USA | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | LWK | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| homoSapiens | chm13v2 | a0001 | c0011 | t0001 | g0191 | REF | REF | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0263 | REF | REF | GARRE1_chr19_34249554_34360566 | GARRE1 | chr19 | 34249554 | 34360566 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:34300498 | A | G | 1 | a0010 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.25A>G | p.Ser9Gly | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/14 | 881/6680 | 25/3213 | 9/1070 | chr19 | 34300498 | |||
| chr19:34300591 | G | A | 1 | a0011 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.118G>A | p.Ala40Thr | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/14 | 974/6680 | 118/3213 | 40/1070 | chr19 | 34300591 | |||
| chr19:34328150 | C | T | 1 | a0006 | 1 | HG02683.hp1 | missense_variant&splice_region_variant | MODERATE | c.1103C>T | p.Thr368Met | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/14 | 1959/6680 | 1103/3213 | 368/1070 | chr19 | 34328150 | |||
| chr19:34341559 | G | A | 1 | a0007 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.1625G>A | p.Arg542Gln | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/14 | 2481/6680 | 1625/3213 | 542/1070 | chr19 | 34341559 | |||
| chr19:34342041 | C | T | 1 | a0009 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.2107C>T | p.Pro703Ser | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/14 | 2963/6680 | 2107/3213 | 703/1070 | chr19 | 34342041 | |||
| chr19:34342156 | T | C | 1 | a0008 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.2222T>C | p.Ile741Thr | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/14 | 3078/6680 | 2222/3213 | 741/1070 | chr19 | 34342156 | |||
| chr19:34342174 | C | T | 1 | a0003 | 2 | HG02683.hp2 HG04204.hp1 |
missense_variant | MODERATE | c.2240C>T | p.Pro747Leu | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/14 | 3096/6680 | 2240/3213 | 747/1070 | chr19 | 34342174 | |||
| chr19:34349112 | G | C | 1 | a0005 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.2784G>C | p.Met928Ile | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/14 | 3640/6680 | 2784/3213 | 928/1070 | chr19 | 34349112 | |||
| chr19:34352806 | G | A | 1 | a0004 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.3064G>A | p.Ala1022Thr | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 3920/6680 | 3064/3213 | 1022/1070 | chr19 | 34352806 | |||
| chr19:34352848 | ACCCCACC others(5): Show |
A | 1 | a0002 | 3 | HG01168.hp1 HG01169.hp1 HG02602.hp1 |
disruptive_inframe_deletion | MODERATE | c.3116_3127delAGCCCC others(6): Show |
p.Gln1039_Pro1042del | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 3972/6680 | 3116/3213 | 1039/1070 | INFO_REALIGN_3_PRIME | chr19 | 34352848 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:34300581 | G | A | 1 | a0001c0004 | 2 | HG02922.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.108G>A | p.Glu36Glu | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/14 | 964/6680 | 108/3213 | 36/1070 | chr19 | 34300581 | |||
| chr19:34341842 | G | A | 1 | a0002c0003 | 3 | HG01168.hp1 HG01169.hp1 HG02602.hp1 |
synonymous_variant | LOW | c.1908G>A | p.Lys636Lys | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/14 | 2764/6680 | 1908/3213 | 636/1070 | chr19 | 34341842 | |||
| chr19:34351583 | T | C | 11 | a0001c0001 a0001c0012 a0003c0005 others(8): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
synonymous_variant | LOW | c.2895T>C | p.Asp965Asp | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 13/14 | 3751/6680 | 2895/3213 | 965/1070 | chr19 | 34351583 | |||
| chr19:34351589 | C | T | 1 | a0001c0012 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2901C>T | p.Asn967Asn | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 13/14 | 3757/6680 | 2901/3213 | 967/1070 | chr19 | 34351589 | |||
| chr19:34352856 | C | A | 11 | a0001c0001 a0001c0002 a0003c0005 others(8): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
synonymous_variant | LOW | c.3114C>A | p.Pro1038Pro | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 3970/6680 | 3114/3213 | 1038/1070 | chr19 | 34352856 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:34299712 | G | A | 5 | a0001c0002t0004 a0001c0002t0006 a0001c0002t0008 others(2): Show |
17 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-762G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/14 | 762 | chr19 | 34299712 | ||||||
| chr19:34299823 | C | T | 1 | a0001c0002t0025 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-651C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/14 | 651 | chr19 | 34299823 | ||||||
| chr19:34299944 | G | T | 1 | a0001c0002t0013 | 2 | HG01256.hp2 HG01258.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-530G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/14 | chr19 | 34299944 | |||||||
| chr19:34299967 | G | A | 1 | a0001c0001t0016 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-507G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/14 | 507 | chr19 | 34299967 | ||||||
| chr19:34352969 | A | T | 1 | a0003c0005t0012 | 2 | HG02683.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*14A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 14 | chr19 | 34352969 | ||||||
| chr19:34352969 | AGCCTGCC others(1): Show |
A | 26 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(23): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*30_*37delTGCCTGCC | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 30 | INFO_REALIGN_3_PRIME | chr19 | 34352969 | |||||
| chr19:34353015 | T | C | 1 | a0001c0002t0010 | 2 | HG00423.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*60T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 60 | chr19 | 34353015 | ||||||
| chr19:34353089 | C | G | 1 | a0001c0002t0011 | 2 | HG01981.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*134C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 134 | chr19 | 34353089 | ||||||
| chr19:34353230 | G | A | 1 | a0001c0001t0017 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*275G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 275 | chr19 | 34353230 | ||||||
| chr19:34353397 | C | G | 2 | a0001c0001t0007 a0001c0001t0022 |
4 | HG01123.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*442C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 442 | chr19 | 34353397 | ||||||
| chr19:34353501 | G | C | 1 | a0001c0001t0018 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*546G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 546 | chr19 | 34353501 | ||||||
| chr19:34353584 | C | T | 1 | a0001c0002t0024 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*629C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 629 | chr19 | 34353584 | ||||||
| chr19:34353638 | G | C | 1 | a0001c0002t0006 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*683G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 683 | chr19 | 34353638 | ||||||
| chr19:34353658 | T | G | 27 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(24): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*703T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 703 | chr19 | 34353658 | ||||||
| chr19:34353705 | C | T | 1 | a0001c0001t0021 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*750C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 750 | chr19 | 34353705 | ||||||
| chr19:34353800 | A | G | 1 | a0001c0001t0020 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*845A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 845 | chr19 | 34353800 | ||||||
| chr19:34353821 | G | A | 1 | a0001c0002t0014 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*866G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 866 | chr19 | 34353821 | ||||||
| chr19:34354398 | G | A | 2 | a0001c0002t0004 a0001c0002t0014 |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1443G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 1443 | chr19 | 34354398 | ||||||
| chr19:34354402 | T | G | 5 | a0001c0002t0004 a0001c0002t0006 a0001c0002t0008 others(2): Show |
17 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1447T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 1447 | chr19 | 34354402 | ||||||
| chr19:34354528 | C | T | 1 | a0001c0002t0015 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1573C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 1573 | chr19 | 34354528 | ||||||
| chr19:34354649 | G | C | 1 | a0001c0001t0022 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1694G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 1694 | chr19 | 34354649 | ||||||
| chr19:34354674 | C | A | 28 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(25): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1719C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 1719 | chr19 | 34354674 | ||||||
| chr19:34354691 | A | AAT | 1 | a0001c0001t0005 | 6 | HG01261.hp1 HG02080.hp2 NA18960.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1747_*1748dupAT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 1749 | INFO_REALIGN_3_PRIME | chr19 | 34354691 | |||||
| chr19:34354700 | A | ATATATG | 2 | a0001c0002t0023 a0003c0005t0012 |
3 | HG02683.hp2 HG04204.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1748_*1749insATGT others(2): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 1749 | INFO_REALIGN_3_PRIME | chr19 | 34354700 | |||||
| chr19:34354750 | G | A | 1 | a0001c0001t0019 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1795G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 1795 | chr19 | 34354750 | ||||||
| chr19:34355051 | A | G | 2 | a0001c0002t0004 a0001c0002t0014 |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2096A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 14/14 | 2096 | chr19 | 34355051 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:34254639 | A | AGGCGGGG others(7): Show |
1 | a0001c0001t0017g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-796+33_-796+46dup others(14): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34254639 | ||||||
| chr19:34254647 | G | T | 1 | a0001c0001t0001g0325 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-796+33G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34254647 | |||||||
| chr19:34254786 | C | G | 4 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(1): Show |
4 | NA18945.hp2 NA18971.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.-796+172C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34254786 | |||||||
| chr19:34254921 | C | T | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-796+307C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34254921 | |||||||
| chr19:34254923 | C | G | 2 | a0001c0001t0001g0317 a0008c0008t0001g0318 |
2 | HG00639.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-796+309C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34254923 | |||||||
| chr19:34255181 | AG | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(214): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.-796+571delG | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34255181 | ||||||
| chr19:34255303 | C | G | 1 | a0001c0001t0001g0316 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-796+689C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34255303 | |||||||
| chr19:34255632 | C | A | 65 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(62): Show |
65 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-796+1018C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34255632 | |||||||
| chr19:34255668 | A | G | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-796+1054A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34255668 | |||||||
| chr19:34255673 | C | CT | 18 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(15): Show |
18 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-796+1075dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34255673 | ||||||
| chr19:34255673 | CT | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(213): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.-796+1075delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34255673 | ||||||
| chr19:34255844 | CTTTA | C | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-796+1234_-796+123 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34255844 | ||||||
| chr19:34255893 | G | A | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-796+1279G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34255893 | |||||||
| chr19:34255995 | C | A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-796+1381C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34255995 | |||||||
| chr19:34256126 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-796+1512A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34256126 | |||||||
| chr19:34256149 | A | G | 12 | a0001c0002t0003g0161 a0001c0002t0003g0162 a0001c0002t0003g0163 others(9): Show |
12 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-796+1535A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34256149 | |||||||
| chr19:34256226 | T | C | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-796+1612T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34256226 | |||||||
| chr19:34256328 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(72): Show |
76 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-796+1714G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34256328 | |||||||
| chr19:34256450 | G | A | 5 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(2): Show |
5 | HG00639.hp2 HG01978.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-796+1836G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34256450 | |||||||
| chr19:34256519 | C | CA | 22 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0216 others(19): Show |
22 | HG01361.hp1 HG02074.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-796+1920dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34256519 | ||||||
| chr19:34257086 | G | A | 7 | a0001c0001t0001g0225 a0001c0001t0005g0219 a0001c0001t0005g0220 others(4): Show |
7 | HG01261.hp1 HG02027.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-796+2472G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34257086 | |||||||
| chr19:34257160 | C | CT | 37 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(34): Show |
37 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-796+2560dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34257160 | ||||||
| chr19:34257160 | CT | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(84): Show |
88 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-796+2560delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34257160 | ||||||
| chr19:34257160 | CTT | C | 95 | a0001c0001t0001g0082 a0001c0002t0002g0003 a0001c0002t0002g0004 others(92): Show |
95 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-796+2559_-796+256 others(6): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34257160 | ||||||
| chr19:34257163 | T | C | 84 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(81): Show |
84 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-796+2549T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34257163 | |||||||
| chr19:34257214 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-796+2600G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34257214 | |||||||
| chr19:34257231 | C | T | 1 | a0001c0002t0003g0172 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-796+2617C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34257231 | |||||||
| chr19:34257239 | C | T | 1 | a0001c0002t0002g0067 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-796+2625C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34257239 | |||||||
| chr19:34257507 | A | ACTCT | 219 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-796+2894_-796+289 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34257507 | ||||||
| chr19:34257544 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-796+2930A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34257544 | |||||||
| chr19:34257878 | CTTTTTCT others(2): Show |
C | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-796+3279_-796+328 others(13): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34257878 | ||||||
| chr19:34257893 | C | CT | 6 | a0001c0001t0001g0145 a0001c0002t0008g0079 a0001c0002t0008g0160 others(3): Show |
6 | HG02451.hp2 HG02683.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-796+3293dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34257893 | ||||||
| chr19:34258156 | C | T | 2 | a0001c0002t0008g0160 a0001c0002t0015g0174 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-796+3542C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34258156 | |||||||
| chr19:34258305 | C | T | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-796+3691C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34258305 | |||||||
| chr19:34258437 | T | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(73): Show |
77 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-796+3823T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34258437 | |||||||
| chr19:34258455 | CA | C | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-796+3842delA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34258455 | |||||||
| chr19:34258507 | G | A | 3 | a0001c0002t0015g0174 a0003c0005t0012g0319 a0003c0005t0012g0320 |
3 | HG02451.hp2 HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-796+3893G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34258507 | |||||||
| chr19:34258511 | G | A | 4 | a0001c0001t0007g0083 a0001c0001t0007g0084 a0001c0001t0007g0146 others(1): Show |
4 | HG01123.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-796+3897G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34258511 | |||||||
| chr19:34258538 | A | G | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-796+3924A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34258538 | |||||||
| chr19:34258651 | A | G | 1 | a0001c0002t0003g0171 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-796+4037A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34258651 | |||||||
| chr19:34258662 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-796+4048C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34258662 | |||||||
| chr19:34258717 | G | C | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-796+4103G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34258717 | |||||||
| chr19:34258744 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(72): Show |
76 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-796+4130C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34258744 | |||||||
| chr19:34258789 | C | CA | 86 | a0001c0001t0001g0159 a0001c0001t0009g0226 a0001c0002t0002g0003 others(83): Show |
86 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-796+4186dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34258789 | ||||||
| chr19:34258805 | A | G | 1 | a0001c0002t0004g0078 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-796+4191A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34258805 | |||||||
| chr19:34259239 | G | A | 1 | a0001c0002t0004g0078 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-796+4625G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34259239 | |||||||
| chr19:34259654 | T | G | 3 | a0001c0001t0001g0227 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | NA18962.hp1 NA18965.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-796+5040T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34259654 | |||||||
| chr19:34259662 | G | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.-796+5048G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34259662 | |||||||
| chr19:34259758 | A | G | 1 | a0001c0002t0004g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-796+5144A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34259758 | |||||||
| chr19:34260041 | C | G | 1 | a0001c0002t0004g0078 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-796+5427C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34260041 | |||||||
| chr19:34260168 | C | T | 1 | a0001c0002t0002g0066 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-796+5554C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34260168 | |||||||
| chr19:34260179 | C | T | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-796+5565C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34260179 | |||||||
| chr19:34260195 | C | G | 2 | a0001c0002t0004g0075 a0001c0002t0004g0076 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-796+5581C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34260195 | |||||||
| chr19:34260401 | C | A | 84 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(81): Show |
84 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-796+5787C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34260401 | |||||||
| chr19:34260521 | CA | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(72): Show |
76 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-796+5908delA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34260521 | |||||||
| chr19:34260564 | G | C | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-796+5950G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34260564 | |||||||
| chr19:34260684 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-796+6070C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34260684 | |||||||
| chr19:34260907 | G | A | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-796+6293G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34260907 | |||||||
| chr19:34260934 | T | TG | 6 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0233 others(3): Show |
6 | HG00642.hp2 HG02080.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-796+6324dupG | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34260934 | ||||||
| chr19:34261144 | G | A | 85 | a0001c0001t0001g0159 a0001c0002t0002g0003 a0001c0002t0002g0004 others(82): Show |
85 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-796+6530G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34261144 | |||||||
| chr19:34261224 | G | A | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-796+6610G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34261224 | |||||||
| chr19:34261550 | C | T | 1 | a0001c0002t0002g0148 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-796+6936C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34261550 | |||||||
| chr19:34261637 | G | A | 19 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(16): Show |
19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-796+7023G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34261637 | |||||||
| chr19:34261655 | A | G | 2 | a0001c0002t0004g0073 a0001c0002t0004g0074 |
2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-796+7041A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34261655 | |||||||
| chr19:34261666 | A | C | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-796+7052A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34261666 | |||||||
| chr19:34261939 | T | TA | 14 | a0001c0001t0001g0228 a0001c0001t0001g0235 a0001c0001t0001g0236 others(11): Show |
14 | HG00621.hp1 NA18747.hp2 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.-796+7326dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34261939 | ||||||
| chr19:34262002 | G | T | 1 | a0001c0001t0001g0298 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-796+7388G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34262002 | |||||||
| chr19:34262237 | T | C | 1 | a0001c0002t0003g0161 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-796+7623T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34262237 | |||||||
| chr19:34262287 | C | CT | 41 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0129 others(38): Show |
41 | HG00621.hp1 HG01261.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.-796+7701dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | C | CTT | 31 | a0001c0001t0001g0081 a0001c0001t0001g0139 a0001c0001t0001g0140 others(28): Show |
31 | HG00733.hp2 HG01099.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.-796+7700_-796+770 others(6): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | C | CTTT | 25 | a0001c0001t0001g0144 a0001c0001t0001g0175 a0001c0001t0001g0177 others(22): Show |
25 | HG00642.hp2 HG01074.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.-796+7699_-796+770 others(7): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | C | CTTTT | 6 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0297 others(3): Show |
6 | HG01358.hp2 HG02055.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-796+7698_-796+770 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | C | CTTTTTTT others(2): Show |
6 | a0001c0002t0003g0163 a0001c0002t0003g0164 a0001c0002t0003g0165 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-796+7693_-796+770 others(13): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | C | CTTTTTTT others(3): Show |
4 | a0001c0002t0003g0152 a0001c0002t0003g0167 a0001c0002t0003g0168 others(1): Show |
4 | HG00738.hp2 HG01261.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.-796+7692_-796+770 others(14): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | C | CTTTTTTT others(4): Show |
21 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(18): Show |
21 | HG00597.hp2 HG01168.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.-796+7691_-796+770 others(15): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | C | CTTTTTTT others(5): Show |
29 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0024 others(26): Show |
29 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.-796+7690_-796+770 others(16): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | C | CTTTTTTT others(6): Show |
8 | a0001c0002t0002g0049 a0001c0002t0002g0051 a0001c0002t0002g0052 others(5): Show |
8 | HG00423.hp1 HG01123.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-796+7689_-796+770 others(17): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | C | CTTTTTTT others(7): Show |
4 | a0001c0002t0002g0055 a0001c0002t0002g0056 a0001c0002t0002g0057 others(1): Show |
4 | HG01074.hp2 HG02698.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-796+7688_-796+770 others(18): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | C | CTTTTTTT others(8): Show |
5 | a0001c0001t0001g0159 a0001c0002t0002g0008 a0001c0002t0002g0058 others(2): Show |
5 | HG01361.hp1 HG02630.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.-796+7687_-796+770 others(19): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | C | CTTTTTTT others(9): Show |
2 | a0001c0002t0002g0061 a0001c0002t0002g0062 |
2 | NA18950.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-796+7686_-796+770 others(20): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | C | CTTTTTTT others(11): Show |
2 | a0001c0002t0002g0063 a0001c0002t0002g0064 |
2 | HG04184.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-796+7684_-796+770 others(22): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | C | CTTTTTTT others(12): Show |
1 | a0001c0002t0002g0065 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-796+7683_-796+770 others(23): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | CT | C | 11 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0235 others(8): Show |
11 | HG02074.hp1 NA18950.hp2 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.-796+7701delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262287 | CTTTTTTT others(9): Show |
C | 1 | a0001c0002t0004g0078 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-796+7686_-796+770 others(20): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34262287 | ||||||
| chr19:34262511 | G | A | 1 | a0001c0002t0004g0078 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-796+7897G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34262511 | |||||||
| chr19:34262526 | C | T | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-796+7912C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34262526 | |||||||
| chr19:34262555 | C | G | 3 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | HG01257.hp1 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-796+7941C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34262555 | |||||||
| chr19:34262706 | G | T | 1 | a0001c0002t0015g0174 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-796+8092G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34262706 | |||||||
| chr19:34262736 | T | C | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-796+8122T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34262736 | |||||||
| chr19:34262784 | G | A | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-796+8170G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34262784 | |||||||
| chr19:34262922 | A | T | 1 | a0001c0001t0001g0289 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-796+8308A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34262922 | |||||||
| chr19:34263049 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | NA18986.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-796+8435C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34263049 | |||||||
| chr19:34263258 | C | T | 2 | a0001c0002t0002g0125 a0001c0002t0002g0138 |
2 | NA19066.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-796+8644C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34263258 | |||||||
| chr19:34263265 | G | GAGAT | 72 | a0001c0001t0001g0080 a0001c0001t0001g0111 a0001c0001t0001g0113 others(69): Show |
72 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.-796+8685_-796+868 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34263265 | ||||||
| chr19:34263265 | G | GAGATAGA others(1): Show |
71 | a0001c0001t0001g0001 a0001c0001t0001g0085 a0001c0001t0001g0088 others(68): Show |
72 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-796+8681_-796+868 others(12): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34263265 | ||||||
| chr19:34263265 | G | GAGATAGA others(5): Show |
4 | a0001c0001t0001g0087 a0001c0001t0001g0126 a0001c0002t0002g0009 others(1): Show |
4 | HG00597.hp2 HG01109.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-796+8677_-796+868 others(16): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34263265 | ||||||
| chr19:34263265 | G | GAGATAGA others(9): Show |
1 | a0001c0002t0002g0173 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-796+8673_-796+868 others(20): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34263265 | ||||||
| chr19:34263265 | GAGAT | G | 28 | a0001c0001t0001g0190 a0001c0001t0001g0215 a0001c0001t0001g0228 others(25): Show |
28 | HG00099.hp1 HG00621.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-796+8685_-796+868 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34263265 | ||||||
| chr19:34263265 | GAGATAGA others(1): Show |
G | 4 | a0001c0001t0001g0081 a0001c0001t0001g0212 a0001c0002t0002g0046 others(1): Show |
4 | HG02040.hp2 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-796+8681_-796+868 others(12): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34263265 | ||||||
| chr19:34263269 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-796+8655T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34263269 | |||||||
| chr19:34263297 | T | TAGATAGA others(5): Show |
4 | a0001c0002t0002g0010 a0001c0002t0002g0024 a0001c0002t0002g0025 others(1): Show |
4 | HG02027.hp1 HG02083.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-796+8688_-796+868 others(16): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34263297 | ||||||
| chr19:34263436 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-796+8822T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34263436 | |||||||
| chr19:34263482 | C | CT | 6 | a0001c0001t0005g0219 a0001c0001t0005g0220 a0001c0001t0005g0221 others(3): Show |
6 | HG02080.hp2 HG02965.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.-796+8881dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34263482 | ||||||
| chr19:34263558 | A | G | 1 | a0001c0002t0002g0058 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-796+8944A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34263558 | |||||||
| chr19:34263627 | G | A | 18 | a0001c0001t0001g0256 a0001c0001t0001g0299 a0001c0001t0001g0300 others(15): Show |
18 | HG00140.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.-796+9013G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34263627 | |||||||
| chr19:34263892 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(214): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.-796+9278G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34263892 | |||||||
| chr19:34264415 | G | C | 1 | a0001c0001t0001g0120 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-796+9801G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34264415 | |||||||
| chr19:34264421 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(166): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-796+9807C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34264421 | |||||||
| chr19:34264427 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-796+9813C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34264427 | |||||||
| chr19:34264493 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-796+9879G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34264493 | |||||||
| chr19:34264517 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-796+9903G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34264517 | |||||||
| chr19:34264538 | A | G | 2 | a0001c0001t0020g0283 a0007c0007t0001g0255 |
2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-796+9924A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34264538 | |||||||
| chr19:34264640 | C | T | 1 | a0001c0002t0008g0160 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-796+10026C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34264640 | |||||||
| chr19:34264645 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-796+10031A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34264645 | |||||||
| chr19:34264818 | G | C | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-796+10204G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34264818 | |||||||
| chr19:34264906 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-796+10292C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34264906 | |||||||
| chr19:34265019 | T | C | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-796+10405T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34265019 | |||||||
| chr19:34265219 | C | T | 1 | a0001c0002t0011g0007 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-796+10605C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34265219 | |||||||
| chr19:34265273 | T | C | 5 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0075 others(2): Show |
5 | HG02572.hp1 HG02717.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-796+10659T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34265273 | |||||||
| chr19:34265293 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-796+10679C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34265293 | |||||||
| chr19:34265311 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-796+10697A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34265311 | |||||||
| chr19:34265340 | C | A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-796+10726C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34265340 | |||||||
| chr19:34265776 | T | A | 1 | a0001c0002t0002g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-796+11162T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34265776 | |||||||
| chr19:34265948 | G | A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-796+11334G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34265948 | |||||||
| chr19:34266035 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-796+11421G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34266035 | |||||||
| chr19:34266122 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-796+11508G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34266122 | |||||||
| chr19:34266319 | A | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-796+11705A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34266319 | |||||||
| chr19:34266426 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-796+11812A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34266426 | |||||||
| chr19:34266558 | C | T | 4 | a0001c0001t0001g0175 a0001c0001t0001g0192 a0001c0001t0001g0209 others(1): Show |
4 | HG01099.hp2 HG02055.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-796+11944C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34266558 | |||||||
| chr19:34266756 | C | A | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-796+12142C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34266756 | |||||||
| chr19:34266811 | CCTT | C | 101 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(98): Show |
101 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-796+12200_-796+12 others(9): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34266811 | ||||||
| chr19:34267067 | C | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG00140.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-796+12453C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34267067 | |||||||
| chr19:34267125 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-796+12511G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34267125 | |||||||
| chr19:34267157 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-796+12543T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34267157 | |||||||
| chr19:34267197 | C | G | 1 | a0001c0002t0002g0026 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-796+12583C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34267197 | |||||||
| chr19:34267214 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-796+12600G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34267214 | |||||||
| chr19:34267354 | A | C | 66 | a0001c0001t0009g0226 a0001c0002t0002g0003 a0001c0002t0002g0004 others(63): Show |
66 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.-796+12740A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34267354 | |||||||
| chr19:34267495 | C | T | 4 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 others(1): Show |
4 | HG02809.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-796+12881C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34267495 | |||||||
| chr19:34267721 | A | AT | 37 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(34): Show |
37 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-796+13118dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34267721 | ||||||
| chr19:34267780 | G | GT | 6 | a0001c0001t0001g0085 a0001c0001t0001g0108 a0001c0001t0001g0126 others(3): Show |
6 | HG01891.hp1 HG01981.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-796+13179dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34267780 | ||||||
| chr19:34267780 | G | T | 1 | a0001c0002t0002g0047 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-796+13166G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34267780 | |||||||
| chr19:34267804 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-796+13190C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34267804 | |||||||
| chr19:34267859 | T | G | 1 | a0001c0001t0001g0315 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-796+13245T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34267859 | |||||||
| chr19:34268078 | G | GT | 23 | a0001c0001t0001g0215 a0001c0001t0001g0228 a0001c0001t0001g0235 others(20): Show |
23 | HG00621.hp1 HG01168.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.-796+13477dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34268078 | ||||||
| chr19:34268224 | A | T | 1 | a0001c0002t0002g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-796+13610A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34268224 | |||||||
| chr19:34268233 | G | A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-796+13619G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34268233 | |||||||
| chr19:34268629 | G | C | 1 | a0001c0002t0002g0065 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-796+14015G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34268629 | |||||||
| chr19:34268724 | G | A | 1 | a0011c0006t0001g0121 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-796+14110G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34268724 | |||||||
| chr19:34268726 | C | T | 1 | a0001c0002t0004g0078 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-796+14112C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34268726 | |||||||
| chr19:34268889 | A | G | 1 | a0001c0002t0002g0006 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-796+14275A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34268889 | |||||||
| chr19:34269058 | G | A | 4 | a0001c0002t0002g0018 a0001c0002t0002g0034 a0001c0002t0013g0019 others(1): Show |
4 | HG01168.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-796+14444G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34269058 | |||||||
| chr19:34269131 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-796+14517A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34269131 | |||||||
| chr19:34269234 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-796+14620C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34269234 | |||||||
| chr19:34269286 | G | C | 1 | a0001c0002t0003g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-796+14672G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34269286 | |||||||
| chr19:34269473 | G | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(257): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.-796+14859G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34269473 | |||||||
| chr19:34269646 | A | G | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-796+15032A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34269646 | |||||||
| chr19:34269683 | C | T | 2 | a0001c0002t0002g0125 a0001c0002t0002g0138 |
2 | NA19066.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-796+15069C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34269683 | |||||||
| chr19:34269893 | T | C | 1 | a0001c0002t0002g0026 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-796+15279T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34269893 | |||||||
| chr19:34269972 | C | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0085 others(59): Show |
63 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.-796+15358C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34269972 | |||||||
| chr19:34270031 | C | G | 53 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(50): Show |
53 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.-796+15417C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34270031 | |||||||
| chr19:34270482 | G | C | 1 | a0001c0001t0001g0291 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-796+15868G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34270482 | |||||||
| chr19:34270508 | G | A | 7 | a0001c0001t0001g0081 a0001c0001t0001g0139 a0001c0001t0001g0140 others(4): Show |
7 | HG02886.hp1 HG02976.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-796+15894G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34270508 | |||||||
| chr19:34270562 | A | G | 1 | a0001c0002t0011g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-796+15948A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34270562 | |||||||
| chr19:34270707 | A | T | 1 | a0001c0001t0001g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-796+16093A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34270707 | |||||||
| chr19:34270933 | A | G | 5 | a0001c0001t0001g0085 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
5 | HG00423.hp2 HG00609.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.-796+16319A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34270933 | |||||||
| chr19:34270973 | A | G | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-796+16359A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34270973 | |||||||
| chr19:34271007 | G | A | 2 | a0001c0002t0004g0070 a0001c0002t0004g0072 |
2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-796+16393G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34271007 | |||||||
| chr19:34271245 | CT | C | 17 | a0001c0001t0001g0082 a0001c0001t0001g0089 a0001c0001t0001g0090 others(14): Show |
17 | HG00099.hp2 HG00609.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-796+16653delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34271245 | ||||||
| chr19:34271252 | T | C | 1 | a0001c0002t0015g0174 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-796+16638T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34271252 | |||||||
| chr19:34271401 | A | C | 2 | a0001c0001t0020g0283 a0007c0007t0001g0255 |
2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-796+16787A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34271401 | |||||||
| chr19:34271530 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-796+16916G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34271530 | |||||||
| chr19:34271544 | G | A | 1 | a0001c0002t0025g0035 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-796+16930G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34271544 | |||||||
| chr19:34271588 | C | T | 1 | a0010c0015t0001g0281 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-796+16974C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34271588 | |||||||
| chr19:34271827 | TCAAAAA | T | 18 | a0001c0001t0001g0259 a0001c0002t0004g0068 a0001c0002t0004g0069 others(15): Show |
18 | HG01993.hp1 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-796+17238_-796+17 others(12): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34271827 | ||||||
| chr19:34271834 | C | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-796+17220C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34271834 | |||||||
| chr19:34272301 | C | T | 1 | a0001c0002t0025g0035 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-796+17687C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34272301 | |||||||
| chr19:34272333 | G | A | 1 | a0001c0002t0002g0026 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-796+17719G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34272333 | |||||||
| chr19:34272532 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-796+17918A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34272532 | |||||||
| chr19:34273072 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-796+18458C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34273072 | |||||||
| chr19:34273096 | G | A | 15 | a0001c0002t0002g0010 a0001c0002t0002g0012 a0001c0002t0002g0021 others(12): Show |
15 | HG00733.hp1 HG02027.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-796+18482G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34273096 | |||||||
| chr19:34273098 | A | AG | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-796+18486dupG | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34273098 | ||||||
| chr19:34273259 | C | G | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-796+18645C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34273259 | |||||||
| chr19:34273300 | T | C | 19 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(16): Show |
19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-796+18686T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34273300 | |||||||
| chr19:34273315 | A | G | 5 | a0001c0001t0001g0085 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
5 | HG00423.hp2 HG00609.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.-796+18701A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34273315 | |||||||
| chr19:34273323 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-796+18709T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34273323 | |||||||
| chr19:34273391 | T | C | 2 | a0001c0001t0020g0283 a0007c0007t0001g0255 |
2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-796+18777T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34273391 | |||||||
| chr19:34273658 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-796+19044T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34273658 | |||||||
| chr19:34273743 | G | A | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-796+19129G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34273743 | |||||||
| chr19:34273937 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(72): Show |
76 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-796+19323C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34273937 | |||||||
| chr19:34274128 | G | A | 3 | a0001c0002t0002g0037 a0001c0002t0002g0038 a0001c0002t0002g0044 |
3 | HG01109.hp2 HG01516.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-796+19514G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34274128 | |||||||
| chr19:34274208 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-796+19594T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34274208 | |||||||
| chr19:34274253 | A | C | 6 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0058 others(3): Show |
6 | HG02258.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-796+19639A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34274253 | |||||||
| chr19:34274337 | G | A | 3 | a0001c0001t0001g0145 a0001c0002t0002g0112 a0001c0002t0002g0133 |
3 | HG03831.hp2 HG04199.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-796+19723G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34274337 | |||||||
| chr19:34274359 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-796+19745C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34274359 | |||||||
| chr19:34274401 | G | A | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-796+19787G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34274401 | |||||||
| chr19:34274417 | A | C | 1 | a0001c0001t0001g0142 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-796+19803A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34274417 | |||||||
| chr19:34274666 | A | G | 5 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0075 others(2): Show |
5 | HG02572.hp1 HG02717.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-796+20052A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34274666 | |||||||
| chr19:34275009 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-796+20395C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34275009 | |||||||
| chr19:34275168 | G | GT | 92 | a0001c0001t0001g0159 a0001c0001t0001g0217 a0001c0001t0001g0233 others(89): Show |
92 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-796+20567dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34275168 | ||||||
| chr19:34275168 | GT | G | 56 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(53): Show |
56 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.-796+20567delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34275168 | ||||||
| chr19:34275261 | C | CAT | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-796+20649_-796+20 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34275261 | ||||||
| chr19:34275504 | G | A | 8 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(5): Show |
8 | NA18950.hp2 NA18965.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.-796+20890G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34275504 | |||||||
| chr19:34275578 | A | G | 1 | a0001c0002t0002g0014 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-796+20964A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34275578 | |||||||
| chr19:34275673 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-796+21059T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34275673 | |||||||
| chr19:34275683 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-796+21069G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34275683 | |||||||
| chr19:34275700 | T | A | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0195 |
3 | HG03453.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-796+21086T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34275700 | |||||||
| chr19:34275912 | T | TC | 4 | a0001c0001t0007g0083 a0001c0001t0007g0084 a0001c0001t0007g0146 others(1): Show |
4 | HG01123.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-796+21300dupC | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34275912 | ||||||
| chr19:34275981 | A | G | 1 | a0001c0001t0007g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-796+21367A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34275981 | |||||||
| chr19:34276022 | G | T | 1 | a0001c0001t0001g0290 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-796+21408G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276022 | |||||||
| chr19:34276193 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-796+21579G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276193 | |||||||
| chr19:34276469 | TTATGTAC others(9): Show |
T | 1 | a0001c0001t0001g0088 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-796+21864_-796+21 others(22): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34276469 | ||||||
| chr19:34276604 | C | G | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-796+21990C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276604 | |||||||
| chr19:34276642 | A | G | 1 | a0001c0001t0001g0321 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-796+22028A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276642 | |||||||
| chr19:34276664 | C | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0126 |
3 | HG01346.hp1 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.-796+22050C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276664 | |||||||
| chr19:34276687 | C | G | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-796+22073C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276687 | |||||||
| chr19:34276688 | C | T | 2 | a0001c0001t0001g0301 a0001c0001t0019g0308 |
2 | HG01081.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-796+22074C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276688 | |||||||
| chr19:34276763 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0195 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-796+22149C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276763 | |||||||
| chr19:34276849 | CTGTGA | C | 6 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0058 others(3): Show |
6 | HG02258.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-796+22236_-796+22 others(11): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276849 | |||||||
| chr19:34276857 | A | C | 6 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0058 others(3): Show |
6 | HG02258.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-796+22243A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276857 | |||||||
| chr19:34276859 | GC | G | 6 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0058 others(3): Show |
6 | HG02258.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-796+22247delC | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34276859 | ||||||
| chr19:34276861 | C | T | 6 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0058 others(3): Show |
6 | HG02258.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-796+22247C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276861 | |||||||
| chr19:34276862 | A | G | 6 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0058 others(3): Show |
6 | HG02258.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-796+22248A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276862 | |||||||
| chr19:34276863 | T | G | 6 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0058 others(3): Show |
6 | HG02258.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-796+22249T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276863 | |||||||
| chr19:34276866 | C | T | 9 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(6): Show |
9 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-796+22252C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276866 | |||||||
| chr19:34276963 | A | T | 1 | a0001c0001t0001g0295 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-796+22349A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276963 | |||||||
| chr19:34276977 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-796+22363C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34276977 | |||||||
| chr19:34277066 | AGT | A | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-796+22453_-796+22 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34277066 | |||||||
| chr19:34277404 | A | T | 19 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(16): Show |
19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-795-22275A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34277404 | |||||||
| chr19:34277425 | T | C | 91 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(88): Show |
91 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-795-22254T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34277425 | |||||||
| chr19:34277449 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-795-22230A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34277449 | |||||||
| chr19:34277685 | C | T | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-21994C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34277685 | |||||||
| chr19:34277726 | C | T | 12 | a0001c0002t0003g0161 a0001c0002t0003g0162 a0001c0002t0003g0163 others(9): Show |
12 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-795-21953C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34277726 | |||||||
| chr19:34277901 | A | AC | 65 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0225 others(62): Show |
65 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.-795-21766dupC | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34277901 | ||||||
| chr19:34277901 | AC | A | 50 | a0001c0001t0001g0144 a0001c0001t0001g0175 a0001c0001t0001g0178 others(47): Show |
50 | HG00140.hp1 HG00280.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.-795-21766delC | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34277901 | ||||||
| chr19:34277901 | ACC | A | 111 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0090 others(108): Show |
111 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-795-21767_-795-21 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34277901 | ||||||
| chr19:34277901 | ACCC | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0085 others(43): Show |
47 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.-795-21768_-795-21 others(9): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34277901 | ||||||
| chr19:34277904 | C | G | 11 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 others(8): Show |
11 | HG00642.hp2 HG00733.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.-795-21775C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34277904 | |||||||
| chr19:34277905 | C | G | 27 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0180 others(24): Show |
27 | HG01074.hp1 HG01081.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.-795-21774C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34277905 | |||||||
| chr19:34277906 | C | T | 3 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 |
3 | HG02055.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-795-21773C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34277906 | |||||||
| chr19:34277913 | C | G | 7 | a0001c0001t0001g0256 a0001c0001t0001g0299 a0001c0001t0001g0305 others(4): Show |
7 | HG00280.hp1 HG01071.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.-795-21766C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34277913 | |||||||
| chr19:34277914 | A | C | 1 | a0001c0001t0001g0253 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-795-21765A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34277914 | |||||||
| chr19:34277994 | C | A | 1 | a0001c0002t0002g0018 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-795-21685C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34277994 | |||||||
| chr19:34278002 | A | T | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-795-21677A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34278002 | |||||||
| chr19:34278347 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-795-21332G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34278347 | |||||||
| chr19:34278351 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(214): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.-795-21328C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34278351 | |||||||
| chr19:34278444 | C | CA | 6 | a0001c0001t0001g0239 a0001c0001t0001g0257 a0001c0001t0001g0303 others(3): Show |
6 | HG01175.hp1 HG01243.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.-795-21212dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34278444 | ||||||
| chr19:34278444 | CA | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.-795-21212delA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34278444 | ||||||
| chr19:34278444 | CAA | C | 13 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(10): Show |
13 | HG00639.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-795-21213_-795-21 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34278444 | ||||||
| chr19:34278678 | T | G | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-795-21001T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34278678 | |||||||
| chr19:34279063 | C | T | 6 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 others(3): Show |
6 | HG02451.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-795-20616C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34279063 | |||||||
| chr19:34279242 | T | C | 2 | a0001c0004t0002g0015 a0001c0004t0002g0033 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-795-20437T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34279242 | |||||||
| chr19:34279369 | G | A | 3 | a0001c0001t0001g0268 a0001c0001t0001g0309 a0001c0001t0001g0310 |
3 | HG00140.hp1 HG01496.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-795-20310G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34279369 | |||||||
| chr19:34279416 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-795-20263C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34279416 | |||||||
| chr19:34279740 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-795-19939C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34279740 | |||||||
| chr19:34279801 | C | T | 22 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 others(19): Show |
22 | HG01099.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-795-19878C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34279801 | |||||||
| chr19:34279842 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-795-19837G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34279842 | |||||||
| chr19:34279971 | C | T | 1 | a0001c0002t0003g0154 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-795-19708C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34279971 | |||||||
| chr19:34279981 | T | C | 1 | a0001c0001t0005g0222 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-795-19698T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34279981 | |||||||
| chr19:34279984 | C | CA | 12 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0254 others(9): Show |
12 | HG00639.hp1 HG01243.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.-795-19672dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34279984 | ||||||
| chr19:34279984 | C | CAA | 32 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(29): Show |
32 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.-795-19673_-795-19 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34279984 | ||||||
| chr19:34279984 | C | CAAA | 6 | a0001c0001t0001g0175 a0001c0001t0001g0185 a0001c0001t0001g0195 others(3): Show |
6 | HG01358.hp2 HG02698.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-795-19674_-795-19 others(9): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34279984 | ||||||
| chr19:34279984 | CA | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0086 others(56): Show |
60 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.-795-19672delA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34279984 | ||||||
| chr19:34279984 | CAA | C | 6 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0075 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-795-19673_-795-19 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34279984 | ||||||
| chr19:34280003 | A | G | 74 | a0001c0001t0001g0159 a0001c0001t0009g0226 a0001c0002t0002g0003 others(71): Show |
74 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-795-19676A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34280003 | |||||||
| chr19:34280331 | T | C | 1 | a0001c0001t0007g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-795-19348T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34280331 | |||||||
| chr19:34280364 | G | A | 4 | a0001c0001t0001g0253 a0001c0001t0001g0260 a0001c0001t0001g0269 others(1): Show |
4 | HG00408.hp2 HG02040.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-795-19315G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34280364 | |||||||
| chr19:34280419 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-795-19260T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34280419 | |||||||
| chr19:34280425 | T | A | 3 | a0001c0002t0002g0027 a0001c0002t0002g0055 a0001c0002t0002g0063 |
3 | NA18943.hp1 NA18945.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-795-19254T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34280425 | |||||||
| chr19:34280526 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-795-19153T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34280526 | |||||||
| chr19:34280560 | T | G | 18 | a0001c0001t0001g0256 a0001c0001t0001g0299 a0001c0001t0001g0300 others(15): Show |
18 | HG00140.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.-795-19119T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34280560 | |||||||
| chr19:34280594 | C | T | 3 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 |
3 | HG02055.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-795-19085C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34280594 | |||||||
| chr19:34280720 | C | G | 3 | a0001c0002t0002g0027 a0001c0002t0002g0055 a0001c0002t0002g0063 |
3 | NA18943.hp1 NA18945.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-795-18959C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34280720 | |||||||
| chr19:34280728 | T | G | 17 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(14): Show |
17 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-795-18951T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34280728 | |||||||
| chr19:34280751 | C | T | 1 | a0001c0012t0001g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-795-18928C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34280751 | |||||||
| chr19:34281435 | C | T | 2 | a0001c0002t0008g0160 a0001c0002t0015g0174 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-795-18244C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34281435 | |||||||
| chr19:34281549 | A | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0234 |
2 | HG02074.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-795-18130A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34281549 | |||||||
| chr19:34281682 | G | A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-17997G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34281682 | |||||||
| chr19:34281725 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-795-17954C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34281725 | |||||||
| chr19:34281752 | CTG | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(57): Show |
61 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.-795-17922_-795-17 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34281752 | ||||||
| chr19:34281923 | C | T | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-795-17756C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34281923 | |||||||
| chr19:34282173 | T | C | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-17506T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34282173 | |||||||
| chr19:34282258 | TCTC | T | 109 | a0001c0001t0001g0159 a0001c0002t0002g0003 a0001c0002t0002g0004 others(106): Show |
109 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.-795-17418_-795-17 others(9): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34282258 | ||||||
| chr19:34282274 | C | T | 2 | a0001c0002t0013g0019 a0001c0002t0013g0020 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-795-17405C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34282274 | |||||||
| chr19:34282277 | G | C | 1 | a0011c0006t0001g0121 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-795-17402G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34282277 | |||||||
| chr19:34282319 | T | C | 18 | a0001c0001t0001g0256 a0001c0001t0001g0299 a0001c0001t0001g0300 others(15): Show |
18 | HG00140.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.-795-17360T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34282319 | |||||||
| chr19:34282580 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-795-17099G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34282580 | |||||||
| chr19:34283046 | A | G | 1 | a0001c0002t0023g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-795-16633A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34283046 | |||||||
| chr19:34283601 | G | T | 3 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 |
3 | HG02055.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-795-16078G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34283601 | |||||||
| chr19:34283663 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0086 others(9): Show |
13 | NA18944.hp1 NA18945.hp2 NA18970.hp1 others(10): Show |
intron_variant | MODIFIER | c.-795-16016C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34283663 | |||||||
| chr19:34283706 | C | G | 1 | a0001c0001t0005g0222 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-795-15973C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34283706 | |||||||
| chr19:34283830 | CT | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(149): Show |
153 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.-795-15830delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34283830 | ||||||
| chr19:34283834 | T | C | 1 | a0001c0001t0007g0146 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-795-15845T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34283834 | |||||||
| chr19:34283893 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-795-15786A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34283893 | |||||||
| chr19:34284031 | C | T | 1 | a0001c0002t0003g0166 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-795-15648C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34284031 | |||||||
| chr19:34284127 | C | CT | 17 | a0001c0001t0001g0216 a0001c0001t0001g0225 a0001c0001t0001g0228 others(14): Show |
17 | HG00621.hp1 HG02027.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.-795-15529dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34284127 | ||||||
| chr19:34284127 | CT | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0081 a0001c0001t0001g0085 others(45): Show |
49 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.-795-15529delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34284127 | ||||||
| chr19:34284127 | CTT | C | 82 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0087 others(79): Show |
82 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.-795-15530_-795-15 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34284127 | ||||||
| chr19:34284127 | CTTT | C | 87 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0181 others(84): Show |
87 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-795-15531_-795-15 others(9): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34284127 | ||||||
| chr19:34284134 | T | C | 10 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(7): Show |
10 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-795-15545T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34284134 | |||||||
| chr19:34284135 | T | C | 2 | a0001c0002t0004g0077 a0001c0002t0010g0029 |
2 | HG02976.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-795-15544T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34284135 | |||||||
| chr19:34284186 | G | A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-15493G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34284186 | |||||||
| chr19:34284548 | T | C | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-15131T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34284548 | |||||||
| chr19:34284710 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-795-14969C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34284710 | |||||||
| chr19:34284816 | A | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.-795-14863A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34284816 | |||||||
| chr19:34284847 | T | C | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-795-14832T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34284847 | |||||||
| chr19:34285093 | C | T | 3 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 |
3 | HG02055.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-795-14586C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34285093 | |||||||
| chr19:34285102 | C | CGT | 4 | a0001c0001t0001g0089 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG00099.hp2 HG00140.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.-795-14562_-795-14 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34285102 | ||||||
| chr19:34285103 | G | A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-14576G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34285103 | |||||||
| chr19:34285319 | C | T | 17 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(14): Show |
17 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-795-14360C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34285319 | |||||||
| chr19:34285339 | C | T | 6 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 others(3): Show |
6 | HG02451.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-795-14340C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34285339 | |||||||
| chr19:34285393 | A | G | 1 | a0001c0001t0001g0324 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-795-14286A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34285393 | |||||||
| chr19:34285547 | C | T | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-795-14132C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34285547 | |||||||
| chr19:34285616 | T | C | 37 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(34): Show |
37 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-795-14063T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34285616 | |||||||
| chr19:34285673 | A | C | 1 | a0001c0001t0001g0298 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-795-14006A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34285673 | |||||||
| chr19:34285674 | C | A | 1 | a0001c0001t0001g0298 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-795-14005C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34285674 | |||||||
| chr19:34285682 | T | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0109 |
2 | HG00609.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.-795-13997T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34285682 | |||||||
| chr19:34285731 | C | T | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-13948C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34285731 | |||||||
| chr19:34285821 | C | G | 1 | a0001c0002t0010g0048 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-795-13858C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34285821 | |||||||
| chr19:34286148 | T | A | 1 | a0001c0002t0002g0057 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-795-13531T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34286148 | |||||||
| chr19:34286220 | GTAT | G | 108 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(105): Show |
108 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-795-13448_-795-13 others(9): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34286220 | ||||||
| chr19:34286242 | C | T | 16 | a0001c0002t0003g0158 a0001c0002t0003g0161 a0001c0002t0003g0162 others(13): Show |
16 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-795-13437C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34286242 | |||||||
| chr19:34286428 | C | T | 4 | a0001c0001t0001g0175 a0001c0001t0001g0192 a0001c0001t0001g0209 others(1): Show |
4 | HG01099.hp2 HG02055.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-795-13251C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34286428 | |||||||
| chr19:34286463 | T | C | 2 | a0001c0002t0013g0019 a0001c0002t0013g0020 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-795-13216T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34286463 | |||||||
| chr19:34286533 | CT | C | 13 | a0001c0001t0001g0089 a0001c0001t0001g0096 a0001c0001t0001g0097 others(10): Show |
13 | HG00099.hp2 HG00140.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-795-13131delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34286533 | ||||||
| chr19:34286565 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-795-13114C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34286565 | |||||||
| chr19:34286592 | A | G | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-13087A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34286592 | |||||||
| chr19:34286658 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-795-13021C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34286658 | |||||||
| chr19:34286661 | C | T | 1 | a0001c0002t0002g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-795-13018C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34286661 | |||||||
| chr19:34286791 | A | G | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-795-12888A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34286791 | |||||||
| chr19:34286939 | T | A | 1 | a0001c0002t0004g0073 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-795-12740T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34286939 | |||||||
| chr19:34287007 | C | T | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-795-12672C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34287007 | |||||||
| chr19:34287011 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-795-12668C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34287011 | |||||||
| chr19:34287038 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-795-12641C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34287038 | |||||||
| chr19:34287056 | G | A | 1 | a0001c0002t0023g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-795-12623G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34287056 | |||||||
| chr19:34287136 | C | CA | 19 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(16): Show |
19 | HG00621.hp1 HG01175.hp2 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.-795-12524dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34287136 | ||||||
| chr19:34287136 | CA | C | 93 | a0001c0001t0001g0135 a0001c0001t0001g0265 a0001c0001t0001g0301 others(90): Show |
93 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-795-12524delA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34287136 | ||||||
| chr19:34287205 | C | T | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-12474C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34287205 | |||||||
| chr19:34288100 | C | T | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-795-11579C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34288100 | |||||||
| chr19:34288235 | T | A | 6 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0058 others(3): Show |
6 | HG02258.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-795-11444T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34288235 | |||||||
| chr19:34288287 | T | A | 1 | a0001c0002t0002g0056 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-795-11392T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34288287 | |||||||
| chr19:34288344 | C | T | 3 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | HG01257.hp1 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-795-11335C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34288344 | |||||||
| chr19:34288610 | G | A | 1 | a0001c0002t0002g0039 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-795-11069G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34288610 | |||||||
| chr19:34288625 | C | T | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-795-11054C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34288625 | |||||||
| chr19:34288652 | C | T | 3 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 |
3 | HG02055.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-795-11027C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34288652 | |||||||
| chr19:34288898 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-795-10781G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34288898 | |||||||
| chr19:34288935 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-795-10744C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34288935 | |||||||
| chr19:34289307 | C | T | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-795-10372C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34289307 | |||||||
| chr19:34289316 | C | A | 1 | a0001c0001t0001g0317 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-795-10363C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34289316 | |||||||
| chr19:34289401 | C | A | 1 | a0001c0002t0002g0017 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-795-10278C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34289401 | |||||||
| chr19:34289522 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-795-10157C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34289522 | |||||||
| chr19:34289669 | C | T | 1 | a0001c0002t0002g0092 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-795-10010C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34289669 | |||||||
| chr19:34289722 | C | CA | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-9946dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34289722 | ||||||
| chr19:34289722 | CA | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0085 others(55): Show |
59 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-795-9946delA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34289722 | ||||||
| chr19:34289728 | A | T | 17 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(14): Show |
17 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-795-9951A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34289728 | |||||||
| chr19:34289733 | A | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0085 others(34): Show |
38 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-9946A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34289733 | |||||||
| chr19:34289735 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-795-9944A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34289735 | |||||||
| chr19:34289876 | C | G | 1 | a0001c0002t0003g0152 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-795-9803C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34289876 | |||||||
| chr19:34289996 | T | C | 1 | a0001c0002t0002g0031 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-795-9683T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34289996 | |||||||
| chr19:34290029 | G | A | 1 | a0001c0002t0002g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-795-9650G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290029 | |||||||
| chr19:34290246 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-795-9433C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290246 | |||||||
| chr19:34290275 | G | A | 2 | a0001c0002t0008g0160 a0001c0002t0015g0174 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-795-9404G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290275 | |||||||
| chr19:34290300 | G | C | 1 | a0001c0002t0002g0125 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-795-9379G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290300 | |||||||
| chr19:34290378 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-795-9301A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290378 | |||||||
| chr19:34290434 | A | G | 5 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0278 others(2): Show |
5 | NA18944.hp2 NA18970.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.-795-9245A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290434 | |||||||
| chr19:34290449 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.-795-9230T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290449 | |||||||
| chr19:34290559 | A | G | 5 | a0001c0001t0001g0245 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
5 | HG02015.hp1 NA18939.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.-795-9120A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290559 | |||||||
| chr19:34290592 | G | C | 73 | a0001c0001t0001g0159 a0001c0002t0002g0003 a0001c0002t0002g0004 others(70): Show |
73 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-795-9087G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290592 | |||||||
| chr19:34290680 | G | T | 73 | a0001c0001t0001g0159 a0001c0002t0002g0003 a0001c0002t0002g0004 others(70): Show |
73 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-795-8999G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290680 | |||||||
| chr19:34290789 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-795-8890A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290789 | |||||||
| chr19:34290833 | A | G | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-795-8846A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290833 | |||||||
| chr19:34290874 | C | CTTTTT | 6 | a0001c0001t0001g0280 a0001c0001t0001g0296 a0001c0001t0001g0297 others(3): Show |
6 | HG02040.hp1 HG02602.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.-795-8759_-795-875 others(9): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0005g0220 a0001c0001t0005g0222 |
2 | NA18960.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-795-8764_-795-875 others(14): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0277 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-795-8765_-795-875 others(15): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTT | C | 8 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0253 others(5): Show |
8 | HG00408.hp2 HG02300.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.-795-8756_-795-875 others(6): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTT | C | 6 | a0001c0001t0001g0206 a0001c0001t0001g0209 a0001c0001t0001g0278 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-795-8757_-795-875 others(7): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTT | C | 11 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 others(8): Show |
11 | HG00733.hp2 HG01099.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-795-8759_-795-875 others(9): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTT | C | 11 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0186 others(8): Show |
11 | HG01175.hp2 HG01358.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-795-8760_-795-875 others(10): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0234 a0001c0001t0001g0290 a0001c0001t0001g0294 others(1): Show |
4 | HG03927.hp1 HG03927.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.-795-8764_-795-875 others(14): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(4): Show |
C | 14 | a0001c0001t0001g0242 a0001c0001t0001g0248 a0001c0001t0001g0249 others(11): Show |
14 | HG00597.hp1 HG01123.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.-795-8765_-795-875 others(15): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(5): Show |
C | 11 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0250 others(8): Show |
11 | HG00609.hp1 HG01943.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.-795-8766_-795-875 others(16): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(6): Show |
C | 8 | a0001c0001t0001g0241 a0001c0001t0001g0244 a0001c0001t0001g0271 others(5): Show |
8 | HG02109.hp1 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-795-8767_-795-875 others(17): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(7): Show |
C | 4 | a0001c0002t0004g0070 a0001c0002t0004g0075 a0001c0002t0004g0077 others(1): Show |
4 | HG02258.hp1 HG02809.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-795-8768_-795-875 others(18): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0270 a0001c0002t0004g0072 |
2 | NA19060.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-795-8769_-795-875 others(19): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0289 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-795-8770_-795-875 others(20): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0292 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-795-8771_-795-875 others(21): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(11): Show |
C | 6 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0103 others(3): Show |
6 | HG01243.hp2 HG01346.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-795-8772_-795-875 others(22): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(12): Show |
C | 30 | a0001c0001t0001g0080 a0001c0001t0001g0086 a0001c0001t0001g0087 others(27): Show |
30 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-795-8773_-795-875 others(23): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(13): Show |
C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0090 others(39): Show |
43 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.-795-8774_-795-875 others(24): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0001g0082 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-795-8775_-795-875 others(25): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(15): Show |
C | 13 | a0001c0002t0002g0006 a0001c0002t0002g0008 a0001c0002t0002g0009 others(10): Show |
13 | HG01123.hp1 HG01256.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-795-8776_-795-875 others(26): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(16): Show |
C | 42 | a0001c0001t0001g0159 a0001c0001t0001g0254 a0001c0001t0001g0282 others(39): Show |
42 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.-795-8777_-795-875 others(27): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(17): Show |
C | 23 | a0001c0001t0001g0317 a0001c0001t0017g0002 a0001c0002t0002g0010 others(20): Show |
23 | HG00639.hp1 HG00733.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-795-8778_-795-875 others(28): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(18): Show |
C | 16 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0158 others(13): Show |
16 | HG00738.hp2 HG01069.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-795-8779_-795-875 others(29): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(19): Show |
C | 1 | a0001c0002t0003g0154 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-795-8780_-795-875 others(30): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(20): Show |
C | 1 | a0001c0001t0001g0314 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-795-8781_-795-875 others(31): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(21): Show |
C | 18 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0256 others(15): Show |
18 | HG00140.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.-795-8782_-795-875 others(32): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(22): Show |
C | 1 | a0001c0001t0001g0311 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-795-8783_-795-875 others(33): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(23): Show |
C | 1 | a0001c0002t0010g0048 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-795-8784_-795-875 others(34): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290874 | CTTTTTTT others(25): Show |
C | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-795-8786_-795-875 others(36): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34290874 | ||||||
| chr19:34290889 | T | C | 1 | a0001c0002t0004g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-795-8790T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290889 | |||||||
| chr19:34290890 | T | C | 1 | a0001c0002t0004g0072 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-795-8789T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290890 | |||||||
| chr19:34290931 | G | T | 1 | a0001c0001t0001g0284 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-795-8748G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290931 | |||||||
| chr19:34290965 | G | A | 2 | a0001c0002t0010g0029 a0001c0002t0010g0048 |
2 | HG00423.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-795-8714G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34290965 | |||||||
| chr19:34291168 | A | G | 12 | a0001c0002t0003g0161 a0001c0002t0003g0162 a0001c0002t0003g0163 others(9): Show |
12 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-795-8511A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34291168 | |||||||
| chr19:34291354 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-795-8325T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34291354 | |||||||
| chr19:34291453 | C | A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-8226C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34291453 | |||||||
| chr19:34291521 | G | A | 17 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(14): Show |
17 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-795-8158G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34291521 | |||||||
| chr19:34291861 | C | CT | 69 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0085 others(66): Show |
70 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.-795-7802dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34291861 | ||||||
| chr19:34291899 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-795-7780G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34291899 | |||||||
| chr19:34292117 | C | T | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-795-7562C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34292117 | |||||||
| chr19:34292196 | C | G | 14 | a0001c0002t0003g0164 a0001c0002t0003g0168 a0001c0002t0003g0170 others(11): Show |
14 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-795-7483C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34292196 | |||||||
| chr19:34292279 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.-795-7400G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34292279 | |||||||
| chr19:34292400 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-795-7279A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34292400 | |||||||
| chr19:34292425 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0282 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-795-7254G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34292425 | |||||||
| chr19:34292587 | T | A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-7092T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34292587 | |||||||
| chr19:34292639 | G | A | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-795-7040G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34292639 | |||||||
| chr19:34292742 | AT | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(203): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-795-6921delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34292742 | ||||||
| chr19:34292811 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-795-6868T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34292811 | |||||||
| chr19:34293023 | A | G | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-795-6656A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293023 | |||||||
| chr19:34293154 | A | G | 1 | a0001c0002t0004g0078 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-795-6525A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293154 | |||||||
| chr19:34293169 | G | T | 16 | a0001c0001t0001g0177 a0001c0001t0001g0182 a0001c0001t0001g0185 others(13): Show |
16 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-795-6510G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293169 | |||||||
| chr19:34293302 | A | G | 1 | a0001c0002t0002g0014 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-795-6377A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293302 | |||||||
| chr19:34293403 | A | AT | 180 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(177): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.-795-6263dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293403 | ||||||
| chr19:34293603 | C | T | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-6076C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293603 | |||||||
| chr19:34293605 | C | T | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-795-6074C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293605 | |||||||
| chr19:34293715 | A | AAAACACA others(21): Show |
1 | a0001c0001t0001g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-795-5963_-795-596 others(32): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293715 | A | AAC | 18 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(15): Show |
18 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-795-5936_-795-593 others(6): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293715 | A | AACAC | 61 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.-795-5938_-795-593 others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293715 | A | AACACAC | 8 | a0001c0002t0002g0022 a0001c0002t0002g0027 a0001c0002t0002g0060 others(5): Show |
8 | HG02486.hp1 HG02717.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.-795-5940_-795-593 others(10): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293715 | A | AACACACA others(3): Show |
5 | a0001c0001t0001g0088 a0001c0001t0001g0098 a0001c0001t0001g0106 others(2): Show |
5 | HG00423.hp2 HG02135.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-795-5944_-795-593 others(14): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293715 | A | AACACACA others(5): Show |
53 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(50): Show |
54 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.-795-5946_-795-593 others(16): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293715 | A | AACACACA others(7): Show |
9 | a0001c0001t0001g0103 a0001c0001t0001g0108 a0001c0001t0001g0113 others(6): Show |
9 | HG01346.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-795-5948_-795-593 others(18): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293715 | A | AACACACA others(9): Show |
8 | a0001c0001t0001g0122 a0001c0001t0001g0135 a0001c0001t0001g0136 others(5): Show |
8 | HG02258.hp1 HG02572.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-795-5950_-795-593 others(20): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293715 | A | AACACACA others(11): Show |
7 | a0001c0001t0001g0081 a0001c0001t0001g0139 a0001c0001t0001g0145 others(4): Show |
7 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-795-5952_-795-593 others(22): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293715 | A | AACACACA others(13): Show |
3 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0003c0005t0012g0319 |
3 | HG02683.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-795-5954_-795-593 others(24): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293715 | A | AACACACA others(15): Show |
1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-795-5956_-795-593 others(26): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293715 | A | AACACACA others(19): Show |
1 | a0001c0001t0001g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-795-5960_-795-593 others(30): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293715 | A | AACACACA others(21): Show |
2 | a0001c0001t0001g0180 a0001c0001t0001g0206 |
2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-795-5962_-795-593 others(32): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293715 | A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0102 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-795-5964_-795-596 others(17): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293715 | |||||||
| chr19:34293715 | A | ACACACAC others(18): Show |
1 | a0004c0010t0001g0189 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-795-5964_-795-596 others(29): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293715 | |||||||
| chr19:34293715 | AAC | A | 100 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0217 others(97): Show |
100 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.-795-5936_-795-593 others(6): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293715 | ||||||
| chr19:34293745 | T | C | 36 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(33): Show |
36 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.-795-5934T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293745 | |||||||
| chr19:34293746 | A | ACACACAC others(2): Show |
11 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0001g0190 others(8): Show |
11 | HG00733.hp2 HG01074.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.-795-5933_-795-593 others(13): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293746 | |||||||
| chr19:34293746 | A | ACACACAC others(4): Show |
4 | a0001c0001t0001g0181 a0001c0001t0001g0196 a0001c0001t0001g0201 others(1): Show |
4 | HG01081.hp2 HG03540.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-795-5933_-795-593 others(15): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293746 | |||||||
| chr19:34293746 | A | ACACACAC others(6): Show |
7 | a0001c0001t0001g0175 a0001c0001t0001g0179 a0001c0001t0001g0187 others(4): Show |
7 | HG01358.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-795-5933_-795-593 others(17): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293746 | |||||||
| chr19:34293746 | A | ACACACAC others(8): Show |
3 | a0001c0001t0001g0184 a0001c0001t0001g0209 a0001c0001t0021g0188 |
3 | HG02055.hp1 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-795-5933_-795-593 others(19): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293746 | |||||||
| chr19:34293746 | A | ACACACAC others(10): Show |
7 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0186 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-795-5933_-795-593 others(21): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293746 | |||||||
| chr19:34293746 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-795-5933A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293746 | |||||||
| chr19:34293747 | T | A | 34 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(31): Show |
34 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.-795-5932T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293747 | |||||||
| chr19:34293747 | T | C | 1 | a0003c0005t0012g0320 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-795-5932T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293747 | |||||||
| chr19:34293748 | T | A | 1 | a0003c0005t0012g0320 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-795-5931T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293748 | |||||||
| chr19:34293748 | T | C | 34 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(31): Show |
34 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.-795-5931T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293748 | |||||||
| chr19:34293749 | T | A | 34 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(31): Show |
34 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.-795-5930T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293749 | |||||||
| chr19:34293750 | C | A | 1 | a0003c0005t0012g0320 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-795-5929C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293750 | |||||||
| chr19:34293750 | C | CT | 57 | a0001c0001t0001g0001 a0001c0001t0001g0086 a0001c0001t0001g0088 others(54): Show |
58 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.-795-5903dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293750 | ||||||
| chr19:34293750 | C | CTT | 17 | a0001c0001t0001g0085 a0001c0001t0001g0093 a0001c0001t0001g0094 others(14): Show |
17 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.-795-5904_-795-590 others(6): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293750 | ||||||
| chr19:34293750 | CT | C | 75 | a0001c0001t0001g0081 a0001c0001t0001g0134 a0001c0001t0001g0137 others(72): Show |
75 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-795-5903delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34293750 | ||||||
| chr19:34293751 | T | A | 34 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(31): Show |
34 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.-795-5928T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293751 | |||||||
| chr19:34293751 | T | C | 1 | a0001c0002t0002g0063 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-795-5928T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293751 | |||||||
| chr19:34293752 | T | A | 1 | a0001c0002t0002g0063 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-795-5927T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293752 | |||||||
| chr19:34293752 | T | C | 34 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(31): Show |
34 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.-795-5927T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293752 | |||||||
| chr19:34293753 | T | A | 34 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(31): Show |
34 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.-795-5926T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293753 | |||||||
| chr19:34293754 | T | A | 1 | a0001c0002t0002g0063 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-795-5925T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293754 | |||||||
| chr19:34293754 | T | C | 1 | a0003c0005t0012g0320 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-795-5925T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293754 | |||||||
| chr19:34293755 | T | A | 34 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(31): Show |
34 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.-795-5924T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293755 | |||||||
| chr19:34293758 | T | C | 1 | a0001c0002t0002g0063 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-795-5921T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293758 | |||||||
| chr19:34293759 | T | C | 34 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(31): Show |
34 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.-795-5920T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293759 | |||||||
| chr19:34293818 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-795-5861G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293818 | |||||||
| chr19:34293820 | G | A | 1 | a0001c0002t0009g0230 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-795-5859G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34293820 | |||||||
| chr19:34294226 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-795-5453C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34294226 | |||||||
| chr19:34294227 | G | A | 16 | a0001c0002t0003g0158 a0001c0002t0003g0161 a0001c0002t0003g0162 others(13): Show |
16 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-795-5452G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34294227 | |||||||
| chr19:34294256 | CA | C | 7 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0075 others(4): Show |
7 | HG02572.hp1 HG02683.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-795-5410delA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34294256 | ||||||
| chr19:34294348 | A | G | 5 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0278 others(2): Show |
5 | NA18944.hp2 NA18970.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.-795-5331A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34294348 | |||||||
| chr19:34294452 | TAAA | T | 6 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(3): Show |
6 | HG00642.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-795-5223_-795-522 others(7): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34294452 | ||||||
| chr19:34294518 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-795-5161C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34294518 | |||||||
| chr19:34294629 | G | GT | 170 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(167): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-795-5044dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34294629 | ||||||
| chr19:34294729 | G | A | 3 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 |
3 | HG02055.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-795-4950G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34294729 | |||||||
| chr19:34294744 | G | A | 4 | a0001c0001t0007g0083 a0001c0001t0007g0084 a0001c0001t0007g0146 others(1): Show |
4 | HG01123.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-795-4935G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34294744 | |||||||
| chr19:34294817 | G | T | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-795-4862G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34294817 | |||||||
| chr19:34294833 | C | T | 1 | a0001c0002t0004g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-795-4846C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34294833 | |||||||
| chr19:34295045 | C | T | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-795-4634C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34295045 | |||||||
| chr19:34295105 | C | A | 93 | a0001c0001t0001g0159 a0001c0002t0002g0003 a0001c0002t0002g0004 others(90): Show |
93 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-795-4574C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34295105 | |||||||
| chr19:34295230 | A | G | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-4449A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34295230 | |||||||
| chr19:34295231 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-795-4448T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34295231 | |||||||
| chr19:34295515 | G | GTGTTT | 78 | a0001c0001t0001g0159 a0001c0002t0002g0003 a0001c0002t0002g0004 others(75): Show |
78 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-795-4137_-795-413 others(9): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34295515 | ||||||
| chr19:34295515 | G | GTGTTTTG others(3): Show |
11 | a0001c0001t0007g0083 a0001c0001t0007g0084 a0001c0001t0007g0146 others(8): Show |
11 | HG01123.hp2 HG01168.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.-795-4142_-795-413 others(14): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34295515 | ||||||
| chr19:34295515 | G | GTGTTTTG others(8): Show |
17 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(14): Show |
17 | HG02451.hp2 HG02717.hp2 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.-795-4147_-795-413 others(19): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34295515 | ||||||
| chr19:34295515 | G | GTGTTTTG others(13): Show |
17 | a0001c0002t0003g0152 a0001c0002t0003g0158 a0001c0002t0003g0161 others(14): Show |
17 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-795-4152_-795-413 others(24): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34295515 | ||||||
| chr19:34295515 | G | GTGTTTTG others(18): Show |
2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-795-4157_-795-413 others(29): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34295515 | ||||||
| chr19:34295515 | GTGTTTTG others(3): Show |
G | 1 | a0001c0001t0001g0107 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-795-4142_-795-413 others(14): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34295515 | ||||||
| chr19:34295705 | AT | A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-3968delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34295705 | ||||||
| chr19:34295742 | A | T | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-795-3937A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34295742 | |||||||
| chr19:34295773 | C | T | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-795-3906C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34295773 | |||||||
| chr19:34295929 | C | G | 1 | a0001c0001t0009g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-795-3750C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34295929 | |||||||
| chr19:34296152 | C | CTT | 20 | a0001c0001t0001g0159 a0001c0001t0001g0209 a0001c0001t0001g0210 others(17): Show |
20 | HG00280.hp2 HG01099.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-795-3517_-795-351 others(6): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34296152 | ||||||
| chr19:34296200 | A | T | 4 | a0001c0001t0001g0217 a0001c0001t0001g0234 a0001c0001t0001g0244 others(1): Show |
4 | HG02074.hp2 HG02129.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.-795-3479A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34296200 | |||||||
| chr19:34296220 | G | A | 17 | a0001c0001t0001g0228 a0001c0001t0001g0235 a0001c0001t0001g0237 others(14): Show |
17 | HG00621.hp1 HG01891.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.-795-3459G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34296220 | |||||||
| chr19:34296239 | G | C | 41 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(38): Show |
41 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.-795-3440G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34296239 | |||||||
| chr19:34296288 | C | T | 19 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(16): Show |
19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-795-3391C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34296288 | |||||||
| chr19:34296293 | T | A | 2 | a0001c0001t0001g0301 a0001c0001t0019g0308 |
2 | HG01081.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-795-3386T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34296293 | |||||||
| chr19:34296542 | G | A | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-795-3137G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34296542 | |||||||
| chr19:34296875 | C | T | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-795-2804C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34296875 | |||||||
| chr19:34297010 | G | A | 4 | a0001c0001t0007g0083 a0001c0001t0007g0084 a0001c0001t0007g0146 others(1): Show |
4 | HG01123.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-795-2669G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34297010 | |||||||
| chr19:34297025 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-795-2654G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34297025 | |||||||
| chr19:34297078 | G | C | 2 | a0001c0002t0002g0013 a0001c0002t0002g0041 |
2 | NA18982.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-795-2601G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34297078 | |||||||
| chr19:34297246 | C | G | 1 | a0001c0001t0001g0298 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-795-2433C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34297246 | |||||||
| chr19:34297306 | A | G | 74 | a0001c0001t0001g0159 a0001c0002t0002g0003 a0001c0002t0002g0004 others(71): Show |
74 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-795-2373A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34297306 | |||||||
| chr19:34297403 | GA | G | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-795-2271delA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34297403 | ||||||
| chr19:34297551 | A | T | 1 | a0001c0002t0004g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-795-2128A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34297551 | |||||||
| chr19:34297650 | C | T | 1 | a0001c0002t0003g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-795-2029C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34297650 | |||||||
| chr19:34298103 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(168): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-795-1576A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34298103 | |||||||
| chr19:34298144 | C | T | 1 | a0001c0002t0025g0035 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-795-1535C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34298144 | |||||||
| chr19:34298245 | G | A | 3 | a0001c0001t0001g0253 a0001c0001t0001g0260 a0001c0001t0001g0280 |
3 | HG00408.hp2 HG02040.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-795-1434G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34298245 | |||||||
| chr19:34298277 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-795-1402A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34298277 | |||||||
| chr19:34298397 | C | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-795-1282C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34298397 | |||||||
| chr19:34298413 | C | CA | 40 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(37): Show |
40 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.-795-1252dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34298413 | ||||||
| chr19:34298499 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-795-1180G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34298499 | |||||||
| chr19:34298583 | G | A | 1 | a0001c0001t0022g0147 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-795-1096G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34298583 | |||||||
| chr19:34298713 | AAAT | A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-795-954_-795-952d others(5): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 34298713 | ||||||
| chr19:34298716 | T | A | 1 | a0001c0001t0001g0315 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-795-963T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34298716 | |||||||
| chr19:34298762 | C | T | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-795-917C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34298762 | |||||||
| chr19:34298849 | C | T | 41 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(38): Show |
41 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.-795-830C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34298849 | |||||||
| chr19:34298973 | G | A | 1 | a0001c0002t0002g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-795-706G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34298973 | |||||||
| chr19:34299074 | C | T | 7 | a0001c0001t0001g0081 a0001c0001t0001g0139 a0001c0001t0001g0140 others(4): Show |
7 | HG02886.hp1 HG02976.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-795-605C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34299074 | |||||||
| chr19:34299237 | A | T | 2 | a0001c0002t0003g0153 a0001c0002t0003g0154 |
2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-795-442A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34299237 | |||||||
| chr19:34299311 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-795-368G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34299311 | |||||||
| chr19:34299383 | A | C | 2 | a0001c0002t0004g0073 a0001c0002t0004g0074 |
2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-795-296A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34299383 | |||||||
| chr19:34299608 | T | A | 1 | a0001c0001t0001g0286 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-795-71T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 1/13 | chr19 | 34299608 | |||||||
| chr19:34301214 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.495+246G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34301214 | |||||||
| chr19:34301428 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.495+460T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34301428 | |||||||
| chr19:34301462 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.495+494C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34301462 | |||||||
| chr19:34301494 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.495+526G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34301494 | |||||||
| chr19:34301513 | C | CA | 24 | a0001c0001t0001g0217 a0001c0001t0001g0225 a0001c0001t0001g0231 others(21): Show |
24 | HG01175.hp1 HG01358.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.495+570dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34301513 | ||||||
| chr19:34301513 | CA | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0088 others(46): Show |
50 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.495+570delA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34301513 | ||||||
| chr19:34301513 | CAA | C | 121 | a0001c0001t0001g0080 a0001c0001t0001g0136 a0001c0001t0001g0137 others(118): Show |
121 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.495+569_495+570del others(2): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34301513 | ||||||
| chr19:34301513 | CAAAAAAA others(2): Show |
C | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.495+562_495+570del others(9): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34301513 | ||||||
| chr19:34301531 | A | G | 19 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(16): Show |
19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.495+563A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34301531 | |||||||
| chr19:34301533 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.495+565A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34301533 | |||||||
| chr19:34301535 | A | G | 92 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(89): Show |
92 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.495+567A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34301535 | |||||||
| chr19:34301589 | T | A | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.495+621T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34301589 | |||||||
| chr19:34301684 | A | AT | 19 | a0001c0001t0001g0116 a0001c0001t0001g0145 a0001c0001t0001g0185 others(16): Show |
19 | HG01175.hp2 HG01358.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.495+732dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34301684 | ||||||
| chr19:34301684 | AT | A | 6 | a0001c0001t0007g0083 a0001c0001t0007g0084 a0001c0001t0007g0146 others(3): Show |
6 | HG01123.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+732delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34301684 | ||||||
| chr19:34301961 | G | T | 1 | a0011c0006t0001g0121 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.495+993G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34301961 | |||||||
| chr19:34301975 | G | A | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.495+1007G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34301975 | |||||||
| chr19:34301982 | C | CT | 26 | a0001c0001t0001g0175 a0001c0001t0001g0195 a0001c0001t0001g0199 others(23): Show |
26 | HG00597.hp1 HG00639.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.495+1041dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34301982 | ||||||
| chr19:34301982 | C | CTT | 57 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0009 others(54): Show |
57 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.495+1040_495+1041d others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34301982 | ||||||
| chr19:34301982 | C | CTTT | 11 | a0001c0002t0002g0008 a0001c0002t0002g0024 a0001c0002t0002g0046 others(8): Show |
11 | HG00423.hp1 HG01099.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.495+1039_495+1041d others(5): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34301982 | ||||||
| chr19:34301982 | CT | C | 25 | a0001c0001t0001g0086 a0001c0001t0001g0094 a0001c0001t0001g0099 others(22): Show |
25 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.495+1041delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34301982 | ||||||
| chr19:34301982 | CTT | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(80): Show |
84 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.495+1040_495+1041d others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34301982 | ||||||
| chr19:34301982 | CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0001g0081 a0001c0001t0001g0137 a0001c0001t0001g0139 others(5): Show |
8 | HG02886.hp1 HG02976.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+1034_495+1041d others(10): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34301982 | ||||||
| chr19:34302020 | C | T | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.495+1052C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302020 | |||||||
| chr19:34302139 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.495+1171C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302139 | |||||||
| chr19:34302140 | G | A | 19 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(16): Show |
19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.495+1172G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302140 | |||||||
| chr19:34302171 | G | A | 1 | a0001c0002t0003g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.495+1203G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302171 | |||||||
| chr19:34302257 | G | T | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.495+1289G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302257 | |||||||
| chr19:34302276 | G | T | 2 | a0001c0002t0008g0160 a0001c0002t0015g0174 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.495+1308G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302276 | |||||||
| chr19:34302292 | G | GT | 194 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(191): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.495+1344dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34302292 | ||||||
| chr19:34302292 | G | GTT | 66 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(63): Show |
66 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.495+1343_495+1344d others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34302292 | ||||||
| chr19:34302292 | G | GTTT | 9 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0001g0145 others(6): Show |
9 | HG02109.hp1 HG02572.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.495+1342_495+1344d others(5): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34302292 | ||||||
| chr19:34302311 | T | TC | 3 | a0001c0002t0002g0060 a0001c0002t0002g0062 a0001c0002t0009g0230 |
3 | NA18747.hp1 NA18940.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.495+1343_495+1344i others(3): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302311 | |||||||
| chr19:34302316 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.495+1348A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302316 | |||||||
| chr19:34302369 | A | C | 7 | a0001c0001t0001g0081 a0001c0001t0001g0139 a0001c0001t0001g0140 others(4): Show |
7 | HG02886.hp1 HG02976.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+1401A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302369 | |||||||
| chr19:34302507 | C | T | 1 | a0003c0005t0012g0319 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.495+1539C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302507 | |||||||
| chr19:34302717 | T | C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | NA18986.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.495+1749T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302717 | |||||||
| chr19:34302736 | G | GT | 10 | a0001c0001t0001g0199 a0001c0001t0001g0209 a0001c0001t0001g0216 others(7): Show |
10 | HG01175.hp2 HG01358.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.495+1792dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34302736 | ||||||
| chr19:34302736 | GT | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0085 others(74): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.495+1792delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34302736 | ||||||
| chr19:34302736 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0001g0298 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.495+1783_495+1792d others(12): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34302736 | ||||||
| chr19:34302741 | T | G | 90 | a0001c0001t0001g0159 a0001c0001t0001g0193 a0001c0001t0009g0226 others(87): Show |
90 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.495+1773T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302741 | |||||||
| chr19:34302742 | T | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0085 others(64): Show |
68 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.495+1774T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302742 | |||||||
| chr19:34302743 | T | G | 2 | a0001c0001t0001g0109 a0001c0002t0004g0077 |
2 | HG02015.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.495+1775T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302743 | |||||||
| chr19:34302744 | T | A | 1 | a0001c0001t0007g0146 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.495+1776T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302744 | |||||||
| chr19:34302801 | G | A | 316 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(313): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.495+1833G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302801 | |||||||
| chr19:34302944 | C | T | 1 | a0001c0002t0002g0173 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.495+1976C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34302944 | |||||||
| chr19:34303057 | A | T | 1 | a0001c0002t0002g0008 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.495+2089A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34303057 | |||||||
| chr19:34303090 | T | G | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.495+2122T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34303090 | |||||||
| chr19:34303290 | G | T | 1 | a0001c0002t0003g0165 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.495+2322G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34303290 | |||||||
| chr19:34303368 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.495+2400G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34303368 | |||||||
| chr19:34303495 | G | A | 2 | a0001c0001t0001g0301 a0001c0001t0019g0308 |
2 | HG01081.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.495+2527G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34303495 | |||||||
| chr19:34303685 | G | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0218 |
2 | HG02647.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.495+2717G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34303685 | |||||||
| chr19:34303808 | G | T | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.495+2840G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34303808 | |||||||
| chr19:34303837 | A | G | 2 | a0001c0002t0008g0160 a0001c0002t0015g0174 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.495+2869A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34303837 | |||||||
| chr19:34303841 | C | T | 19 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(16): Show |
19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.495+2873C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34303841 | |||||||
| chr19:34303896 | T | G | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.495+2928T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34303896 | |||||||
| chr19:34304016 | C | T | 6 | a0001c0001t0001g0228 a0001c0001t0001g0243 a0001c0001t0001g0246 others(3): Show |
6 | HG00621.hp1 NA18747.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+3048C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34304016 | |||||||
| chr19:34304096 | AT | A | 161 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0136 others(158): Show |
161 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.495+3143delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34304096 | ||||||
| chr19:34304098 | T | A | 42 | a0001c0001t0001g0159 a0001c0002t0002g0003 a0001c0002t0002g0004 others(39): Show |
42 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.495+3130T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34304098 | |||||||
| chr19:34304099 | T | A | 1 | a0001c0002t0002g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.495+3131T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34304099 | |||||||
| chr19:34304101 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0085 others(51): Show |
55 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.495+3133T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34304101 | |||||||
| chr19:34304324 | CAAA | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(56): Show |
60 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.495+3358_495+3360d others(5): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34304324 | ||||||
| chr19:34304345 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.495+3377G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34304345 | |||||||
| chr19:34304374 | A | AT | 41 | a0001c0001t0001g0080 a0001c0001t0001g0116 a0001c0001t0001g0218 others(38): Show |
41 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.495+3425dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34304374 | ||||||
| chr19:34304374 | AT | A | 9 | a0001c0001t0001g0087 a0001c0001t0001g0113 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp1 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.495+3425delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34304374 | ||||||
| chr19:34304523 | G | A | 4 | a0001c0002t0002g0009 a0001c0002t0002g0032 a0003c0005t0012g0319 others(1): Show |
4 | HG01169.hp2 HG02148.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+3555G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34304523 | |||||||
| chr19:34304574 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(56): Show |
60 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.495+3606C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34304574 | |||||||
| chr19:34304741 | AGT | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0130 |
3 | NA18944.hp1 NA19065.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.495+3778_495+3779d others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34304741 | ||||||
| chr19:34304860 | C | T | 73 | a0001c0001t0009g0226 a0001c0002t0002g0003 a0001c0002t0002g0004 others(70): Show |
73 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.495+3892C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34304860 | |||||||
| chr19:34304948 | C | T | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.495+3980C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34304948 | |||||||
| chr19:34305001 | C | A | 72 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(69): Show |
72 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.495+4033C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305001 | |||||||
| chr19:34305027 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.495+4059C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305027 | |||||||
| chr19:34305044 | G | A | 35 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(32): Show |
35 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.495+4076G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305044 | |||||||
| chr19:34305066 | A | G | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0195 |
3 | HG03453.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.495+4098A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305066 | |||||||
| chr19:34305089 | G | C | 1 | a0001c0002t0002g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.495+4121G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305089 | |||||||
| chr19:34305103 | A | G | 1 | a0001c0001t0001g0325 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.495+4135A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305103 | |||||||
| chr19:34305107 | T | G | 1 | a0001c0012t0001g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.495+4139T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305107 | |||||||
| chr19:34305128 | A | G | 1 | a0001c0012t0001g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.495+4160A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305128 | |||||||
| chr19:34305262 | A | C | 1 | a0001c0001t0001g0325 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.495+4294A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305262 | |||||||
| chr19:34305329 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.495+4361A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305329 | |||||||
| chr19:34305390 | T | C | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.495+4422T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305390 | |||||||
| chr19:34305426 | A | T | 2 | a0001c0002t0008g0160 a0001c0002t0015g0174 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.495+4458A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305426 | |||||||
| chr19:34305450 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.495+4482C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305450 | |||||||
| chr19:34305538 | C | G | 74 | a0001c0001t0009g0226 a0001c0002t0002g0003 a0001c0002t0002g0004 others(71): Show |
74 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.495+4570C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305538 | |||||||
| chr19:34305905 | T | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(257): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.495+4937T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305905 | |||||||
| chr19:34305929 | G | A | 10 | a0001c0001t0001g0081 a0001c0001t0001g0106 a0001c0001t0001g0136 others(7): Show |
10 | HG00423.hp2 HG02886.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.495+4961G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34305929 | |||||||
| chr19:34306115 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.495+5147A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34306115 | |||||||
| chr19:34306517 | T | A | 3 | a0002c0003t0003g0155 a0002c0003t0003g0156 a0002c0003t0003g0157 |
3 | HG01168.hp1 HG01169.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.495+5549T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34306517 | |||||||
| chr19:34306870 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.495+5902T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34306870 | |||||||
| chr19:34306924 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(53): Show |
57 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.495+5956G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34306924 | |||||||
| chr19:34306976 | G | A | 1 | a0001c0001t0001g0323 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.495+6008G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34306976 | |||||||
| chr19:34307130 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.495+6162G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307130 | |||||||
| chr19:34307175 | G | A | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.495+6207G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307175 | |||||||
| chr19:34307263 | T | A | 2 | a0001c0002t0002g0009 a0001c0002t0002g0032 |
2 | HG01169.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.495+6295T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307263 | |||||||
| chr19:34307298 | T | G | 1 | a0001c0001t0001g0273 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.495+6330T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307298 | |||||||
| chr19:34307299 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.495+6331T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307299 | |||||||
| chr19:34307436 | T | C | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.495+6468T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307436 | |||||||
| chr19:34307537 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.495+6569T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307537 | |||||||
| chr19:34307590 | T | C | 1 | a0001c0002t0015g0174 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.495+6622T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307590 | |||||||
| chr19:34307598 | C | G | 1 | a0001c0002t0004g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.495+6630C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307598 | |||||||
| chr19:34307648 | C | CATACTTA others(29): Show |
1 | a0003c0005t0012g0320 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.495+6712_495+6747d others(38): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34307648 | ||||||
| chr19:34307648 | C | CATACTTA others(47): Show |
1 | a0003c0005t0012g0319 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.495+6694_495+6747d others(56): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34307648 | ||||||
| chr19:34307648 | CATACTTA others(11): Show |
C | 42 | a0001c0001t0001g0080 a0001c0001t0001g0111 a0001c0001t0001g0215 others(39): Show |
42 | HG00621.hp1 HG01891.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.495+6730_495+6747d others(20): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34307648 | ||||||
| chr19:34307648 | CATACTTA others(29): Show |
C | 88 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(85): Show |
88 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.495+6712_495+6747d others(38): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34307648 | ||||||
| chr19:34307674 | TATATAC | T | 3 | a0001c0002t0002g0008 a0001c0002t0002g0042 a0001c0002t0024g0043 |
3 | HG00280.hp2 HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.495+6712_495+6717d others(8): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34307674 | ||||||
| chr19:34307675 | A | G | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.495+6707A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307675 | |||||||
| chr19:34307688 | CT | C | 3 | a0001c0002t0002g0008 a0001c0002t0002g0042 a0001c0002t0024g0043 |
3 | HG00280.hp2 HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.495+6722delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34307688 | ||||||
| chr19:34307707 | TTA | T | 3 | a0001c0002t0002g0008 a0001c0002t0002g0042 a0001c0002t0024g0043 |
3 | HG00280.hp2 HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.495+6748_495+6749d others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34307707 | ||||||
| chr19:34307735 | C | G | 3 | a0001c0002t0002g0008 a0001c0002t0002g0042 a0001c0002t0024g0043 |
3 | HG00280.hp2 HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.495+6767C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307735 | |||||||
| chr19:34307736 | T | TA | 3 | a0001c0002t0002g0008 a0001c0002t0002g0042 a0001c0002t0024g0043 |
3 | HG00280.hp2 HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.495+6768_495+6769i others(3): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307736 | |||||||
| chr19:34307745 | C | CTATAAAA | 3 | a0001c0002t0002g0008 a0001c0002t0002g0042 a0001c0002t0024g0043 |
3 | HG00280.hp2 HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.495+6781_495+6782i others(9): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34307745 | ||||||
| chr19:34307792 | TA | T | 44 | a0001c0001t0001g0144 a0001c0001t0001g0175 a0001c0001t0001g0176 others(41): Show |
44 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.495+6834delA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34307792 | ||||||
| chr19:34307792 | TAA | T | 32 | a0001c0001t0009g0226 a0001c0001t0022g0147 a0001c0002t0002g0010 others(29): Show |
32 | HG00423.hp1 HG00733.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.495+6833_495+6834d others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34307792 | ||||||
| chr19:34307793 | A | T | 4 | a0001c0001t0001g0227 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
4 | NA18962.hp1 NA18965.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+6825A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307793 | |||||||
| chr19:34307797 | A | T | 2 | a0001c0002t0004g0073 a0001c0002t0004g0074 |
2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.495+6829A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307797 | |||||||
| chr19:34307799 | A | AT | 4 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+6831_495+6832i others(3): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307799 | |||||||
| chr19:34307799 | A | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.495+6831A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307799 | |||||||
| chr19:34307801 | A | AAT | 14 | a0001c0002t0003g0161 a0001c0002t0003g0162 a0001c0002t0003g0163 others(11): Show |
14 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.495+6846_495+6847d others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34307801 | ||||||
| chr19:34307801 | A | AT | 4 | a0001c0001t0001g0142 a0001c0001t0001g0254 a0001c0001t0020g0283 others(1): Show |
4 | HG02300.hp1 HG02486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+6833_495+6834i others(3): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307801 | |||||||
| chr19:34307801 | A | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.495+6833A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307801 | |||||||
| chr19:34307814 | A | AT | 24 | a0001c0001t0001g0215 a0001c0001t0001g0228 a0001c0001t0001g0235 others(21): Show |
24 | HG00621.hp1 HG01891.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.495+6861dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34307814 | ||||||
| chr19:34307815 | T | TA | 7 | a0001c0001t0001g0085 a0001c0001t0001g0231 a0001c0001t0001g0232 others(4): Show |
7 | HG02074.hp1 HG02965.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+6847_495+6848i others(3): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307815 | |||||||
| chr19:34307816 | T | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.495+6848T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307816 | |||||||
| chr19:34307817 | T | A | 2 | a0001c0001t0001g0085 a0001c0001t0007g0083 |
2 | HG02074.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.495+6849T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307817 | |||||||
| chr19:34307818 | T | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0081 a0001c0001t0001g0082 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.495+6850T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307818 | |||||||
| chr19:34307819 | T | A | 1 | a0001c0001t0001g0085 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.495+6851T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307819 | |||||||
| chr19:34307820 | T | A | 56 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0175 others(53): Show |
56 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.495+6852T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307820 | |||||||
| chr19:34307822 | T | A | 1 | a0001c0002t0003g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.495+6854T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307822 | |||||||
| chr19:34307839 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.495+6871G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307839 | |||||||
| chr19:34307912 | T | G | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.495+6944T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307912 | |||||||
| chr19:34307916 | A | C | 1 | a0001c0001t0017g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.495+6948A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34307916 | |||||||
| chr19:34308238 | C | CT | 19 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0001c0001t0001g0244 others(16): Show |
19 | HG00140.hp1 HG01261.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.495+7292dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34308238 | ||||||
| chr19:34308238 | CT | C | 15 | a0001c0001t0001g0215 a0001c0001t0001g0299 a0001c0001t0001g0302 others(12): Show |
15 | HG01069.hp2 HG01256.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.495+7292delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34308238 | ||||||
| chr19:34308260 | T | C | 1 | a0001c0002t0002g0011 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.495+7292T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34308260 | |||||||
| chr19:34308391 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.495+7423G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34308391 | |||||||
| chr19:34308524 | A | C | 103 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0136 others(100): Show |
103 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.495+7556A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34308524 | |||||||
| chr19:34309025 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0134 |
2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.495+8057G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309025 | |||||||
| chr19:34309049 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.495+8081T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309049 | |||||||
| chr19:34309064 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.495+8096A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309064 | |||||||
| chr19:34309077 | T | TA | 38 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(35): Show |
38 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.495+8120dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34309077 | ||||||
| chr19:34309078 | A | T | 6 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0075 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.495+8110A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309078 | |||||||
| chr19:34309158 | C | T | 2 | a0001c0002t0002g0092 a0001c0002t0002g0132 |
2 | NA18960.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.495+8190C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309158 | |||||||
| chr19:34309178 | G | A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.495+8210G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309178 | |||||||
| chr19:34309185 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0275 |
2 | HG02129.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.495+8217C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309185 | |||||||
| chr19:34309399 | C | T | 1 | a0001c0002t0003g0152 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.495+8431C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309399 | |||||||
| chr19:34309400 | A | G | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.495+8432A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309400 | |||||||
| chr19:34309401 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.495+8433T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309401 | |||||||
| chr19:34309638 | C | A | 1 | a0001c0002t0014g0071 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.495+8670C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309638 | |||||||
| chr19:34309651 | G | A | 1 | a0001c0012t0001g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.495+8683G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309651 | |||||||
| chr19:34309693 | G | A | 39 | a0001c0001t0001g0122 a0001c0001t0001g0175 a0001c0001t0001g0176 others(36): Show |
39 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.495+8725G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309693 | |||||||
| chr19:34309699 | G | A | 1 | a0004c0010t0001g0189 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.495+8731G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309699 | |||||||
| chr19:34309844 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.495+8876A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309844 | |||||||
| chr19:34309859 | G | A | 2 | a0001c0002t0004g0070 a0001c0002t0004g0072 |
2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.495+8891G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34309859 | |||||||
| chr19:34310538 | C | G | 109 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(106): Show |
109 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.496-9369C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34310538 | |||||||
| chr19:34310633 | CAT | C | 3 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | HG01257.hp1 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.496-9273_496-9272d others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34310633 | |||||||
| chr19:34310776 | G | A | 1 | a0001c0002t0002g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.496-9131G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34310776 | |||||||
| chr19:34310997 | C | A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.496-8910C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34310997 | |||||||
| chr19:34311002 | G | GC | 16 | a0001c0001t0001g0108 a0001c0001t0001g0116 a0001c0001t0001g0209 others(13): Show |
16 | HG01074.hp2 HG01099.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.496-8898dupC | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34311002 | ||||||
| chr19:34311206 | G | A | 2 | a0001c0002t0002g0064 a0001c0002t0002g0065 |
2 | HG01346.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.496-8701G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34311206 | |||||||
| chr19:34311374 | G | A | 1 | a0001c0002t0004g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.496-8533G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34311374 | |||||||
| chr19:34311409 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.496-8498C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34311409 | |||||||
| chr19:34311475 | A | T | 1 | a0001c0001t0001g0234 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.496-8432A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34311475 | |||||||
| chr19:34311485 | C | G | 3 | a0002c0003t0003g0155 a0002c0003t0003g0156 a0002c0003t0003g0157 |
3 | HG01168.hp1 HG01169.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.496-8422C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34311485 | |||||||
| chr19:34311488 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.496-8419A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34311488 | |||||||
| chr19:34311626 | C | G | 1 | a0001c0001t0001g0228 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.496-8281C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34311626 | |||||||
| chr19:34311907 | G | A | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.496-8000G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34311907 | |||||||
| chr19:34312254 | C | G | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.496-7653C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34312254 | |||||||
| chr19:34312286 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(57): Show |
61 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.496-7621G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34312286 | |||||||
| chr19:34312302 | A | T | 2 | a0001c0001t0001g0285 a0001c0001t0017g0002 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.496-7605A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34312302 | |||||||
| chr19:34312436 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(53): Show |
57 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.496-7471A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34312436 | |||||||
| chr19:34312450 | G | A | 1 | a0008c0008t0001g0318 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.496-7457G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34312450 | |||||||
| chr19:34312524 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.496-7383G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34312524 | |||||||
| chr19:34312772 | C | T | 1 | a0001c0002t0023g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.496-7135C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34312772 | |||||||
| chr19:34312974 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.496-6933T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34312974 | |||||||
| chr19:34313263 | C | A | 2 | a0001c0002t0008g0160 a0001c0002t0015g0174 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.496-6644C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34313263 | |||||||
| chr19:34313286 | G | A | 3 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0006c0014t0001g0304 |
3 | HG01069.hp2 HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.496-6621G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34313286 | |||||||
| chr19:34313515 | G | C | 40 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(37): Show |
40 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.496-6392G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34313515 | |||||||
| chr19:34313530 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.496-6377G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34313530 | |||||||
| chr19:34313768 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.496-6139A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34313768 | |||||||
| chr19:34313985 | G | C | 91 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(88): Show |
91 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.496-5922G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34313985 | |||||||
| chr19:34314070 | G | A | 72 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(69): Show |
72 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.496-5837G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34314070 | |||||||
| chr19:34314342 | T | C | 2 | a0001c0002t0003g0153 a0001c0002t0003g0154 |
2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.496-5565T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34314342 | |||||||
| chr19:34314367 | G | T | 5 | a0001c0001t0001g0245 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
5 | HG02015.hp1 NA18939.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.496-5540G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34314367 | |||||||
| chr19:34314389 | T | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.496-5518T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34314389 | |||||||
| chr19:34314545 | A | G | 91 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(88): Show |
91 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.496-5362A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34314545 | |||||||
| chr19:34314592 | T | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(206): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.496-5315T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34314592 | |||||||
| chr19:34314622 | T | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(54): Show |
58 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.496-5285T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34314622 | |||||||
| chr19:34314694 | A | C | 1 | a0001c0002t0002g0036 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.496-5213A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34314694 | |||||||
| chr19:34314694 | A | G | 2 | a0001c0001t0001g0235 a0001c0001t0001g0239 |
2 | NA18977.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.496-5213A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34314694 | |||||||
| chr19:34314892 | G | A | 19 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(16): Show |
19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.496-5015G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34314892 | |||||||
| chr19:34314915 | C | T | 1 | a0001c0002t0002g0018 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.496-4992C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34314915 | |||||||
| chr19:34315258 | G | A | 17 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(14): Show |
17 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.496-4649G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34315258 | |||||||
| chr19:34315482 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(166): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.496-4425C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34315482 | |||||||
| chr19:34315528 | G | A | 1 | a0001c0002t0002g0011 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.496-4379G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34315528 | |||||||
| chr19:34315636 | G | A | 1 | a0001c0002t0003g0152 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.496-4271G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34315636 | |||||||
| chr19:34315638 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(57): Show |
61 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.496-4269G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34315638 | |||||||
| chr19:34315710 | C | CA | 109 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(106): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.496-4175dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34315710 | ||||||
| chr19:34315710 | C | CAA | 126 | a0001c0001t0001g0081 a0001c0001t0001g0087 a0001c0001t0001g0139 others(123): Show |
126 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.496-4176_496-4175d others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34315710 | ||||||
| chr19:34315710 | C | CAAA | 15 | a0001c0001t0001g0129 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | HG01175.hp2 HG01361.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.496-4177_496-4175d others(5): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34315710 | ||||||
| chr19:34315733 | G | A | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.496-4174G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34315733 | |||||||
| chr19:34315807 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.496-4100A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34315807 | |||||||
| chr19:34315943 | G | A | 1 | a0001c0002t0015g0174 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.496-3964G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34315943 | |||||||
| chr19:34316028 | T | A | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.496-3879T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34316028 | |||||||
| chr19:34316080 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.496-3827C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34316080 | |||||||
| chr19:34316081 | G | A | 5 | a0001c0001t0009g0226 a0001c0002t0002g0011 a0001c0002t0002g0030 others(2): Show |
5 | HG00423.hp1 HG00597.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.496-3826G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34316081 | |||||||
| chr19:34316201 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.496-3706A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34316201 | |||||||
| chr19:34316295 | A | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.496-3612A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34316295 | |||||||
| chr19:34316429 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0271 |
2 | NA18981.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.496-3478C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34316429 | |||||||
| chr19:34316474 | C | A | 1 | a0008c0008t0001g0318 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.496-3433C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34316474 | |||||||
| chr19:34316636 | G | A | 42 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(39): Show |
42 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.496-3271G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34316636 | |||||||
| chr19:34316728 | G | C | 1 | a0001c0001t0001g0225 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.496-3179G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34316728 | |||||||
| chr19:34317314 | A | C | 1 | a0001c0001t0001g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.496-2593A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34317314 | |||||||
| chr19:34317325 | C | T | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.496-2582C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34317325 | |||||||
| chr19:34317336 | A | G | 4 | a0001c0001t0001g0227 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
4 | NA18962.hp1 NA18965.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-2571A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34317336 | |||||||
| chr19:34317416 | G | A | 1 | a0003c0005t0012g0320 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.496-2491G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34317416 | |||||||
| chr19:34317457 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.496-2450A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34317457 | |||||||
| chr19:34317484 | T | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(207): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.496-2423T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34317484 | |||||||
| chr19:34317505 | C | T | 6 | a0001c0001t0001g0179 a0001c0001t0001g0187 a0001c0001t0001g0206 others(3): Show |
6 | HG01891.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.496-2402C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34317505 | |||||||
| chr19:34317510 | C | T | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.496-2397C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34317510 | |||||||
| chr19:34317537 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.496-2370G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34317537 | |||||||
| chr19:34317602 | G | A | 1 | a0001c0002t0002g0047 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.496-2305G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34317602 | |||||||
| chr19:34317701 | G | A | 1 | a0001c0002t0002g0063 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.496-2206G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34317701 | |||||||
| chr19:34317865 | A | G | 4 | a0001c0001t0007g0083 a0001c0001t0007g0084 a0001c0001t0007g0146 others(1): Show |
4 | HG01123.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-2042A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34317865 | |||||||
| chr19:34318011 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.496-1896T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34318011 | |||||||
| chr19:34318036 | GGTT | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0110 a0001c0001t0001g0117 others(1): Show |
4 | HG00408.hp1 HG00621.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-1864_496-1862d others(5): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34318036 | ||||||
| chr19:34318044 | T | C | 37 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(34): Show |
37 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.496-1863T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34318044 | |||||||
| chr19:34318167 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.496-1740A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34318167 | |||||||
| chr19:34318168 | A | G | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.496-1739A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34318168 | |||||||
| chr19:34318437 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.496-1470G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34318437 | |||||||
| chr19:34318462 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(205): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.496-1445T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34318462 | |||||||
| chr19:34318619 | G | A | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.496-1288G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34318619 | |||||||
| chr19:34318824 | C | T | 2 | a0001c0002t0008g0160 a0001c0002t0015g0174 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.496-1083C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34318824 | |||||||
| chr19:34318871 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.496-1036G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34318871 | |||||||
| chr19:34319014 | C | CA | 110 | a0001c0001t0009g0226 a0001c0002t0002g0003 a0001c0002t0002g0004 others(107): Show |
110 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.496-883dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 34319014 | ||||||
| chr19:34319553 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0199 |
2 | HG01175.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.496-354G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34319553 | |||||||
| chr19:34319766 | AG | A | 20 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0256 others(17): Show |
20 | HG00140.hp1 HG00280.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.496-140delG | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34319766 | |||||||
| chr19:34319785 | T | G | 1 | a0001c0002t0002g0006 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.496-122T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 2/13 | chr19 | 34319785 | |||||||
| chr19:34320137 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.705+21A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34320137 | |||||||
| chr19:34320195 | A | G | 1 | a0001c0002t0004g0078 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.705+79A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34320195 | |||||||
| chr19:34320198 | C | T | 18 | a0001c0001t0001g0256 a0001c0001t0001g0299 a0001c0001t0001g0300 others(15): Show |
18 | HG00140.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.705+82C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34320198 | |||||||
| chr19:34320238 | A | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(57): Show |
61 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.705+122A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34320238 | |||||||
| chr19:34320447 | T | G | 2 | a0001c0002t0004g0070 a0001c0002t0004g0072 |
2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.705+331T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34320447 | |||||||
| chr19:34320529 | C | G | 1 | a0001c0001t0001g0317 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.705+413C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34320529 | |||||||
| chr19:34320727 | C | CT | 12 | a0001c0001t0001g0094 a0001c0002t0004g0068 a0001c0002t0004g0069 others(9): Show |
12 | HG00621.hp2 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.705+623dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34320727 | ||||||
| chr19:34320796 | ACTACAGC others(6): Show |
A | 4 | a0001c0001t0001g0245 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | NA18939.hp2 NA18988.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+683_705+695del others(13): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34320796 | ||||||
| chr19:34320905 | C | CT | 13 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(10): Show |
13 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.705+807dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34320905 | ||||||
| chr19:34320905 | CT | C | 43 | a0001c0001t0001g0094 a0001c0001t0001g0110 a0001c0001t0001g0117 others(40): Show |
43 | HG00408.hp1 HG00621.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.705+807delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34320905 | ||||||
| chr19:34320906 | T | C | 1 | a0001c0002t0002g0092 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.705+790T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34320906 | |||||||
| chr19:34320955 | G | A | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.705+839G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34320955 | |||||||
| chr19:34321050 | C | CTT | 55 | a0001c0001t0009g0226 a0001c0002t0002g0003 a0001c0002t0002g0004 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.705+957_705+958dup others(2): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34321050 | ||||||
| chr19:34321050 | C | CTTT | 15 | a0001c0002t0002g0008 a0001c0002t0002g0024 a0001c0002t0002g0028 others(12): Show |
15 | HG01346.hp2 HG01361.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.705+956_705+958dup others(3): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34321050 | ||||||
| chr19:34321050 | CT | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(211): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.705+958delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34321050 | ||||||
| chr19:34321050 | CTT | C | 19 | a0001c0001t0001g0216 a0001c0001t0001g0233 a0001c0001t0001g0261 others(16): Show |
19 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.705+957_705+958del others(2): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34321050 | ||||||
| chr19:34321095 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.705+979C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34321095 | |||||||
| chr19:34321158 | G | A | 1 | a0001c0001t0022g0147 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.705+1042G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34321158 | |||||||
| chr19:34321223 | A | AT | 84 | a0001c0001t0001g0080 a0001c0001t0001g0085 a0001c0001t0001g0095 others(81): Show |
84 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.705+1133dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34321223 | ||||||
| chr19:34321223 | A | ATT | 20 | a0001c0001t0001g0081 a0001c0001t0001g0088 a0001c0001t0001g0139 others(17): Show |
20 | HG00280.hp2 HG01346.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.705+1132_705+1133d others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34321223 | ||||||
| chr19:34321223 | AT | A | 9 | a0001c0001t0001g0270 a0001c0001t0001g0299 a0001c0002t0003g0162 others(6): Show |
9 | HG01256.hp1 HG01943.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.705+1133delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34321223 | ||||||
| chr19:34321223 | ATTTTTTT others(3): Show |
A | 37 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(34): Show |
37 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.705+1124_705+1133d others(12): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34321223 | ||||||
| chr19:34321223 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0325 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.705+1123_705+1133d others(13): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34321223 | ||||||
| chr19:34321223 | ATTTTTTT others(6): Show |
A | 5 | a0001c0001t0001g0090 a0001c0001t0001g0115 a0001c0001t0001g0118 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.705+1121_705+1133d others(15): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34321223 | ||||||
| chr19:34321252 | A | G | 1 | a0001c0002t0003g0154 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.705+1136A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34321252 | |||||||
| chr19:34321594 | C | T | 1 | a0001c0002t0002g0013 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.705+1478C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34321594 | |||||||
| chr19:34321614 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.705+1498C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34321614 | |||||||
| chr19:34321993 | T | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(59): Show |
63 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.705+1877T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34321993 | |||||||
| chr19:34322021 | G | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0085 others(35): Show |
39 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.705+1905G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34322021 | |||||||
| chr19:34322035 | C | T | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.705+1919C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34322035 | |||||||
| chr19:34322372 | A | G | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.705+2256A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34322372 | |||||||
| chr19:34322510 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.705+2394C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34322510 | |||||||
| chr19:34322610 | C | T | 2 | a0001c0002t0003g0153 a0001c0002t0003g0154 |
2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.705+2494C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34322610 | |||||||
| chr19:34322626 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.705+2510C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34322626 | |||||||
| chr19:34322680 | C | T | 4 | a0001c0001t0007g0083 a0001c0001t0007g0084 a0001c0001t0007g0146 others(1): Show |
4 | HG01123.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+2564C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34322680 | |||||||
| chr19:34322789 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.705+2673T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34322789 | |||||||
| chr19:34323023 | C | CT | 14 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0116 others(11): Show |
14 | HG00609.hp2 HG01981.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.705+2934dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34323023 | ||||||
| chr19:34323023 | CT | C | 186 | a0001c0001t0001g0109 a0001c0001t0001g0119 a0001c0001t0001g0214 others(183): Show |
186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.705+2934delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34323023 | ||||||
| chr19:34323023 | CTT | C | 8 | a0001c0001t0001g0227 a0001c0001t0001g0301 a0001c0001t0001g0309 others(5): Show |
8 | HG00140.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.705+2933_705+2934d others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34323023 | ||||||
| chr19:34323028 | T | C | 1 | a0009c0013t0001g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.705+2912T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34323028 | |||||||
| chr19:34323051 | G | A | 1 | a0001c0002t0002g0006 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.705+2935G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34323051 | |||||||
| chr19:34323052 | A | T | 4 | a0001c0001t0001g0215 a0001c0001t0001g0285 a0001c0001t0001g0286 others(1): Show |
4 | HG02615.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+2936A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34323052 | |||||||
| chr19:34323133 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.705+3017G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34323133 | |||||||
| chr19:34323184 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.705+3068A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34323184 | |||||||
| chr19:34323253 | G | A | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.705+3137G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34323253 | |||||||
| chr19:34323277 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | NA18985.hp1 NA18986.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.705+3161C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34323277 | |||||||
| chr19:34323391 | C | T | 1 | a0004c0010t0001g0189 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.705+3275C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34323391 | |||||||
| chr19:34323431 | A | G | 20 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0256 others(17): Show |
20 | HG00140.hp1 HG00280.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.705+3315A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34323431 | |||||||
| chr19:34323754 | C | T | 2 | a0001c0001t0001g0259 a0001c0001t0001g0262 |
2 | HG01943.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.705+3638C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34323754 | |||||||
| chr19:34324071 | C | T | 2 | a0001c0001t0001g0317 a0008c0008t0001g0318 |
2 | HG00639.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.706-3350C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34324071 | |||||||
| chr19:34324081 | G | T | 2 | a0001c0001t0001g0317 a0008c0008t0001g0318 |
2 | HG00639.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.706-3340G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34324081 | |||||||
| chr19:34324082 | C | T | 2 | a0001c0001t0001g0317 a0008c0008t0001g0318 |
2 | HG00639.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.706-3339C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34324082 | |||||||
| chr19:34324503 | CT | C | 30 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0181 others(27): Show |
30 | HG00597.hp1 HG00609.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.706-2900delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34324503 | ||||||
| chr19:34324504 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.706-2917T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34324504 | |||||||
| chr19:34324680 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0198 |
2 | HG03831.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.706-2741T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34324680 | |||||||
| chr19:34324720 | C | T | 3 | a0001c0001t0001g0145 a0001c0002t0002g0112 a0001c0002t0002g0133 |
3 | HG03831.hp2 HG04199.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.706-2701C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34324720 | |||||||
| chr19:34324901 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(62): Show |
66 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.706-2520A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34324901 | |||||||
| chr19:34325079 | ATATTCCT others(3): Show |
A | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.706-2340_706-2331d others(12): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34325079 | ||||||
| chr19:34325126 | C | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.706-2295C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34325126 | |||||||
| chr19:34325237 | C | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG00099.hp2 HG00140.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.706-2184C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34325237 | |||||||
| chr19:34325337 | T | C | 1 | a0001c0002t0004g0072 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.706-2084T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34325337 | |||||||
| chr19:34325344 | C | G | 1 | a0001c0002t0004g0072 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.706-2077C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34325344 | |||||||
| chr19:34325421 | A | T | 6 | a0001c0002t0002g0021 a0001c0002t0002g0027 a0001c0002t0002g0051 others(3): Show |
6 | HG02071.hp1 HG02080.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-2000A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34325421 | |||||||
| chr19:34325596 | C | A | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.706-1825C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34325596 | |||||||
| chr19:34325609 | C | G | 1 | a0001c0001t0001g0272 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.706-1812C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34325609 | |||||||
| chr19:34325629 | C | T | 1 | a0004c0010t0001g0189 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.706-1792C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34325629 | |||||||
| chr19:34325665 | T | G | 3 | a0002c0003t0003g0155 a0002c0003t0003g0156 a0002c0003t0003g0157 |
3 | HG01168.hp1 HG01169.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.706-1756T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34325665 | |||||||
| chr19:34325810 | T | C | 1 | a0001c0002t0008g0160 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.706-1611T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34325810 | |||||||
| chr19:34325815 | T | G | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.706-1606T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34325815 | |||||||
| chr19:34325869 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.706-1552A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34325869 | |||||||
| chr19:34326056 | C | G | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.706-1365C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34326056 | |||||||
| chr19:34326102 | C | G | 5 | a0001c0001t0001g0090 a0001c0001t0001g0115 a0001c0001t0001g0118 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.706-1319C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34326102 | |||||||
| chr19:34326211 | G | A | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.706-1210G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34326211 | |||||||
| chr19:34326240 | C | T | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.706-1181C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34326240 | |||||||
| chr19:34326376 | A | G | 4 | a0001c0001t0001g0217 a0001c0001t0001g0234 a0001c0001t0001g0244 others(1): Show |
4 | HG02074.hp2 HG02129.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.706-1045A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34326376 | |||||||
| chr19:34326562 | T | C | 18 | a0001c0001t0001g0256 a0001c0001t0001g0299 a0001c0001t0001g0300 others(15): Show |
18 | HG00140.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.706-859T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34326562 | |||||||
| chr19:34326593 | G | A | 2 | a0001c0002t0004g0073 a0001c0002t0004g0074 |
2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.706-828G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34326593 | |||||||
| chr19:34326882 | C | T | 2 | a0001c0002t0008g0160 a0001c0002t0015g0174 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.706-539C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34326882 | |||||||
| chr19:34326934 | C | G | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.706-487C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34326934 | |||||||
| chr19:34327008 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02257.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.706-413A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34327008 | |||||||
| chr19:34327154 | C | CAAAATAA others(3): Show |
21 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(18): Show |
21 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.706-244_706-235dup others(10): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34327154 | ||||||
| chr19:34327154 | CAAAAT | C | 41 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(38): Show |
41 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.706-239_706-235del others(5): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 34327154 | ||||||
| chr19:34327193 | A | T | 1 | a0006c0014t0001g0304 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.706-228A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34327193 | |||||||
| chr19:34327270 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.706-151A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 3/13 | chr19 | 34327270 | |||||||
| chr19:34327605 | A | G | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.846+44A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 4/13 | chr19 | 34327605 | |||||||
| chr19:34327654 | T | C | 6 | a0001c0001t0001g0228 a0001c0001t0001g0243 a0001c0001t0001g0246 others(3): Show |
6 | HG00621.hp1 NA18747.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.846+93T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 4/13 | chr19 | 34327654 | |||||||
| chr19:34327911 | C | T | 6 | a0001c0001t0001g0215 a0001c0001t0001g0284 a0001c0001t0001g0285 others(3): Show |
6 | HG01891.hp2 HG02280.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.942+45C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 5/13 | chr19 | 34327911 | |||||||
| chr19:34327927 | A | G | 3 | a0001c0002t0004g0070 a0001c0002t0004g0072 a0001c0002t0004g0077 |
3 | HG02258.hp1 HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.942+61A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 5/13 | chr19 | 34327927 | |||||||
| chr19:34328196 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1104+45T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34328196 | |||||||
| chr19:34328203 | C | T | 2 | a0001c0001t0001g0311 a0001c0001t0001g0313 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1104+52C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34328203 | |||||||
| chr19:34328391 | C | T | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1104+240C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34328391 | |||||||
| chr19:34328426 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1104+275A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34328426 | |||||||
| chr19:34328454 | A | C | 2 | a0001c0002t0008g0160 a0001c0002t0015g0174 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1104+303A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34328454 | |||||||
| chr19:34328527 | TA | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(159): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1104+394delA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 34328527 | ||||||
| chr19:34328527 | TAA | T | 43 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0175 others(40): Show |
43 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.1104+393_1104+394d others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 34328527 | ||||||
| chr19:34328690 | C | A | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1104+539C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34328690 | |||||||
| chr19:34328796 | C | T | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1104+645C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34328796 | |||||||
| chr19:34328979 | T | C | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1104+828T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34328979 | |||||||
| chr19:34329075 | A | T | 1 | a0001c0001t0001g0228 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1104+924A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34329075 | |||||||
| chr19:34329162 | C | T | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1104+1011C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34329162 | |||||||
| chr19:34329254 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1105-935C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34329254 | |||||||
| chr19:34329416 | C | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(53): Show |
57 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.1105-773C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34329416 | |||||||
| chr19:34329420 | T | G | 1 | a0001c0001t0022g0147 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1105-769T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34329420 | |||||||
| chr19:34329431 | G | A | 3 | a0001c0001t0001g0145 a0001c0002t0002g0112 a0001c0002t0002g0133 |
3 | HG03831.hp2 HG04199.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1105-758G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34329431 | |||||||
| chr19:34329604 | G | A | 2 | a0001c0002t0004g0073 a0001c0002t0004g0074 |
2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1105-585G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34329604 | |||||||
| chr19:34329758 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0218 |
2 | HG02647.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1105-431C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34329758 | |||||||
| chr19:34329797 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(206): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1105-392G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34329797 | |||||||
| chr19:34329843 | G | GA | 6 | a0001c0001t0001g0258 a0001c0001t0001g0269 a0001c0001t0007g0083 others(3): Show |
6 | HG01123.hp2 HG02071.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105-334dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 34329843 | ||||||
| chr19:34329942 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1105-247G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 6/13 | chr19 | 34329942 | |||||||
| chr19:34330727 | C | CT | 23 | a0001c0001t0001g0080 a0001c0001t0001g0085 a0001c0001t0001g0094 others(20): Show |
23 | HG00140.hp2 HG00609.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1263+402dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr19 | 34330727 | ||||||
| chr19:34330727 | CT | C | 33 | a0001c0001t0001g0129 a0001c0001t0001g0214 a0001c0001t0001g0256 others(30): Show |
33 | HG00140.hp1 HG00280.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1263+402delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr19 | 34330727 | ||||||
| chr19:34330727 | CTT | C | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1263+401_1263+402d others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr19 | 34330727 | ||||||
| chr19:34330746 | T | G | 1 | a0001c0001t0001g0187 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1263+399T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34330746 | |||||||
| chr19:34330746 | T | TG | 3 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 |
3 | HG02055.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1263+399_1263+400i others(3): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34330746 | |||||||
| chr19:34330748 | T | G | 44 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 others(41): Show |
44 | HG00423.hp1 HG01081.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.1263+401T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34330748 | |||||||
| chr19:34330748 | T | TG | 15 | a0001c0002t0003g0158 a0001c0002t0003g0161 a0001c0002t0003g0162 others(12): Show |
15 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1263+401_1263+402i others(3): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34330748 | |||||||
| chr19:34330901 | AT | A | 110 | a0001c0001t0001g0107 a0001c0001t0009g0226 a0001c0002t0002g0003 others(107): Show |
110 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1263+570delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr19 | 34330901 | ||||||
| chr19:34330990 | C | G | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1263+643C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34330990 | |||||||
| chr19:34331025 | G | A | 21 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 others(18): Show |
21 | HG01099.hp2 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1263+678G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34331025 | |||||||
| chr19:34331050 | C | T | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1263+703C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34331050 | |||||||
| chr19:34331208 | AAAAG | A | 18 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(15): Show |
18 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1263+865_1263+868d others(6): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr19 | 34331208 | ||||||
| chr19:34331426 | C | G | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1263+1079C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34331426 | |||||||
| chr19:34331626 | G | A | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1263+1279G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34331626 | |||||||
| chr19:34331829 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0085 others(53): Show |
57 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.1263+1482A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34331829 | |||||||
| chr19:34331884 | G | A | 1 | a0001c0002t0002g0027 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1263+1537G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34331884 | |||||||
| chr19:34331908 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1263+1561T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34331908 | |||||||
| chr19:34331991 | TA | T | 7 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0215 others(4): Show |
7 | HG01516.hp1 HG02615.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1263+1659delA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr19 | 34331991 | ||||||
| chr19:34332033 | G | A | 7 | a0001c0001t0001g0214 a0001c0001t0001g0249 a0001c0001t0001g0250 others(4): Show |
7 | HG00597.hp1 HG00609.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1264-1671G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34332033 | |||||||
| chr19:34332073 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1264-1631T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34332073 | |||||||
| chr19:34332088 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1264-1616C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34332088 | |||||||
| chr19:34332141 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1264-1563C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34332141 | |||||||
| chr19:34332163 | A | G | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1264-1541A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34332163 | |||||||
| chr19:34332328 | G | T | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1264-1376G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34332328 | |||||||
| chr19:34332335 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1264-1369A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34332335 | |||||||
| chr19:34332511 | G | A | 6 | a0001c0001t0001g0228 a0001c0001t0001g0243 a0001c0001t0001g0246 others(3): Show |
6 | HG00621.hp1 NA18747.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.1264-1193G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34332511 | |||||||
| chr19:34332964 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1264-740A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34332964 | |||||||
| chr19:34332968 | G | A | 1 | a0001c0001t0016g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1264-736G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34332968 | |||||||
| chr19:34333014 | A | G | 4 | a0001c0001t0007g0083 a0001c0001t0007g0084 a0001c0001t0007g0146 others(1): Show |
4 | HG01123.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-690A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34333014 | |||||||
| chr19:34333051 | T | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(54): Show |
58 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.1264-653T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34333051 | |||||||
| chr19:34333219 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1264-485T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34333219 | |||||||
| chr19:34333483 | C | A | 1 | a0001c0001t0001g0295 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1264-221C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | chr19 | 34333483 | |||||||
| chr19:34333677 | G | GT | 122 | a0001c0001t0001g0105 a0001c0001t0001g0135 a0001c0001t0001g0175 others(119): Show |
122 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.1264-10dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr19 | 34333677 | ||||||
| chr19:34333677 | G | GTT | 8 | a0001c0002t0002g0008 a0001c0002t0002g0030 a0001c0002t0002g0042 others(5): Show |
8 | HG00280.hp2 HG01099.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264-11_1264-10dup others(2): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr19 | 34333677 | ||||||
| chr19:34333836 | TCTGA | T | 17 | a0001c0001t0001g0215 a0001c0001t0001g0228 a0001c0001t0001g0235 others(14): Show |
17 | HG00621.hp1 HG01891.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1361+41_1361+44del others(4): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 34333836 | ||||||
| chr19:34333934 | G | A | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1361+133G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34333934 | |||||||
| chr19:34334221 | C | T | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1361+420C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34334221 | |||||||
| chr19:34334265 | A | G | 1 | a0001c0001t0007g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1361+464A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34334265 | |||||||
| chr19:34334357 | A | C | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1361+556A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34334357 | |||||||
| chr19:34334426 | C | T | 1 | a0001c0002t0002g0040 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1361+625C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34334426 | |||||||
| chr19:34334453 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1361+652C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34334453 | |||||||
| chr19:34334469 | C | T | 72 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(69): Show |
72 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1361+668C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34334469 | |||||||
| chr19:34334689 | A | G | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1361+888A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34334689 | |||||||
| chr19:34334696 | C | CA | 80 | a0001c0001t0001g0254 a0001c0001t0001g0279 a0001c0002t0002g0003 others(77): Show |
80 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1361+910dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 34334696 | ||||||
| chr19:34334713 | A | G | 3 | a0001c0001t0001g0248 a0001c0001t0001g0252 a0001c0001t0001g0294 |
3 | HG01433.hp1 NA18961.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1361+912A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34334713 | |||||||
| chr19:34334768 | A | G | 6 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 others(3): Show |
6 | HG02451.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1361+967A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34334768 | |||||||
| chr19:34334997 | C | A | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1361+1196C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34334997 | |||||||
| chr19:34334997 | C | T | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1361+1196C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34334997 | |||||||
| chr19:34335046 | G | GA | 44 | a0001c0001t0001g0082 a0001c0001t0001g0087 a0001c0001t0001g0093 others(41): Show |
44 | HG00408.hp1 HG00738.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1361+1258dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 34335046 | ||||||
| chr19:34335207 | A | G | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1361+1406A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34335207 | |||||||
| chr19:34335438 | G | A | 1 | a0001c0002t0002g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1361+1637G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34335438 | |||||||
| chr19:34335500 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1361+1699G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34335500 | |||||||
| chr19:34335507 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1361+1706A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34335507 | |||||||
| chr19:34335562 | G | A | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1361+1761G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34335562 | |||||||
| chr19:34335797 | T | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1361+1996T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34335797 | |||||||
| chr19:34335997 | T | A | 1 | a0001c0002t0002g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1361+2196T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34335997 | |||||||
| chr19:34336122 | G | A | 3 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 |
3 | HG02055.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1361+2321G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34336122 | |||||||
| chr19:34336196 | A | G | 1 | a0001c0002t0002g0125 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1361+2395A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34336196 | |||||||
| chr19:34336461 | G | A | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1361+2660G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34336461 | |||||||
| chr19:34336469 | A | AT | 7 | a0001c0001t0001g0080 a0001c0001t0001g0088 a0001c0001t0001g0098 others(4): Show |
7 | HG02135.hp1 HG02135.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1361+2685dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 34336469 | ||||||
| chr19:34336469 | AT | A | 155 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(152): Show |
155 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1361+2685delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 34336469 | ||||||
| chr19:34336541 | C | T | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1361+2740C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34336541 | |||||||
| chr19:34336844 | G | GAAAAC | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1362-3022_1362-302 others(9): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 34336844 | ||||||
| chr19:34336967 | C | CA | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1362-2894dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 34336967 | ||||||
| chr19:34337035 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1362-2832C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34337035 | |||||||
| chr19:34337050 | G | GT | 17 | a0001c0001t0001g0086 a0001c0001t0001g0108 a0001c0001t0001g0209 others(14): Show |
17 | HG01123.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1362-2800dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 34337050 | ||||||
| chr19:34337050 | GT | G | 21 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0240 others(18): Show |
21 | HG00140.hp1 HG00280.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1362-2800delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 34337050 | ||||||
| chr19:34337430 | G | A | 1 | a0001c0002t0002g0037 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1362-2437G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34337430 | |||||||
| chr19:34337487 | C | T | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1362-2380C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34337487 | |||||||
| chr19:34337595 | C | T | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1362-2272C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34337595 | |||||||
| chr19:34337762 | T | C | 73 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(70): Show |
73 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1362-2105T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34337762 | |||||||
| chr19:34337840 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0218 |
2 | HG02647.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1362-2027C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34337840 | |||||||
| chr19:34338024 | G | A | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1362-1843G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34338024 | |||||||
| chr19:34338257 | C | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG00140.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1362-1610C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34338257 | |||||||
| chr19:34338356 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1362-1511C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34338356 | |||||||
| chr19:34338362 | C | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(57): Show |
61 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1362-1505C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34338362 | |||||||
| chr19:34338451 | C | T | 72 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(69): Show |
72 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1362-1416C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34338451 | |||||||
| chr19:34338783 | A | T | 1 | a0001c0002t0002g0064 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1362-1084A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34338783 | |||||||
| chr19:34338793 | C | T | 1 | a0001c0002t0002g0036 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1362-1074C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34338793 | |||||||
| chr19:34338921 | G | A | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1362-946G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34338921 | |||||||
| chr19:34339584 | T | C | 40 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(37): Show |
40 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.1362-283T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34339584 | |||||||
| chr19:34339802 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(56): Show |
60 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.1362-65G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34339802 | |||||||
| chr19:34339836 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1362-31C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 8/13 | chr19 | 34339836 | |||||||
| chr19:34340004 | T | C | 1 | a0007c0007t0001g0255 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1487+12T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | chr19 | 34340004 | |||||||
| chr19:34340438 | T | TTTTTC | 14 | a0001c0001t0001g0218 a0001c0002t0002g0016 a0001c0002t0002g0038 others(11): Show |
14 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1487+478_1487+482d others(7): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340438 | ||||||
| chr19:34340438 | T | TTTTTCTT others(3): Show |
1 | a0001c0001t0001g0314 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1487+453_1487+454i others(12): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340438 | ||||||
| chr19:34340438 | T | TTTTTCTT others(3): Show |
149 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0214 others(146): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1487+473_1487+482d others(12): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340438 | ||||||
| chr19:34340438 | T | TTTTTCTT others(8): Show |
26 | a0001c0001t0001g0215 a0001c0001t0001g0225 a0001c0001t0001g0250 others(23): Show |
26 | HG00609.hp1 HG00639.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1487+468_1487+482d others(17): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340438 | ||||||
| chr19:34340438 | T | TTTTTCTT others(13): Show |
5 | a0001c0001t0001g0280 a0001c0002t0006g0149 a0001c0002t0006g0150 others(2): Show |
5 | HG02040.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1487+463_1487+482d others(22): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340438 | ||||||
| chr19:34340438 | T | TTTTTCTT others(18): Show |
2 | a0001c0002t0003g0153 a0001c0002t0003g0154 |
2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1487+458_1487+482d others(27): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340438 | ||||||
| chr19:34340438 | T | TTTTTCTT others(23): Show |
4 | a0001c0002t0008g0160 a0002c0003t0003g0155 a0002c0003t0003g0156 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1487+453_1487+482d others(32): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340438 | ||||||
| chr19:34340438 | T | TTTTTCTT others(28): Show |
3 | a0001c0002t0003g0158 a0001c0002t0003g0166 a0001c0002t0008g0079 |
3 | HG01993.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1487+448_1487+482d others(37): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340438 | ||||||
| chr19:34340438 | T | TTTTTCTT others(33): Show |
2 | a0001c0002t0003g0162 a0001c0002t0003g0167 |
2 | HG01361.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1487+482_1487+483i others(42): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340438 | ||||||
| chr19:34340438 | T | TTTTTCTT others(38): Show |
7 | a0001c0002t0003g0161 a0001c0002t0003g0164 a0001c0002t0003g0165 others(4): Show |
7 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1487+482_1487+483i others(47): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340438 | ||||||
| chr19:34340438 | T | TTTTTCTT others(43): Show |
2 | a0001c0002t0003g0163 a0001c0002t0003g0171 |
2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1487+482_1487+483i others(52): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340438 | ||||||
| chr19:34340438 | TTTTTC | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(92): Show |
96 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1487+478_1487+482d others(7): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340438 | ||||||
| chr19:34340438 | TTTTTCTT others(8): Show |
T | 4 | a0001c0001t0007g0083 a0001c0001t0007g0084 a0001c0001t0007g0146 others(1): Show |
4 | HG01123.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1487+468_1487+482d others(17): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340438 | ||||||
| chr19:34340448 | C | CTTTTCTT others(3): Show |
1 | a0001c0001t0001g0260 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1487+465_1487+466i others(12): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 34340448 | ||||||
| chr19:34340556 | T | C | 1 | a0001c0002t0002g0067 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1487+564T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | chr19 | 34340556 | |||||||
| chr19:34340719 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1488-703C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | chr19 | 34340719 | |||||||
| chr19:34341205 | G | A | 5 | a0001c0001t0001g0090 a0001c0001t0001g0115 a0001c0001t0001g0118 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1488-217G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | chr19 | 34341205 | |||||||
| chr19:34341261 | T | A | 17 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(14): Show |
17 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1488-161T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | chr19 | 34341261 | |||||||
| chr19:34341337 | A | G | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1488-85A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | chr19 | 34341337 | |||||||
| chr19:34341350 | A | G | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1488-72A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 9/13 | chr19 | 34341350 | |||||||
| chr19:34342478 | C | T | 20 | a0001c0001t0001g0215 a0001c0001t0001g0228 a0001c0001t0001g0232 others(17): Show |
20 | HG00621.hp1 HG01891.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.2521+23C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34342478 | |||||||
| chr19:34342489 | A | G | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2521+34A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34342489 | |||||||
| chr19:34342571 | T | C | 1 | a0001c0002t0002g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2521+116T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34342571 | |||||||
| chr19:34342579 | C | G | 6 | a0001c0001t0001g0256 a0001c0001t0001g0299 a0001c0001t0001g0305 others(3): Show |
6 | HG00280.hp1 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.2521+124C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34342579 | |||||||
| chr19:34343065 | T | A | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2521+610T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34343065 | |||||||
| chr19:34343133 | C | A | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2521+678C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34343133 | |||||||
| chr19:34343459 | G | A | 104 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(101): Show |
104 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2521+1004G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34343459 | |||||||
| chr19:34343544 | T | C | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.2521+1089T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34343544 | |||||||
| chr19:34343776 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2521+1321G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34343776 | |||||||
| chr19:34344129 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2521+1674T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34344129 | |||||||
| chr19:34344331 | C | T | 1 | a0001c0001t0001g0325 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2521+1876C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34344331 | |||||||
| chr19:34344361 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2521+1906C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34344361 | |||||||
| chr19:34344364 | G | A | 114 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(111): Show |
114 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.2521+1909G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34344364 | |||||||
| chr19:34344365 | C | T | 105 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(102): Show |
105 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.2521+1910C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34344365 | |||||||
| chr19:34344387 | G | A | 2 | a0003c0005t0012g0319 a0003c0005t0012g0320 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2521+1932G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34344387 | |||||||
| chr19:34344454 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2521+1999A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34344454 | |||||||
| chr19:34344457 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2521+2002G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34344457 | |||||||
| chr19:34344546 | C | G | 7 | a0001c0001t0001g0081 a0001c0001t0001g0139 a0001c0001t0001g0140 others(4): Show |
7 | HG02886.hp1 HG02976.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2521+2091C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34344546 | |||||||
| chr19:34344590 | C | CA | 33 | a0001c0001t0001g0081 a0001c0001t0001g0085 a0001c0001t0001g0093 others(30): Show |
33 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.2521+2151dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 34344590 | ||||||
| chr19:34344756 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2521+2301C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34344756 | |||||||
| chr19:34344840 | A | AT | 107 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0135 others(104): Show |
107 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.2521+2400dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 34344840 | ||||||
| chr19:34344840 | AT | A | 36 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(33): Show |
36 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.2521+2400delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 34344840 | ||||||
| chr19:34344854 | T | A | 3 | a0001c0002t0002g0030 a0001c0002t0010g0029 a0001c0002t0010g0048 |
3 | HG00423.hp1 NA18985.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2521+2399T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34344854 | |||||||
| chr19:34344881 | G | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(246): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.2521+2426G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34344881 | |||||||
| chr19:34344902 | G | C | 3 | a0001c0001t0001g0242 a0001c0001t0001g0265 a0001c0001t0001g0271 |
3 | NA18981.hp2 NA18993.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2521+2447G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34344902 | |||||||
| chr19:34345130 | G | T | 18 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0090 others(15): Show |
18 | HG00642.hp1 HG01109.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2521+2675G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34345130 | |||||||
| chr19:34345144 | G | A | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2521+2689G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34345144 | |||||||
| chr19:34345210 | C | T | 18 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0090 others(15): Show |
18 | HG00642.hp1 HG01109.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2522-2667C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34345210 | |||||||
| chr19:34345369 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2522-2508G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34345369 | |||||||
| chr19:34345439 | G | A | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2522-2438G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34345439 | |||||||
| chr19:34345456 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2522-2421T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34345456 | |||||||
| chr19:34345518 | C | T | 1 | a0001c0002t0002g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2522-2359C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34345518 | |||||||
| chr19:34345557 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(282): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.2522-2320T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34345557 | |||||||
| chr19:34345610 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.2522-2267A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34345610 | |||||||
| chr19:34345849 | T | C | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2522-2028T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34345849 | |||||||
| chr19:34345984 | C | T | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.2522-1893C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34345984 | |||||||
| chr19:34346012 | A | C | 2 | a0001c0002t0008g0160 a0001c0002t0015g0174 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2522-1865A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34346012 | |||||||
| chr19:34346071 | C | T | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2522-1806C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34346071 | |||||||
| chr19:34346105 | A | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(227): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2522-1772A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34346105 | |||||||
| chr19:34346428 | A | T | 5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2522-1449A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34346428 | |||||||
| chr19:34346450 | A | G | 2 | a0001c0002t0008g0160 a0001c0002t0015g0174 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2522-1427A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34346450 | |||||||
| chr19:34346464 | A | C | 1 | a0001c0001t0001g0266 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2522-1413A>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34346464 | |||||||
| chr19:34346473 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(227): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2522-1404T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34346473 | |||||||
| chr19:34346981 | T | A | 1 | a0001c0002t0006g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2522-896T>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34346981 | |||||||
| chr19:34347090 | A | AT | 14 | a0001c0001t0001g0081 a0001c0001t0001g0113 a0001c0001t0001g0139 others(11): Show |
14 | HG00597.hp1 HG01099.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.2522-771dupT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 34347090 | ||||||
| chr19:34347178 | G | A | 1 | a0001c0002t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2522-699G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34347178 | |||||||
| chr19:34347395 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2522-482C>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34347395 | |||||||
| chr19:34347456 | G | A | 8 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0139 others(5): Show |
8 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.2522-421G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34347456 | |||||||
| chr19:34347456 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2522-421G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34347456 | |||||||
| chr19:34347465 | G | C | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02886.hp1 HG02896.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.2522-412G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34347465 | |||||||
| chr19:34347537 | A | G | 1 | a0001c0002t0004g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2522-340A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34347537 | |||||||
| chr19:34347626 | C | A | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2522-251C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34347626 | |||||||
| chr19:34347634 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(227): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2522-243A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34347634 | |||||||
| chr19:34347871 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA19066.hp1 | splice_region_variant&intron_variant | LOW | c.2522-6A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 10/13 | chr19 | 34347871 | |||||||
| chr19:34348093 | C | T | 104 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(101): Show |
104 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2687+51C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 11/13 | chr19 | 34348093 | |||||||
| chr19:34348663 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2688-353T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 11/13 | chr19 | 34348663 | |||||||
| chr19:34348720 | G | A | 4 | a0001c0002t0002g0008 a0001c0002t0002g0042 a0001c0002t0002g0056 others(1): Show |
4 | HG00280.hp2 HG01099.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.2688-296G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 11/13 | chr19 | 34348720 | |||||||
| chr19:34349196 | G | T | 1 | a0001c0001t0001g0312 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2825+43G>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34349196 | |||||||
| chr19:34349323 | C | T | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.2825+170C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34349323 | |||||||
| chr19:34349729 | C | A | 104 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(101): Show |
104 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2825+576C>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34349729 | |||||||
| chr19:34349777 | C | T | 1 | a0001c0002t0002g0039 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2825+624C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34349777 | |||||||
| chr19:34349812 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2825+659T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34349812 | |||||||
| chr19:34350106 | G | A | 1 | a0001c0002t0025g0035 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2825+953G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34350106 | |||||||
| chr19:34350111 | TAAAGCAG others(20): Show |
T | 1 | a0001c0001t0001g0122 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2825+960_2825+986d others(29): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 34350111 | ||||||
| chr19:34350222 | C | T | 1 | a0001c0002t0004g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2825+1069C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34350222 | |||||||
| chr19:34350309 | C | T | 229 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(226): Show |
230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.2825+1156C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34350309 | |||||||
| chr19:34350347 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0085 others(51): Show |
55 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.2826-1167G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34350347 | |||||||
| chr19:34350356 | G | A | 19 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(16): Show |
19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2826-1158G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34350356 | |||||||
| chr19:34350726 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2826-788C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34350726 | |||||||
| chr19:34350803 | G | C | 1 | a0001c0001t0001g0315 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2826-711G>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34350803 | |||||||
| chr19:34350845 | T | G | 3 | a0001c0002t0002g0012 a0001c0002t0002g0023 a0001c0002t0002g0066 |
3 | NA18954.hp1 NA18999.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2826-669T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34350845 | |||||||
| chr19:34350877 | G | A | 1 | a0001c0002t0008g0160 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2826-637G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34350877 | |||||||
| chr19:34350921 | G | A | 104 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(101): Show |
104 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2826-593G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34350921 | |||||||
| chr19:34351069 | C | T | 2 | a0001c0002t0002g0016 a0001c0002t0002g0058 |
2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2826-445C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34351069 | |||||||
| chr19:34351169 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0085 others(51): Show |
55 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.2826-345A>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34351169 | |||||||
| chr19:34351196 | C | CA | 11 | a0001c0001t0001g0086 a0001c0001t0001g0122 a0001c0001t0001g0123 others(8): Show |
11 | HG02109.hp1 HG02717.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.2826-301dupA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 34351196 | ||||||
| chr19:34351202 | A | AT | 38 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(35): Show |
38 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.2826-312_2826-311i others(3): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34351202 | |||||||
| chr19:34351209 | A | AT | 194 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(191): Show |
195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.2826-305_2826-304i others(3): Show |
GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34351209 | |||||||
| chr19:34351209 | A | T | 41 | a0001c0001t0001g0082 a0001c0001t0001g0175 a0001c0001t0001g0176 others(38): Show |
41 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.2826-305A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34351209 | |||||||
| chr19:34351211 | A | T | 1 | a0001c0002t0002g0023 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2826-303A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34351211 | |||||||
| chr19:34351213 | AT | A | 3 | a0001c0002t0002g0059 a0001c0002t0002g0112 a0001c0002t0002g0133 |
3 | HG04199.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2826-300delT | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34351213 | |||||||
| chr19:34351216 | A | T | 1 | a0001c0002t0002g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2826-298A>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34351216 | |||||||
| chr19:34351369 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2826-145G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 12/13 | chr19 | 34351369 | |||||||
| chr19:34351763 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0009g0226 |
2 | HG02132.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.2904+171T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 13/13 | chr19 | 34351763 | |||||||
| chr19:34351766 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0201 a0001c0001t0001g0208 |
3 | HG01081.hp2 HG01358.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2904+174G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 13/13 | chr19 | 34351766 | |||||||
| chr19:34352048 | T | C | 3 | a0001c0002t0006g0149 a0001c0002t0006g0150 a0001c0002t0006g0151 |
3 | HG02809.hp2 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2904+456T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 13/13 | chr19 | 34352048 | |||||||
| chr19:34352272 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2905-375T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 13/13 | chr19 | 34352272 | |||||||
| chr19:34352275 | G | A | 19 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(16): Show |
19 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2905-372G>A | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 13/13 | chr19 | 34352275 | |||||||
| chr19:34352358 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(227): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2905-289T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 13/13 | chr19 | 34352358 | |||||||
| chr19:34352398 | T | C | 1 | a0001c0004t0002g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2905-249T>C | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 13/13 | chr19 | 34352398 | |||||||
| chr19:34352399 | CA | C | 7 | a0001c0001t0001g0116 a0001c0001t0001g0201 a0001c0001t0001g0265 others(4): Show |
7 | HG01081.hp2 HG01168.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.2905-231delA | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 34352399 | ||||||
| chr19:34352597 | T | G | 1 | a0001c0002t0004g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2905-50T>G | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 13/13 | chr19 | 34352597 | |||||||
| chr19:34352612 | C | T | 11 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(8): Show |
11 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2905-35C>T | GARRE1 | ENSG00000166398.14 | transcript | ENST00000299505.8 | protein_coding | 13/13 | chr19 | 34352612 |