Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 100271715 |
| ensemblid | ENSG00000214694.13 |
| hgncid | 37252 |
| symbol | ARHGEF33 |
| name | Rho guanine nucleotide exchange factor 33 |
| refseq_nuc | NM_001145451.5 |
| refseq_prot | NP_001138923.2 |
| ensembl_nuc | ENST00000409978.7 |
| ensembl_prot | ENSP00000387020.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 38889875 |
| end | 38975454 |
| strand | + |
| ver | v1.2 |
| region | chr2:38889875-38975454 |
| region5000 | chr2:38884875-38980454 |
| regionname0 | ARHGEF33_chr2_38889875_38975454 |
| regionname5000 | ARHGEF33_chr2_38884875_38980454 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 870 | 231 | 79 | 47 | 72 | 4 | 28 | 61 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | MEKTK others(865): Show |
chr2 | 38884875 | 38980454 |
| a0002 | 1/0 | 870 | 35 | 1 | 3 | 23 | 0 | 7 | 20 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | MEKTK others(865): Show |
chr2 | 38884875 | 38980454 |
| a0003 | 0/0 | 870 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | MEKTK others(865): Show |
chr2 | 38884875 | 38980454 |
| a0004 | 0/0 | 870 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | MEKTK others(865): Show |
chr2 | 38884875 | 38980454 |
| a0005 | 0/0 | 870 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | MEKTK others(865): Show |
chr2 | 38884875 | 38980454 |
| a0006 | 0/0 | 870 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | MEKTK others(865): Show |
chr2 | 38884875 | 38980454 |
| a0007 | 0/0 | 870 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | MEKTK others(865): Show |
chr2 | 38884875 | 38980454 |
| a0008 | 0/0 | 870 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | MEKTK others(865): Show |
chr2 | 38884875 | 38980454 |
| a0009 | 0/0 | 870 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | MEKTK others(865): Show |
chr2 | 38884875 | 38980454 |
| a0010 | 0/0 | 870 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | MEKTK others(865): Show |
chr2 | 38884875 | 38980454 |
| a0011 | 0/0 | 870 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | MEKTK others(865): Show |
chr2 | 38884875 | 38980454 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2610 | 222 | 76 | 47 | 66 | 4 | 28 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 | ||
| a0001c0003 | 0/0 | 2610 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 | ||
| a0001c0004 | 0/0 | 2610 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 | ||
| a0001c0014 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 | ||
| a0002c0002 | 1/0 | 2610 | 35 | 1 | 3 | 23 | 0 | 7 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 | ||
| a0003c0005 | 0/0 | 2610 | 3 | 0 | 2 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 | ||
| a0004c0006 | 0/0 | 2610 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 | ||
| a0005c0012 | 0/0 | 2610 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 | ||
| a0006c0010 | 0/0 | 2610 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 | ||
| a0007c0011 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 | ||
| a0008c0007 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 | ||
| a0009c0013 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 | ||
| a0010c0009 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 | ||
| a0011c0008 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | ATGGA others(2605): Show |
chr2 | 38884875 | 38980454 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4494 | 93 | 16 | 22 | 39 | 3 | 13 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0001t0002 | 0/0 | 4494 | 63 | 24 | 14 | 13 | 0 | 12 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0001t0003 | 0/0 | 4494 | 23 | 23 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0001t0004 | 0/0 | 4494 | 13 | 8 | 1 | 4 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0001t0005 | 0/0 | 4494 | 8 | 1 | 4 | 0 | 1 | 2 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0001t0006 | 0/0 | 4492 | 10 | 0 | 2 | 8 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4487): Show |
chr2 | 38884875 | 38980454 |
| a0001c0001t0007 | 0/0 | 4496 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4491): Show |
chr2 | 38884875 | 38980454 |
| a0001c0001t0008 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0001t0009 | 0/0 | 4494 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0001t0010 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0001t0013 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0001t0014 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4487): Show |
chr2 | 38884875 | 38980454 |
| a0001c0001t0017 | 0/1 | 4494 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0001t0018 | 0/0 | 4494 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0003t0002 | 0/0 | 4494 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0003t0004 | 0/0 | 4494 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0003t0015 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0004t0004 | 0/0 | 4494 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0004t0011 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0001c0014t0002 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0002c0002t0001 | 0/0 | 4494 | 30 | 1 | 1 | 22 | 0 | 6 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0002c0002t0002 | 1/0 | 4494 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0002c0002t0004 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0002c0002t0005 | 0/0 | 4494 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0002c0002t0008 | 0/0 | 4494 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0003c0005t0001 | 0/0 | 4494 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0003c0005t0012 | 0/0 | 4496 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4491): Show |
chr2 | 38884875 | 38980454 |
| a0004c0006t0001 | 0/0 | 4494 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0005c0012t0002 | 0/0 | 4494 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0006c0010t0005 | 0/0 | 4494 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0007c0011t0016 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0008c0007t0001 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0009c0013t0001 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0010c0009t0001 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| a0011c0008t0004 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | GTTTC others(4489): Show |
chr2 | 38884875 | 38980454 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0006g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0007g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0007g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0009g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0010g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0013g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0014g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0017g0032 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0001t0018g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0003t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0003t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0003t0015g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0004t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0004t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0004t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0001c0014t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0002g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0002c0002t0008g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0003c0005t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0003c0005t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0003c0005t0012g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0004c0006t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0004c0006t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0005c0012t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0006c0010t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0007c0011t0016g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0008c0007t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0009c0013t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0010c0009t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| a0011c0008t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | FIN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | CHS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG00738 | hp1 | a0004 | c0006 | t0001 | g0102 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0064 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01069 | hp2 | a0002 | c0002 | t0005 | g0068 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01071 | hp1 | a0002 | c0002 | t0005 | g0067 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0046 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01081 | hp2 | a0004 | c0006 | t0001 | g0100 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0251 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0039 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01257 | hp1 | a0003 | c0005 | t0012 | g0002 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01258 | hp2 | a0003 | c0005 | t0001 | g0002 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0061 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01358 | hp2 | a0001 | c0001 | t0007 | g0033 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0212 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0065 | EUR | IBS | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01978 | hp1 | a0005 | c0012 | t0002 | g0034 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01981 | hp1 | a0006 | c0010 | t0005 | g0063 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0250 | AMR | PEL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | KHV | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0249 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | CDX | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0005 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0267 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02602 | hp1 | a0001 | c0001 | t0018 | g0011 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0180 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02615 | hp2 | a0001 | c0004 | t0004 | g0076 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02622 | hp2 | a0001 | c0004 | t0004 | g0075 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02723 | hp2 | a0007 | c0011 | t0016 | g0210 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0010 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02809 | hp2 | a0001 | c0004 | t0011 | g0077 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0262 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0245 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0213 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0166 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03017 | hp2 | a0003 | c0005 | t0001 | g0140 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0268 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03710 | hp1 | a0002 | c0002 | t0008 | g0197 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | BEB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0185 | SAS | BEB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0181 | SAS | BEB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | BEB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0176 | SAS | STU | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | STU | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0189 | SAS | STU | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | STU | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0179 | SAS | STU | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | YRI | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0005 | AFR | YRI | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0266 | AFR | YRI | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18952 | hp2 | a0001 | c0001 | t0006 | g0255 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18953 | hp2 | a0008 | c0007 | t0001 | g0170 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18956 | hp1 | a0001 | c0001 | t0006 | g0257 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18961 | hp1 | a0001 | c0001 | t0006 | g0258 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18964 | hp1 | a0001 | c0001 | t0013 | g0145 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18977 | hp2 | a0010 | c0009 | t0001 | g0128 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18988 | hp2 | a0002 | c0002 | t0004 | g0206 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18991 | hp2 | a0001 | c0003 | t0002 | g0272 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18993 | hp2 | a0001 | c0003 | t0004 | g0204 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18997 | hp1 | a0001 | c0001 | t0006 | g0239 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19003 | hp2 | a0001 | c0001 | t0006 | g0254 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19012 | hp1 | a0001 | c0003 | t0015 | g0173 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | LWK | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | LWK | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19043 | hp2 | a0011 | c0008 | t0004 | g0214 | AFR | LWK | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19058 | hp1 | a0001 | c0001 | t0014 | g0094 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19060 | hp1 | a0001 | c0014 | t0002 | g0056 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19068 | hp2 | a0001 | c0001 | t0006 | g0256 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19077 | hp1 | a0001 | c0003 | t0004 | g0205 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19079 | hp1 | a0001 | c0003 | t0002 | g0271 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19083 | hp1 | a0001 | c0001 | t0006 | g0253 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | YRI | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | YRI | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | ASW | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ASW | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0013 | SAS | GIH | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | GIH | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | MSL | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18955 | hp1 | a0009 | c0013 | t0001 | g0186 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | USA | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | USA | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0017 | g0032 | REF | REF | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0219 | REF | REF | ARHGEF33_chr2_38884875_38980454 | ARHGEF33 | chr2 | 38884875 | 38980454 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38928925 | G | A | 1 | a0008 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.94G>A | p.Glu32Lys | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/18 | 364/4494 | 94/2613 | 32/870 | chr2 | 38928925 | |||
| chr2:38931156 | C | G | 1 | a0003 | 3 | HG01257.hp1 HG01258.hp2 HG03017.hp2 |
missense_variant | MODERATE | c.410C>G | p.Ala137Gly | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/18 | 680/4494 | 410/2613 | 137/870 | chr2 | 38931156 | |||
| chr2:38937535 | G | A | 1 | a0011 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.766G>A | p.Val256Ile | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/18 | 1036/4494 | 766/2613 | 256/870 | chr2 | 38937535 | |||
| chr2:38953177 | T | C | 1 | a0010 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.1069T>C | p.Tyr357His | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/18 | 1339/4494 | 1069/2613 | 357/870 | chr2 | 38953177 | |||
| chr2:38959867 | G | C | 1 | a0006 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.1562G>C | p.Ser521Thr | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 1832/4494 | 1562/2613 | 521/870 | chr2 | 38959867 | |||
| chr2:38960049 | T | C | 9 | a0001 a0003 a0004 others(6): Show |
241 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(238): Show |
missense_variant | MODERATE | c.1744T>C | p.Ser582Pro | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2014/4494 | 1744/2613 | 582/870 | chr2 | 38960049 | |||
| chr2:38960076 | G | T | 1 | a0004 | 2 | HG00738.hp1 HG01081.hp2 |
missense_variant | MODERATE | c.1771G>T | p.Val591Leu | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2041/4494 | 1771/2613 | 591/870 | chr2 | 38960076 | |||
| chr2:38960196 | G | A | 1 | a0009 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.1891G>A | p.Glu631Lys | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2161/4494 | 1891/2613 | 631/870 | chr2 | 38960196 | |||
| chr2:38960551 | C | G | 1 | a0005 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.2246C>G | p.Pro749Arg | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2516/4494 | 2246/2613 | 749/870 | chr2 | 38960551 | |||
| chr2:38960581 | C | T | 1 | a0007 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.2276C>T | p.Ala759Val | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2546/4494 | 2276/2613 | 759/870 | chr2 | 38960581 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38928966 | A | G | 1 | a0001c0014 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.135A>G | p.Ser45Ser | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/18 | 405/4494 | 135/2613 | 45/870 | chr2 | 38928966 | |||
| chr2:38960378 | A | G | 9 | a0001c0001 a0001c0014 a0003c0005 others(6): Show |
232 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(229): Show |
synonymous_variant | LOW | c.2073A>G | p.Lys691Lys | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2343/4494 | 2073/2613 | 691/870 | chr2 | 38960378 | |||
| chr2:38960450 | G | C | 1 | a0001c0004 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.2145G>C | p.Ala715Ala | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2415/4494 | 2145/2613 | 715/870 | chr2 | 38960450 | |||
| chr2:38960525 | C | T | 1 | a0007c0011 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.2220C>T | p.Ala740Ala | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/18 | 2490/4494 | 2220/2613 | 740/870 | chr2 | 38960525 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38889976 | G | A | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(17): Show |
157 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(154): Show |
5_prime_UTR_variant | MODIFIER | c.-169G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/18 | 29472 | chr2 | 38889976 | ||||||
| chr2:38895800 | A | C | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(14): Show |
148 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(145): Show |
5_prime_UTR_variant | MODIFIER | c.-135A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/18 | 23648 | chr2 | 38895800 | ||||||
| chr2:38973911 | A | AAT | 2 | a0001c0001t0007 a0003c0005t0012 |
5 | HG00741.hp2 HG01081.hp1 HG01167.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*81_*82dupAT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 83 | INFO_REALIGN_3_PRIME | chr2 | 38973911 | |||||
| chr2:38973928 | A | G | 1 | a0001c0003t0015 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*85A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 85 | chr2 | 38973928 | ||||||
| chr2:38973932 | CTA | C | 2 | a0001c0001t0006 a0001c0001t0014 |
11 | HG01106.hp2 HG01993.hp2 NA18952.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*105_*106delAT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 105 | INFO_REALIGN_3_PRIME | chr2 | 38973932 | |||||
| chr2:38973938 | A | C | 1 | a0001c0001t0018 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*95A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 95 | chr2 | 38973938 | ||||||
| chr2:38974668 | A | G | 1 | a0001c0001t0009 | 2 | HG02280.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*825A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 825 | chr2 | 38974668 | ||||||
| chr2:38975241 | A | G | 2 | a0001c0001t0008 a0002c0002t0008 |
2 | HG02976.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1398A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 1398 | chr2 | 38975241 | ||||||
| chr2:38975340 | T | G | 1 | a0007c0011t0016 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1497T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 1497 | chr2 | 38975340 | ||||||
| chr2:38975352 | G | A | 1 | a0001c0001t0013 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1509G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 1509 | chr2 | 38975352 | ||||||
| chr2:38975378 | C | T | 1 | a0001c0004t0011 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1535C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 1535 | chr2 | 38975378 | ||||||
| chr2:38975446 | A | G | 4 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0010 others(1): Show |
35 | HG01106.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1603A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 18/18 | 1603 | chr2 | 38975446 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38890048 | T | C | 2 | a0001c0001t0002g0006 a0001c0001t0002g0007 |
2 | HG01109.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-159+62T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890048 | |||||||
| chr2:38890059 | C | G | 5 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0009g0005 others(2): Show |
6 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-159+73C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890059 | |||||||
| chr2:38890144 | T | G | 65 | a0001c0001t0001g0066 a0001c0001t0002g0006 a0001c0001t0002g0007 others(62): Show |
65 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.-159+158T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890144 | |||||||
| chr2:38890164 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-159+178T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890164 | |||||||
| chr2:38890225 | C | T | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-159+239C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890225 | |||||||
| chr2:38890266 | A | G | 7 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0004g0261 others(4): Show |
7 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-159+280A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890266 | |||||||
| chr2:38890477 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(224): Show |
231 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(228): Show |
intron_variant | MODIFIER | c.-159+491T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890477 | |||||||
| chr2:38890513 | G | C | 4 | a0001c0001t0002g0004 a0001c0001t0002g0215 a0001c0001t0002g0216 others(1): Show |
5 | HG01496.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+527G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890513 | |||||||
| chr2:38890615 | G | A | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-159+629G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890615 | |||||||
| chr2:38890675 | A | G | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-159+689A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890675 | |||||||
| chr2:38890765 | T | C | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-159+779T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890765 | |||||||
| chr2:38890956 | A | G | 3 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0010g0213 |
3 | HG01361.hp2 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-159+970A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890956 | |||||||
| chr2:38890962 | C | G | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-159+976C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890962 | |||||||
| chr2:38890968 | G | GT | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(242): Show |
249 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(246): Show |
intron_variant | MODIFIER | c.-159+995dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38890968 | ||||||
| chr2:38890987 | T | G | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-159+1001T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38890987 | |||||||
| chr2:38891064 | A | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(267): Show |
275 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(272): Show |
intron_variant | MODIFIER | c.-159+1078A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891064 | |||||||
| chr2:38891133 | C | G | 3 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-159+1147C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891133 | |||||||
| chr2:38891247 | T | C | 4 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0004g0261 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-159+1261T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891247 | |||||||
| chr2:38891402 | T | C | 62 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(59): Show |
62 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.-159+1416T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891402 | |||||||
| chr2:38891427 | A | G | 2 | a0001c0001t0003g0209 a0007c0011t0016g0210 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-159+1441A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891427 | |||||||
| chr2:38891537 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-159+1551T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891537 | |||||||
| chr2:38891620 | T | A | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-159+1634T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891620 | |||||||
| chr2:38891850 | T | A | 4 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-159+1864T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891850 | |||||||
| chr2:38891877 | C | T | 5 | a0001c0001t0003g0209 a0001c0001t0004g0266 a0001c0001t0004g0267 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+1891C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891877 | |||||||
| chr2:38891925 | C | T | 12 | a0001c0001t0003g0248 a0001c0001t0003g0249 a0001c0001t0006g0239 others(9): Show |
12 | HG01106.hp2 HG01993.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-159+1939C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38891925 | |||||||
| chr2:38892056 | T | C | 5 | a0001c0001t0001g0079 a0002c0002t0001g0078 a0002c0002t0001g0080 others(2): Show |
5 | HG02135.hp2 NA18956.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+2070T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892056 | |||||||
| chr2:38892075 | A | T | 5 | a0001c0001t0003g0209 a0001c0001t0004g0266 a0001c0001t0004g0267 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+2089A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892075 | |||||||
| chr2:38892408 | G | A | 2 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-159+2422G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892408 | |||||||
| chr2:38892421 | A | ATC | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(144): Show |
150 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.-159+2436_-159+243 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38892421 | ||||||
| chr2:38892585 | T | A | 4 | a0001c0001t0003g0209 a0001c0001t0004g0266 a0001c0001t0004g0267 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-159+2599T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892585 | |||||||
| chr2:38892647 | A | G | 2 | a0001c0001t0003g0209 a0007c0011t0016g0210 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-159+2661A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892647 | |||||||
| chr2:38892712 | A | G | 5 | a0001c0001t0001g0207 a0001c0001t0004g0208 a0001c0003t0004g0204 others(2): Show |
5 | HG00558.hp1 NA18949.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.-159+2726A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892712 | |||||||
| chr2:38892771 | A | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-159+2785A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892771 | |||||||
| chr2:38892920 | TTCCTC | T | 3 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0001g0087 |
3 | NA18945.hp2 NA18980.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-158-2855_-158-285 others(9): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38892920 | ||||||
| chr2:38892943 | A | G | 4 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0004g0261 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158-2834A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38892943 | |||||||
| chr2:38893093 | A | G | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-158-2684A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893093 | |||||||
| chr2:38893157 | CT | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(228): Show |
235 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.-158-2604delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38893157 | ||||||
| chr2:38893157 | CTT | C | 6 | a0001c0001t0001g0088 a0001c0001t0002g0008 a0001c0001t0004g0259 others(3): Show |
6 | HG02818.hp2 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-158-2605_-158-260 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38893157 | ||||||
| chr2:38893263 | A | G | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-158-2514A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893263 | |||||||
| chr2:38893335 | C | T | 5 | a0001c0001t0003g0209 a0001c0001t0004g0266 a0001c0001t0004g0267 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-2442C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893335 | |||||||
| chr2:38893639 | A | G | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-158-2138A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893639 | |||||||
| chr2:38893662 | A | G | 10 | a0001c0001t0006g0239 a0001c0001t0006g0250 a0001c0001t0006g0251 others(7): Show |
10 | HG01106.hp2 HG01993.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.-158-2115A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893662 | |||||||
| chr2:38893699 | T | C | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-158-2078T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893699 | |||||||
| chr2:38893712 | A | C | 4 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158-2065A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893712 | |||||||
| chr2:38893766 | C | G | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-158-2011C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893766 | |||||||
| chr2:38893785 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18942.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-158-1992C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893785 | |||||||
| chr2:38893829 | A | G | 77 | a0001c0001t0001g0083 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
78 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.-158-1948A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893829 | |||||||
| chr2:38893890 | G | A | 5 | a0001c0001t0003g0209 a0001c0001t0004g0266 a0001c0001t0004g0267 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-1887G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38893890 | |||||||
| chr2:38894001 | A | G | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0009g0005 |
4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-158-1776A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894001 | |||||||
| chr2:38894044 | C | A | 1 | a0001c0001t0002g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-158-1733C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894044 | |||||||
| chr2:38894332 | T | TA | 67 | a0001c0001t0001g0083 a0001c0001t0002g0006 a0001c0001t0002g0007 others(64): Show |
67 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.-158-1433dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38894332 | ||||||
| chr2:38894423 | G | GA | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(239): Show |
245 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(242): Show |
intron_variant | MODIFIER | c.-158-1343dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38894423 | ||||||
| chr2:38894423 | G | GAA | 6 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0006g0239 others(3): Show |
7 | HG02280.hp1 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-158-1344_-158-134 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38894423 | ||||||
| chr2:38894438 | T | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(222): Show |
229 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(226): Show |
intron_variant | MODIFIER | c.-158-1339T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894438 | |||||||
| chr2:38894441 | T | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | NA19012.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-158-1336T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894441 | |||||||
| chr2:38894487 | AAAAC | A | 7 | a0001c0001t0002g0222 a0001c0001t0004g0259 a0001c0001t0004g0260 others(4): Show |
7 | HG01516.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-158-1271_-158-126 others(8): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38894487 | ||||||
| chr2:38894549 | C | G | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-158-1228C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894549 | |||||||
| chr2:38894593 | C | A | 2 | a0001c0001t0003g0209 a0007c0011t0016g0210 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-158-1184C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894593 | |||||||
| chr2:38894716 | C | G | 42 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(39): Show |
42 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-158-1061C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38894716 | |||||||
| chr2:38895202 | A | G | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0009g0005 |
4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-158-575A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895202 | |||||||
| chr2:38895228 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | NA19012.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-158-549C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895228 | |||||||
| chr2:38895313 | C | T | 1 | a0001c0001t0004g0208 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-158-464C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895313 | |||||||
| chr2:38895316 | T | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-158-461T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895316 | |||||||
| chr2:38895316 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(221): Show |
228 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.-158-461T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895316 | |||||||
| chr2:38895485 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(134): Show |
140 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.-158-292C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895485 | |||||||
| chr2:38895719 | G | A | 5 | a0001c0001t0003g0209 a0001c0001t0004g0266 a0001c0001t0004g0267 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-58G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895719 | |||||||
| chr2:38895754 | GT | G | 6 | a0001c0001t0001g0202 a0001c0001t0003g0209 a0001c0001t0004g0266 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.-158-5delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 38895754 | ||||||
| chr2:38895758 | T | TG | 6 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0006g0239 others(3): Show |
7 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-158-19_-158-18ins others(1): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895758 | |||||||
| chr2:38895759 | T | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(231): Show |
237 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(234): Show |
intron_variant | MODIFIER | c.-158-18T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895759 | |||||||
| chr2:38895760 | T | G | 4 | a0001c0001t0001g0202 a0001c0001t0004g0266 a0001c0001t0004g0267 others(1): Show |
4 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158-17T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 1/17 | chr2 | 38895760 | |||||||
| chr2:38895888 | C | T | 4 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+39C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38895888 | |||||||
| chr2:38896018 | T | C | 1 | a0001c0001t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-86+169T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896018 | |||||||
| chr2:38896048 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-86+199C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896048 | |||||||
| chr2:38896079 | G | A | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-86+230G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896079 | |||||||
| chr2:38896098 | A | G | 5 | a0001c0001t0003g0209 a0001c0001t0004g0266 a0001c0001t0004g0267 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+249A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896098 | |||||||
| chr2:38896105 | T | C | 20 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0003g0242 others(17): Show |
20 | HG01106.hp2 HG01884.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.-86+256T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896105 | |||||||
| chr2:38896110 | A | C | 2 | a0002c0002t0001g0199 a0002c0002t0001g0200 |
2 | NA18977.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-86+261A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896110 | |||||||
| chr2:38896285 | C | A | 1 | a0001c0001t0003g0249 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-86+436C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896285 | |||||||
| chr2:38896340 | G | A | 2 | a0001c0001t0006g0250 a0001c0001t0006g0251 |
2 | HG01106.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-86+491G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896340 | |||||||
| chr2:38896360 | A | G | 20 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0003g0242 others(17): Show |
20 | HG01106.hp2 HG01884.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.-86+511A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896360 | |||||||
| chr2:38896397 | G | A | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0009g0005 |
4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+548G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896397 | |||||||
| chr2:38896430 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-86+581G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896430 | |||||||
| chr2:38896450 | A | T | 1 | a0001c0001t0002g0060 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-86+601A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896450 | |||||||
| chr2:38896452 | T | A | 1 | a0001c0001t0002g0060 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-86+603T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896452 | |||||||
| chr2:38896454 | A | T | 1 | a0001c0001t0002g0060 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-86+605A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896454 | |||||||
| chr2:38896572 | G | T | 4 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+723G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896572 | |||||||
| chr2:38896578 | G | T | 4 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+729G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896578 | |||||||
| chr2:38896649 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(243): Show |
250 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(247): Show |
intron_variant | MODIFIER | c.-86+800T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896649 | |||||||
| chr2:38896685 | G | A | 1 | a0001c0001t0003g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-86+836G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896685 | |||||||
| chr2:38896907 | G | A | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-86+1058G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38896907 | |||||||
| chr2:38897027 | T | A | 2 | a0001c0001t0003g0209 a0007c0011t0016g0210 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+1178T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897027 | |||||||
| chr2:38897041 | G | A | 2 | a0001c0001t0006g0252 a0001c0001t0006g0253 |
2 | NA18982.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-86+1192G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897041 | |||||||
| chr2:38897059 | G | A | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0009g0005 |
4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+1210G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897059 | |||||||
| chr2:38897119 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(142): Show |
148 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.-86+1270T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897119 | |||||||
| chr2:38897156 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(138): Show |
144 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.-86+1307C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897156 | |||||||
| chr2:38897165 | C | A | 1 | a0001c0001t0014g0094 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-86+1316C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897165 | |||||||
| chr2:38897193 | C | T | 1 | a0002c0002t0001g0198 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-86+1344C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897193 | |||||||
| chr2:38897266 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-86+1417T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897266 | |||||||
| chr2:38897328 | T | C | 2 | a0001c0001t0003g0209 a0007c0011t0016g0210 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+1479T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897328 | |||||||
| chr2:38897368 | A | G | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-86+1519A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897368 | |||||||
| chr2:38897419 | C | T | 1 | a0001c0001t0004g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-86+1570C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897419 | |||||||
| chr2:38897586 | G | A | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+1737G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897586 | |||||||
| chr2:38897618 | A | T | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+1769A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897618 | |||||||
| chr2:38897677 | C | T | 4 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+1828C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897677 | |||||||
| chr2:38897814 | T | C | 53 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(50): Show |
53 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.-86+1965T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897814 | |||||||
| chr2:38897856 | A | T | 1 | a0002c0002t0008g0197 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-86+2007A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897856 | |||||||
| chr2:38897886 | G | A | 1 | a0001c0001t0003g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-86+2037G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38897886 | |||||||
| chr2:38898135 | A | G | 9 | a0001c0001t0001g0083 a0001c0001t0005g0012 a0001c0001t0005g0013 others(6): Show |
9 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-86+2286A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898135 | |||||||
| chr2:38898229 | A | G | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+2380A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898229 | |||||||
| chr2:38898342 | A | G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | HG02717.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-86+2493A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898342 | |||||||
| chr2:38898373 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-86+2524G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898373 | |||||||
| chr2:38898413 | C | T | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+2564C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898413 | |||||||
| chr2:38898461 | C | G | 1 | a0001c0001t0003g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-86+2612C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898461 | |||||||
| chr2:38898473 | C | T | 4 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0004g0261 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+2624C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898473 | |||||||
| chr2:38898886 | A | G | 1 | a0001c0001t0002g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-86+3037A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38898886 | |||||||
| chr2:38899027 | AT | A | 7 | a0001c0001t0001g0202 a0001c0001t0003g0209 a0001c0004t0004g0075 others(4): Show |
7 | HG02615.hp2 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+3188delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38899027 | ||||||
| chr2:38899107 | T | C | 1 | a0001c0001t0002g0026 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-86+3258T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899107 | |||||||
| chr2:38899121 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-86+3272C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899121 | |||||||
| chr2:38899145 | A | G | 7 | a0001c0001t0004g0208 a0001c0001t0004g0263 a0001c0001t0004g0264 others(4): Show |
7 | NA18949.hp1 NA18961.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+3296A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899145 | |||||||
| chr2:38899257 | C | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(223): Show |
230 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(227): Show |
intron_variant | MODIFIER | c.-86+3408C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899257 | |||||||
| chr2:38899284 | A | G | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+3435A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899284 | |||||||
| chr2:38899357 | T | A | 2 | a0002c0002t0001g0096 a0002c0002t0001g0198 |
2 | NA18986.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-86+3508T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899357 | |||||||
| chr2:38899663 | T | C | 1 | a0001c0001t0003g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-86+3814T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899663 | |||||||
| chr2:38899698 | G | T | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+3849G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899698 | |||||||
| chr2:38899737 | G | A | 2 | a0002c0002t0005g0067 a0002c0002t0005g0068 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-86+3888G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899737 | |||||||
| chr2:38899739 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-86+3890G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899739 | |||||||
| chr2:38899879 | G | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(2): Show |
5 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+4030G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38899879 | |||||||
| chr2:38900026 | CA | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(163): Show |
169 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.-86+4187delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38900026 | ||||||
| chr2:38900106 | T | C | 18 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(15): Show |
18 | HG01069.hp1 HG01070.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-86+4257T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900106 | |||||||
| chr2:38900213 | A | G | 40 | a0001c0001t0001g0079 a0001c0001t0001g0178 a0001c0001t0001g0183 others(37): Show |
40 | HG00597.hp2 HG01123.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.-86+4364A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900213 | |||||||
| chr2:38900350 | C | T | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+4501C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900350 | |||||||
| chr2:38900428 | T | C | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+4579T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900428 | |||||||
| chr2:38900606 | T | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | NA18945.hp1 NA18952.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-86+4757T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900606 | |||||||
| chr2:38900679 | C | G | 20 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0003g0242 others(17): Show |
20 | HG01106.hp2 HG01884.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.-86+4830C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900679 | |||||||
| chr2:38900788 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-86+4939C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900788 | |||||||
| chr2:38900969 | C | G | 3 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-86+5120C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38900969 | |||||||
| chr2:38901031 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG00738.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-86+5182C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901031 | |||||||
| chr2:38901433 | C | T | 1 | a0001c0001t0003g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-86+5584C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901433 | |||||||
| chr2:38901469 | C | T | 71 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(68): Show |
72 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.-86+5620C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901469 | |||||||
| chr2:38901485 | C | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(149): Show |
155 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.-86+5636C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901485 | |||||||
| chr2:38901493 | G | A | 1 | a0001c0001t0002g0223 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-86+5644G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901493 | |||||||
| chr2:38901578 | C | T | 12 | a0001c0001t0003g0248 a0001c0001t0003g0249 a0001c0001t0006g0239 others(9): Show |
12 | HG01106.hp2 HG01993.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-86+5729C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901578 | |||||||
| chr2:38901798 | C | T | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+5949C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38901798 | |||||||
| chr2:38902018 | G | C | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-86+6169G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902018 | |||||||
| chr2:38902071 | C | T | 3 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-86+6222C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902071 | |||||||
| chr2:38902134 | GA | G | 6 | a0001c0001t0002g0027 a0001c0001t0002g0071 a0001c0001t0004g0266 others(3): Show |
6 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+6303delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38902134 | ||||||
| chr2:38902274 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-86+6425C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902274 | |||||||
| chr2:38902381 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(126): Show |
132 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.-86+6532G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902381 | |||||||
| chr2:38902409 | A | C | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-86+6560A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902409 | |||||||
| chr2:38902475 | G | C | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0009g0005 |
4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+6626G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902475 | |||||||
| chr2:38902521 | A | G | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+6672A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902521 | |||||||
| chr2:38902539 | C | G | 3 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-86+6690C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902539 | |||||||
| chr2:38902794 | A | G | 58 | a0001c0001t0001g0066 a0001c0001t0002g0006 a0001c0001t0002g0007 others(55): Show |
58 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.-86+6945A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902794 | |||||||
| chr2:38902870 | T | G | 2 | a0001c0001t0003g0209 a0007c0011t0016g0210 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+7021T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38902870 | |||||||
| chr2:38903000 | T | G | 1 | a0001c0001t0006g0239 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-86+7151T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903000 | |||||||
| chr2:38903049 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-86+7200G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903049 | |||||||
| chr2:38903057 | A | G | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-86+7208A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903057 | |||||||
| chr2:38903071 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-86+7222T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903071 | |||||||
| chr2:38903192 | A | C | 54 | a0001c0001t0001g0066 a0001c0001t0002g0006 a0001c0001t0002g0007 others(51): Show |
54 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.-86+7343A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903192 | |||||||
| chr2:38903223 | A | G | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+7374A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903223 | |||||||
| chr2:38903239 | TA | T | 9 | a0001c0001t0003g0209 a0001c0001t0004g0208 a0001c0001t0004g0263 others(6): Show |
9 | HG02723.hp2 HG03471.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.-86+7398delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38903239 | ||||||
| chr2:38903286 | A | G | 5 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0009g0005 others(2): Show |
6 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-86+7437A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903286 | |||||||
| chr2:38903310 | A | G | 2 | a0001c0001t0005g0014 a0001c0001t0005g0015 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-86+7461A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903310 | |||||||
| chr2:38903349 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-86+7500T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903349 | |||||||
| chr2:38903417 | A | AT | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(133): Show |
139 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.-86+7581dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38903417 | ||||||
| chr2:38903576 | C | T | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-86+7727C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903576 | |||||||
| chr2:38903957 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-86+8108A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38903957 | |||||||
| chr2:38904142 | G | C | 53 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(50): Show |
53 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.-86+8293G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904142 | |||||||
| chr2:38904231 | T | C | 15 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(12): Show |
15 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-86+8382T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904231 | |||||||
| chr2:38904264 | C | T | 1 | a0002c0002t0004g0206 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-86+8415C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904264 | |||||||
| chr2:38904280 | A | G | 5 | a0001c0001t0002g0055 a0001c0001t0002g0057 a0001c0001t0002g0058 others(2): Show |
5 | NA18960.hp2 NA18988.hp1 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86+8431A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904280 | |||||||
| chr2:38904317 | G | A | 1 | a0001c0003t0004g0204 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-86+8468G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904317 | |||||||
| chr2:38904395 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-86+8546C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904395 | |||||||
| chr2:38904415 | GA | G | 53 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(50): Show |
53 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.-86+8572delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38904415 | ||||||
| chr2:38904471 | T | C | 2 | a0001c0001t0002g0028 a0001c0001t0002g0029 |
2 | HG02698.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-86+8622T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904471 | |||||||
| chr2:38904639 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(151): Show |
157 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.-86+8790A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904639 | |||||||
| chr2:38904690 | G | A | 16 | a0001c0001t0003g0209 a0001c0001t0004g0208 a0001c0001t0004g0211 others(13): Show |
16 | HG01361.hp2 HG02723.hp2 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.-86+8841G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904690 | |||||||
| chr2:38904694 | C | A | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-86+8845C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904694 | |||||||
| chr2:38904694 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-86+8845C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904694 | |||||||
| chr2:38904695 | G | A | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-86+8846G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904695 | |||||||
| chr2:38904707 | C | CA | 9 | a0001c0001t0003g0209 a0001c0001t0004g0266 a0001c0001t0004g0267 others(6): Show |
9 | HG02572.hp2 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-86+8873dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38904707 | ||||||
| chr2:38904707 | C | CAA | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(130): Show |
136 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.-86+8872_-86+8873d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38904707 | ||||||
| chr2:38904707 | C | CAAA | 6 | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0113 others(3): Show |
6 | HG03942.hp2 NA18977.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.-86+8871_-86+8873d others(5): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38904707 | ||||||
| chr2:38904707 | CA | C | 52 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(49): Show |
52 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-86+8873delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38904707 | ||||||
| chr2:38904713 | A | G | 3 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0010g0213 |
3 | HG01361.hp2 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-86+8864A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904713 | |||||||
| chr2:38904816 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(145): Show |
151 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.-86+8967G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904816 | |||||||
| chr2:38904827 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-86+8978G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904827 | |||||||
| chr2:38904989 | G | A | 1 | a0002c0002t0001g0086 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-86+9140G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38904989 | |||||||
| chr2:38905057 | G | A | 9 | a0001c0001t0001g0073 a0001c0001t0001g0103 a0001c0001t0001g0104 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-86+9208G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38905057 | |||||||
| chr2:38905068 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-86+9219A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38905068 | |||||||
| chr2:38905383 | A | G | 2 | a0001c0001t0005g0065 a0006c0010t0005g0063 |
2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-86+9534A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38905383 | |||||||
| chr2:38905538 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-86+9689C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38905538 | |||||||
| chr2:38905926 | G | C | 20 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0003g0242 others(17): Show |
20 | HG01106.hp2 HG01884.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.-86+10077G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38905926 | |||||||
| chr2:38905986 | G | A | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-86+10137G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38905986 | |||||||
| chr2:38906109 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-86+10260T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906109 | |||||||
| chr2:38906151 | C | T | 5 | a0001c0001t0003g0209 a0001c0001t0004g0266 a0001c0001t0004g0267 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+10302C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906151 | |||||||
| chr2:38906188 | C | CA | 30 | a0001c0001t0001g0073 a0001c0001t0001g0103 a0001c0001t0001g0104 others(27): Show |
30 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-86+10357dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38906188 | ||||||
| chr2:38906188 | C | CAA | 8 | a0001c0001t0001g0083 a0001c0001t0005g0010 a0001c0001t0005g0012 others(5): Show |
8 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-86+10356_-86+1035 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38906188 | ||||||
| chr2:38906262 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-86+10413T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906262 | |||||||
| chr2:38906306 | T | G | 1 | a0001c0001t0002g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-86+10457T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906306 | |||||||
| chr2:38906543 | G | A | 2 | a0001c0001t0003g0209 a0007c0011t0016g0210 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-86+10694G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906543 | |||||||
| chr2:38906683 | C | T | 5 | a0001c0001t0003g0209 a0001c0001t0004g0266 a0001c0001t0004g0267 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+10834C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906683 | |||||||
| chr2:38906713 | A | T | 16 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(13): Show |
16 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-86+10864A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906713 | |||||||
| chr2:38906749 | G | A | 1 | a0001c0001t0003g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-86+10900G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906749 | |||||||
| chr2:38906805 | C | CA | 26 | a0001c0001t0001g0112 a0001c0001t0002g0055 a0001c0001t0002g0269 others(23): Show |
27 | HG01361.hp2 HG01891.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.-86+10976dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38906805 | ||||||
| chr2:38906805 | CA | C | 20 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(17): Show |
20 | HG00323.hp1 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.-86+10976delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38906805 | ||||||
| chr2:38906827 | G | A | 1 | a0001c0001t0003g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-86+10978G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906827 | |||||||
| chr2:38906880 | C | A | 1 | a0001c0001t0018g0011 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-86+11031C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906880 | |||||||
| chr2:38906986 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(204): Show |
211 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.-86+11137T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38906986 | |||||||
| chr2:38907224 | A | G | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-86+11375A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907224 | |||||||
| chr2:38907248 | C | T | 16 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(13): Show |
16 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-86+11399C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907248 | |||||||
| chr2:38907254 | C | G | 1 | a0002c0002t0008g0197 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-86+11405C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907254 | |||||||
| chr2:38907297 | T | G | 34 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0003g0220 others(31): Show |
34 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.-86+11448T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907297 | |||||||
| chr2:38907860 | A | AT | 11 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0002g0060 others(8): Show |
11 | HG01981.hp2 HG02109.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.-85-11486dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38907860 | ||||||
| chr2:38907861 | T | TA | 7 | a0001c0001t0004g0208 a0001c0001t0004g0263 a0001c0001t0004g0264 others(4): Show |
7 | NA18949.hp1 NA18961.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-11502_-85-1150 others(5): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907861 | |||||||
| chr2:38907949 | C | G | 3 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-85-11414C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907949 | |||||||
| chr2:38907981 | C | T | 16 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(13): Show |
16 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-85-11382C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907981 | |||||||
| chr2:38907986 | C | T | 17 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0004g0208 others(14): Show |
18 | HG01361.hp2 HG02280.hp1 HG02818.hp1 others(15): Show |
intron_variant | MODIFIER | c.-85-11377C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38907986 | |||||||
| chr2:38908079 | G | A | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-11284G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908079 | |||||||
| chr2:38908140 | A | G | 1 | a0001c0001t0002g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-85-11223A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908140 | |||||||
| chr2:38908208 | G | T | 3 | a0001c0001t0001g0195 a0002c0002t0001g0096 a0002c0002t0001g0198 |
3 | NA18986.hp1 NA19068.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-85-11155G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908208 | |||||||
| chr2:38908289 | C | G | 2 | a0001c0001t0004g0264 a0001c0001t0004g0265 |
2 | NA18963.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-85-11074C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908289 | |||||||
| chr2:38908358 | T | G | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-11005T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908358 | |||||||
| chr2:38908367 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0167 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-85-10996A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908367 | |||||||
| chr2:38908397 | T | G | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0009g0005 |
4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-10966T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908397 | |||||||
| chr2:38908536 | C | G | 12 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(9): Show |
12 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-85-10827C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908536 | |||||||
| chr2:38908569 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-85-10794T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908569 | |||||||
| chr2:38908707 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-85-10656C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908707 | |||||||
| chr2:38908781 | G | T | 12 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(9): Show |
12 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-85-10582G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908781 | |||||||
| chr2:38908786 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(151): Show |
157 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.-85-10577T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38908786 | |||||||
| chr2:38909184 | T | C | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG01074.hp2 HG01123.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-10179T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909184 | |||||||
| chr2:38909465 | T | C | 2 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-85-9898T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909465 | |||||||
| chr2:38909492 | CT | C | 10 | a0001c0001t0001g0095 a0001c0001t0001g0123 a0001c0001t0001g0124 others(7): Show |
10 | HG01168.hp2 HG01943.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-85-9853delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38909492 | ||||||
| chr2:38909494 | T | C | 1 | a0001c0001t0004g0263 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-85-9869T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909494 | |||||||
| chr2:38909560 | A | C | 1 | a0001c0001t0001g0169 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-85-9803A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909560 | |||||||
| chr2:38909705 | GAT | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0164 others(3): Show |
7 | HG00738.hp2 HG01891.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-9657_-85-9656d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909705 | |||||||
| chr2:38909706 | A | AT | 5 | a0001c0001t0002g0018 a0001c0001t0002g0236 a0001c0001t0002g0269 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-9638dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38909706 | ||||||
| chr2:38909706 | AT | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(169): Show |
174 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.-85-9638delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38909706 | ||||||
| chr2:38909706 | ATT | A | 19 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(16): Show |
19 | HG01070.hp2 HG01074.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.-85-9639_-85-9638d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38909706 | ||||||
| chr2:38909969 | C | T | 1 | a0001c0001t0003g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-85-9394C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909969 | |||||||
| chr2:38909975 | G | GTTAT | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-85-9385_-85-9382d others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38909975 | ||||||
| chr2:38909982 | T | A | 5 | a0001c0001t0003g0209 a0001c0001t0004g0266 a0001c0001t0004g0267 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-9381T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38909982 | |||||||
| chr2:38910129 | C | G | 2 | a0001c0001t0003g0209 a0007c0011t0016g0210 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-85-9234C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38910129 | |||||||
| chr2:38910411 | A | C | 1 | a0001c0001t0002g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-85-8952A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38910411 | |||||||
| chr2:38910434 | G | C | 16 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(13): Show |
16 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-85-8929G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38910434 | |||||||
| chr2:38910830 | C | G | 1 | a0001c0001t0005g0010 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-85-8533C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38910830 | |||||||
| chr2:38911041 | C | T | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-8322C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911041 | |||||||
| chr2:38911051 | A | C | 1 | a0001c0001t0001g0163 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-85-8312A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911051 | |||||||
| chr2:38911341 | A | C | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-85-8022A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911341 | |||||||
| chr2:38911500 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(202): Show |
209 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.-85-7863A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911500 | |||||||
| chr2:38911517 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-85-7846C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911517 | |||||||
| chr2:38911566 | A | G | 2 | a0001c0001t0003g0220 a0001c0001t0003g0224 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-85-7797A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911566 | |||||||
| chr2:38911753 | G | A | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0009g0005 |
4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-7610G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911753 | |||||||
| chr2:38911806 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-85-7557G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911806 | |||||||
| chr2:38911955 | G | T | 6 | a0001c0001t0006g0239 a0001c0001t0006g0254 a0001c0001t0006g0255 others(3): Show |
6 | NA18952.hp2 NA18956.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-7408G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911955 | |||||||
| chr2:38911959 | G | C | 1 | a0001c0001t0003g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-7404G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38911959 | |||||||
| chr2:38912068 | C | T | 2 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-85-7295C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912068 | |||||||
| chr2:38912101 | A | G | 8 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(5): Show |
8 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-85-7262A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912101 | |||||||
| chr2:38912135 | C | T | 2 | a0001c0001t0003g0246 a0001c0001t0003g0247 |
2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-85-7228C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912135 | |||||||
| chr2:38912168 | G | A | 1 | a0001c0001t0005g0012 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-85-7195G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912168 | |||||||
| chr2:38912360 | G | A | 1 | a0002c0002t0001g0179 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-85-7003G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912360 | |||||||
| chr2:38912375 | G | A | 4 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-6988G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912375 | |||||||
| chr2:38912376 | A | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(4): Show |
7 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-6987A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912376 | |||||||
| chr2:38912403 | C | G | 13 | a0001c0001t0002g0223 a0001c0001t0003g0220 a0001c0001t0003g0221 others(10): Show |
13 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-85-6960C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912403 | |||||||
| chr2:38912640 | G | A | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-85-6723G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912640 | |||||||
| chr2:38912735 | A | G | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-6628A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912735 | |||||||
| chr2:38912775 | C | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(124): Show |
130 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.-85-6588C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912775 | |||||||
| chr2:38912784 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-85-6579A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912784 | |||||||
| chr2:38912877 | C | T | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-85-6486C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912877 | |||||||
| chr2:38912967 | G | C | 5 | a0001c0001t0003g0209 a0001c0001t0004g0266 a0001c0001t0004g0267 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-6396G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38912967 | |||||||
| chr2:38913038 | G | GT | 11 | a0001c0001t0001g0127 a0001c0001t0001g0162 a0001c0001t0002g0052 others(8): Show |
11 | HG02922.hp1 HG03471.hp2 HG03942.hp1 others(8): Show |
intron_variant | MODIFIER | c.-85-6309dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38913038 | ||||||
| chr2:38913038 | G | GTT | 17 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(14): Show |
17 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-85-6310_-85-6309d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38913038 | ||||||
| chr2:38913216 | G | C | 10 | a0001c0001t0006g0239 a0001c0001t0006g0250 a0001c0001t0006g0251 others(7): Show |
10 | HG01106.hp2 HG01993.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.-85-6147G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38913216 | |||||||
| chr2:38913474 | A | G | 2 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-85-5889A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38913474 | |||||||
| chr2:38913744 | G | A | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-85-5619G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38913744 | |||||||
| chr2:38913973 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(151): Show |
157 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.-85-5390C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38913973 | |||||||
| chr2:38913984 | A | G | 1 | a0001c0001t0005g0061 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-85-5379A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38913984 | |||||||
| chr2:38913988 | T | G | 1 | a0001c0001t0003g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85-5375T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38913988 | |||||||
| chr2:38914127 | G | T | 1 | a0001c0001t0001g0161 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-85-5236G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914127 | |||||||
| chr2:38914165 | T | G | 1 | a0001c0001t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-85-5198T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914165 | |||||||
| chr2:38914226 | A | G | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-85-5137A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914226 | |||||||
| chr2:38914405 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-85-4958C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914405 | |||||||
| chr2:38914431 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-85-4932G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914431 | |||||||
| chr2:38914465 | C | G | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-85-4898C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914465 | |||||||
| chr2:38914530 | G | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0160 |
2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-85-4833G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914530 | |||||||
| chr2:38914599 | G | A | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-85-4764G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914599 | |||||||
| chr2:38914628 | C | G | 1 | a0004c0006t0001g0102 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-85-4735C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914628 | |||||||
| chr2:38914643 | G | T | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG01074.hp2 HG01123.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-4720G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914643 | |||||||
| chr2:38914664 | CA | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(176): Show |
182 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(179): Show |
intron_variant | MODIFIER | c.-85-4679delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38914664 | ||||||
| chr2:38914725 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-85-4638C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38914725 | |||||||
| chr2:38915188 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-85-4175C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915188 | |||||||
| chr2:38915318 | G | A | 2 | a0001c0003t0002g0271 a0001c0003t0002g0272 |
2 | NA18991.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-85-4045G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915318 | |||||||
| chr2:38915371 | T | C | 3 | a0002c0002t0001g0179 a0002c0002t0001g0180 a0002c0002t0001g0181 |
3 | HG02602.hp2 HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-85-3992T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915371 | |||||||
| chr2:38915382 | C | CT | 26 | a0001c0001t0002g0070 a0001c0001t0002g0236 a0001c0001t0003g0240 others(23): Show |
26 | HG01106.hp2 HG01361.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.-85-3961dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38915382 | ||||||
| chr2:38915382 | C | CTT | 29 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0003g0209 others(26): Show |
29 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.-85-3962_-85-3961d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38915382 | ||||||
| chr2:38915382 | CT | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(127): Show |
133 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.-85-3961delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38915382 | ||||||
| chr2:38915382 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-85-3970_-85-3961d others(12): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38915382 | ||||||
| chr2:38915459 | A | G | 4 | a0001c0001t0004g0208 a0001c0003t0004g0204 a0001c0003t0004g0205 others(1): Show |
4 | NA18949.hp1 NA18988.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-3904A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915459 | |||||||
| chr2:38915518 | G | A | 13 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(10): Show |
13 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-85-3845G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915518 | |||||||
| chr2:38915684 | T | G | 5 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0009g0005 others(2): Show |
6 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-3679T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915684 | |||||||
| chr2:38915915 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0160 |
2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-85-3448G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915915 | |||||||
| chr2:38915916 | C | G | 15 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(12): Show |
15 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-85-3447C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38915916 | |||||||
| chr2:38916212 | C | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(128): Show |
134 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.-85-3151C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916212 | |||||||
| chr2:38916232 | A | T | 16 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(13): Show |
16 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-85-3131A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916232 | |||||||
| chr2:38916266 | C | A | 18 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(15): Show |
18 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-85-3097C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916266 | |||||||
| chr2:38916297 | G | A | 18 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(15): Show |
18 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-85-3066G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916297 | |||||||
| chr2:38916500 | G | A | 1 | a0001c0001t0003g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-85-2863G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916500 | |||||||
| chr2:38916533 | G | T | 1 | a0001c0001t0003g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-85-2830G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916533 | |||||||
| chr2:38916573 | C | G | 13 | a0001c0001t0002g0223 a0001c0001t0003g0220 a0001c0001t0003g0221 others(10): Show |
13 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-85-2790C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916573 | |||||||
| chr2:38916662 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(136): Show |
142 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-85-2701T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916662 | |||||||
| chr2:38916801 | C | CT | 27 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0003g0220 others(24): Show |
27 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.-85-2546dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38916801 | ||||||
| chr2:38916801 | C | CTT | 11 | a0001c0001t0003g0209 a0001c0001t0004g0208 a0001c0001t0004g0263 others(8): Show |
11 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.-85-2547_-85-2546d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38916801 | ||||||
| chr2:38916875 | ACTGCAAC others(2): Show |
A | 3 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-85-2483_-85-2475d others(11): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38916875 | ||||||
| chr2:38916950 | G | A | 4 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0004g0261 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-2413G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916950 | |||||||
| chr2:38916957 | C | T | 12 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0004g0211 others(9): Show |
13 | HG01361.hp2 HG02280.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.-85-2406C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916957 | |||||||
| chr2:38916958 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-85-2405G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916958 | |||||||
| chr2:38916967 | A | C | 22 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0003g0220 others(19): Show |
22 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-85-2396A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38916967 | |||||||
| chr2:38917102 | C | CTTTTTTT others(4): Show |
11 | a0001c0001t0003g0209 a0001c0001t0004g0263 a0001c0001t0004g0264 others(8): Show |
11 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.-85-2254_-85-2253i others(13): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917102 | ||||||
| chr2:38917102 | C | CTTTTTTT others(5): Show |
12 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0004g0208 others(9): Show |
13 | HG01361.hp2 HG01993.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-85-2254_-85-2253i others(14): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917102 | ||||||
| chr2:38917102 | C | CTTTTTTT others(6): Show |
37 | a0001c0001t0001g0112 a0001c0001t0002g0222 a0001c0001t0002g0223 others(34): Show |
37 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.-85-2254_-85-2253i others(15): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917102 | ||||||
| chr2:38917102 | C | CTTTTTTT others(7): Show |
146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(143): Show |
149 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.-85-2254_-85-2253i others(16): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917102 | ||||||
| chr2:38917102 | C | CTTTTTTT others(8): Show |
6 | a0001c0001t0001g0101 a0001c0001t0001g0114 a0001c0001t0001g0202 others(3): Show |
6 | HG01109.hp1 HG03209.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-2254_-85-2253i others(17): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917102 | ||||||
| chr2:38917102 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0005g0010 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-85-2254_-85-2253i others(18): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917102 | ||||||
| chr2:38917389 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0158 |
2 | HG01192.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-85-1974G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38917389 | |||||||
| chr2:38917433 | T | C | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-85-1930T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38917433 | |||||||
| chr2:38917552 | A | G | 3 | a0001c0001t0001g0097 a0001c0001t0001g0157 a0001c0001t0005g0156 |
3 | HG03041.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-85-1811A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38917552 | |||||||
| chr2:38917686 | A | C | 2 | a0002c0002t0005g0067 a0002c0002t0005g0068 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-85-1677A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38917686 | |||||||
| chr2:38917828 | C | CA | 8 | a0001c0001t0001g0123 a0001c0001t0001g0130 a0001c0001t0001g0158 others(5): Show |
8 | HG01192.hp1 HG01978.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.-85-1516dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917828 | ||||||
| chr2:38917828 | CA | C | 7 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0002g0223 others(4): Show |
7 | HG01243.hp2 HG01361.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85-1516delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38917828 | ||||||
| chr2:38918065 | G | A | 10 | a0001c0001t0004g0208 a0001c0001t0004g0263 a0001c0001t0004g0264 others(7): Show |
10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-85-1298G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918065 | |||||||
| chr2:38918078 | T | C | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-85-1285T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918078 | |||||||
| chr2:38918145 | T | C | 12 | a0001c0001t0003g0209 a0001c0001t0004g0208 a0001c0001t0004g0263 others(9): Show |
12 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.-85-1218T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918145 | |||||||
| chr2:38918193 | C | T | 3 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0010g0213 |
3 | HG01361.hp2 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-85-1170C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918193 | |||||||
| chr2:38918372 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-85-991G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918372 | |||||||
| chr2:38918643 | C | T | 44 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0269 others(41): Show |
45 | HG01106.hp2 HG01243.hp2 HG01361.hp2 others(42): Show |
intron_variant | MODIFIER | c.-85-720C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918643 | |||||||
| chr2:38918877 | C | CA | 48 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(45): Show |
49 | HG00609.hp2 HG00741.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.-85-468dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38918877 | ||||||
| chr2:38918877 | C | CAA | 9 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0133 others(6): Show |
9 | HG01361.hp2 HG01433.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.-85-469_-85-468dup others(2): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 38918877 | ||||||
| chr2:38918984 | G | A | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-85-379G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38918984 | |||||||
| chr2:38919166 | T | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0139 |
2 | HG01943.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-85-197T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38919166 | |||||||
| chr2:38919167 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0139 |
2 | HG01943.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-85-196G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38919167 | |||||||
| chr2:38919259 | A | T | 1 | a0001c0001t0003g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-85-104A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38919259 | |||||||
| chr2:38919309 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-85-54C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38919309 | |||||||
| chr2:38919348 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-85-15G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38919348 | |||||||
| chr2:38919349 | A | C | 10 | a0001c0001t0014g0094 a0002c0002t0001g0089 a0002c0002t0001g0174 others(7): Show |
10 | HG00597.hp2 HG02165.hp2 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.-85-14A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | chr2 | 38919349 | |||||||
| chr2:38919599 | T | C | 8 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0003g0242 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+127T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38919599 | |||||||
| chr2:38919830 | A | G | 40 | a0001c0001t0001g0079 a0001c0001t0001g0178 a0001c0001t0001g0183 others(37): Show |
40 | HG00597.hp2 HG01123.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.25+358A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38919830 | |||||||
| chr2:38920109 | C | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(205): Show |
212 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.25+637C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920109 | |||||||
| chr2:38920175 | C | T | 2 | a0001c0001t0003g0209 a0007c0011t0016g0210 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.25+703C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920175 | |||||||
| chr2:38920199 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.25+727A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920199 | |||||||
| chr2:38920398 | C | CT | 9 | a0001c0001t0002g0007 a0001c0001t0002g0021 a0001c0001t0002g0023 others(6): Show |
9 | HG00741.hp2 HG01106.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-950dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 38920398 | ||||||
| chr2:38920398 | CT | C | 7 | a0001c0001t0002g0008 a0001c0001t0002g0035 a0001c0001t0002g0053 others(4): Show |
7 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-950delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 38920398 | ||||||
| chr2:38920398 | CTT | C | 21 | a0001c0001t0001g0079 a0001c0001t0001g0103 a0001c0001t0001g0121 others(18): Show |
21 | HG01123.hp1 HG01361.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+951_26-950delTT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 38920398 | ||||||
| chr2:38920398 | CTTT | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(167): Show |
173 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.25+950_26-950delTT others(1): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 38920398 | ||||||
| chr2:38920398 | CTTTT | C | 9 | a0001c0001t0001g0141 a0001c0001t0001g0157 a0001c0001t0002g0269 others(6): Show |
10 | HG01257.hp1 HG01258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+949_26-950delTT others(2): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 38920398 | ||||||
| chr2:38920499 | C | T | 3 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0062 |
3 | HG03654.hp1 HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.26-875C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920499 | |||||||
| chr2:38920510 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | NA18945.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.26-864C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920510 | |||||||
| chr2:38920820 | C | T | 2 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.26-554C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920820 | |||||||
| chr2:38920832 | C | CT | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.26-538dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 38920832 | ||||||
| chr2:38920964 | G | A | 2 | a0002c0002t0001g0175 a0002c0002t0001g0177 |
2 | HG00597.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.26-410G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38920964 | |||||||
| chr2:38921143 | G | A | 3 | a0001c0001t0002g0223 a0001c0001t0003g0227 a0001c0001t0003g0237 |
3 | HG01243.hp2 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.26-231G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38921143 | |||||||
| chr2:38921252 | G | A | 39 | a0001c0001t0001g0079 a0001c0001t0001g0178 a0001c0001t0001g0183 others(36): Show |
39 | HG00597.hp2 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.26-122G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 3/17 | chr2 | 38921252 | |||||||
| chr2:38922017 | A | G | 1 | a0001c0001t0002g0016 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.75+594A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922017 | |||||||
| chr2:38922075 | A | G | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75+652A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922075 | |||||||
| chr2:38922077 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.75+654T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922077 | |||||||
| chr2:38922148 | T | C | 12 | a0001c0001t0003g0209 a0001c0001t0004g0208 a0001c0001t0004g0263 others(9): Show |
12 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+725T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922148 | |||||||
| chr2:38922266 | C | A | 34 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0003g0220 others(31): Show |
34 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.75+843C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922266 | |||||||
| chr2:38922342 | G | T | 34 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0003g0220 others(31): Show |
34 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.75+919G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922342 | |||||||
| chr2:38922430 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.75+1007A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922430 | |||||||
| chr2:38922637 | T | G | 2 | a0001c0003t0002g0271 a0001c0003t0002g0272 |
2 | NA18991.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.75+1214T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922637 | |||||||
| chr2:38922642 | C | T | 11 | a0001c0001t0003g0209 a0001c0001t0004g0263 a0001c0001t0004g0264 others(8): Show |
11 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+1219C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922642 | |||||||
| chr2:38922754 | C | T | 8 | a0001c0001t0001g0178 a0001c0001t0001g0195 a0002c0002t0001g0096 others(5): Show |
8 | NA18942.hp1 NA18953.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+1331C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922754 | |||||||
| chr2:38922770 | A | C | 12 | a0001c0001t0003g0209 a0001c0001t0004g0208 a0001c0001t0004g0263 others(9): Show |
12 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+1347A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922770 | |||||||
| chr2:38922918 | T | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(202): Show |
209 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.75+1495T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922918 | |||||||
| chr2:38922934 | C | A | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.75+1511C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38922934 | |||||||
| chr2:38923150 | A | G | 12 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(9): Show |
12 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+1727A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923150 | |||||||
| chr2:38923180 | A | G | 3 | a0001c0001t0001g0097 a0001c0001t0001g0157 a0001c0001t0005g0156 |
3 | HG03041.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.75+1757A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923180 | |||||||
| chr2:38923410 | A | T | 1 | a0010c0009t0001g0128 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.75+1987A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923410 | |||||||
| chr2:38923484 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(203): Show |
210 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.75+2061T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923484 | |||||||
| chr2:38923518 | T | C | 18 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(15): Show |
18 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.75+2095T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923518 | |||||||
| chr2:38923713 | A | G | 2 | a0001c0003t0002g0271 a0001c0003t0002g0272 |
2 | NA18991.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.75+2290A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923713 | |||||||
| chr2:38923760 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0072 others(141): Show |
147 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.75+2337T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38923760 | |||||||
| chr2:38924048 | A | T | 1 | a0001c0001t0002g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.75+2625A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924048 | |||||||
| chr2:38924053 | A | C | 1 | a0001c0001t0002g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.75+2630A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924053 | |||||||
| chr2:38924056 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.75+2633G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924056 | |||||||
| chr2:38924166 | A | C | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.75+2743A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924166 | |||||||
| chr2:38924352 | C | T | 2 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.75+2929C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924352 | |||||||
| chr2:38924691 | G | C | 15 | a0001c0001t0003g0209 a0001c0001t0004g0263 a0001c0001t0004g0264 others(12): Show |
15 | HG02572.hp2 HG02615.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+3268G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924691 | |||||||
| chr2:38924720 | T | G | 1 | a0002c0002t0001g0176 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.75+3297T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924720 | |||||||
| chr2:38924942 | A | C | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.75+3519A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38924942 | |||||||
| chr2:38925080 | AAGAG | A | 6 | a0001c0001t0001g0195 a0002c0002t0001g0096 a0002c0002t0001g0187 others(3): Show |
6 | NA18953.hp1 NA18955.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+3660_75+3663del others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 38925080 | ||||||
| chr2:38925124 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.75+3701T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925124 | |||||||
| chr2:38925389 | G | C | 33 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0003g0220 others(30): Show |
33 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.76-3518G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925389 | |||||||
| chr2:38925393 | A | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(253): Show |
260 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(257): Show |
intron_variant | MODIFIER | c.76-3514A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925393 | |||||||
| chr2:38925397 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.76-3510C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925397 | |||||||
| chr2:38925518 | A | G | 6 | a0001c0001t0003g0209 a0001c0004t0004g0075 a0001c0004t0004g0076 others(3): Show |
6 | HG02615.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-3389A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925518 | |||||||
| chr2:38925547 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.76-3360G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925547 | |||||||
| chr2:38925561 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-3346T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925561 | |||||||
| chr2:38925646 | A | G | 2 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.76-3261A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38925646 | |||||||
| chr2:38926011 | C | A | 2 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.76-2896C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38926011 | |||||||
| chr2:38926491 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.76-2416G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38926491 | |||||||
| chr2:38927101 | T | C | 16 | a0001c0001t0003g0209 a0001c0001t0004g0208 a0001c0001t0004g0263 others(13): Show |
16 | HG02572.hp2 HG02615.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.76-1806T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927101 | |||||||
| chr2:38927124 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.76-1783C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927124 | |||||||
| chr2:38927322 | T | G | 131 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0001g0103 others(128): Show |
133 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(130): Show |
intron_variant | MODIFIER | c.76-1585T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927322 | |||||||
| chr2:38927418 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.76-1489G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927418 | |||||||
| chr2:38927523 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.76-1384C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927523 | |||||||
| chr2:38927525 | G | A | 33 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0003g0220 others(30): Show |
33 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.76-1382G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927525 | |||||||
| chr2:38927644 | C | T | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.76-1263C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927644 | |||||||
| chr2:38927674 | C | T | 3 | a0002c0002t0001g0174 a0002c0002t0001g0199 a0002c0002t0001g0200 |
3 | NA18977.hp1 NA19065.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.76-1233C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927674 | |||||||
| chr2:38927791 | C | T | 6 | a0001c0001t0002g0223 a0001c0001t0003g0227 a0001c0001t0003g0229 others(3): Show |
6 | HG01243.hp2 HG02615.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-1116C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927791 | |||||||
| chr2:38927911 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.76-996A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927911 | |||||||
| chr2:38927952 | T | C | 1 | a0001c0001t0002g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.76-955T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927952 | |||||||
| chr2:38927953 | T | C | 2 | a0001c0001t0002g0269 a0001c0001t0009g0005 |
3 | HG02280.hp1 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.76-954T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927953 | |||||||
| chr2:38927993 | C | T | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.76-914C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38927993 | |||||||
| chr2:38928023 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.76-884C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928023 | |||||||
| chr2:38928024 | G | T | 1 | a0001c0001t0002g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.76-883G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928024 | |||||||
| chr2:38928110 | T | C | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.76-797T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928110 | |||||||
| chr2:38928125 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-782A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928125 | |||||||
| chr2:38928364 | T | G | 1 | a0001c0001t0003g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.76-543T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928364 | |||||||
| chr2:38928399 | T | A | 6 | a0001c0001t0004g0208 a0001c0004t0004g0075 a0001c0004t0004g0076 others(3): Show |
6 | HG02615.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-508T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928399 | |||||||
| chr2:38928399 | T | TA | 8 | a0001c0001t0004g0263 a0001c0001t0004g0264 a0001c0001t0004g0265 others(5): Show |
8 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-500dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 38928399 | ||||||
| chr2:38928565 | G | A | 9 | a0001c0001t0004g0208 a0001c0001t0004g0263 a0001c0001t0004g0264 others(6): Show |
9 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-342G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928565 | |||||||
| chr2:38928591 | T | A | 2 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.76-316T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928591 | |||||||
| chr2:38928684 | A | AT | 11 | a0001c0001t0003g0209 a0001c0001t0004g0208 a0001c0001t0004g0263 others(8): Show |
11 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-220dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 38928684 | ||||||
| chr2:38928855 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.76-52C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 4/17 | chr2 | 38928855 | |||||||
| chr2:38929196 | C | T | 9 | a0001c0001t0004g0263 a0001c0001t0004g0264 a0001c0001t0004g0265 others(6): Show |
9 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+125C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | chr2 | 38929196 | |||||||
| chr2:38929257 | C | T | 1 | a0001c0001t0002g0016 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.240+186C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | chr2 | 38929257 | |||||||
| chr2:38929283 | G | T | 1 | a0001c0001t0003g0230 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.240+212G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | chr2 | 38929283 | |||||||
| chr2:38929301 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.240+230C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | chr2 | 38929301 | |||||||
| chr2:38929591 | C | CTCAT | 10 | a0001c0001t0004g0208 a0001c0001t0004g0263 a0001c0001t0004g0264 others(7): Show |
10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-98_241-95dupTT others(2): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 38929591 | ||||||
| chr2:38929665 | T | C | 3 | a0001c0001t0001g0171 a0001c0001t0002g0035 a0001c0001t0002g0045 |
3 | HG01099.hp2 HG01516.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.241-44T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | chr2 | 38929665 | |||||||
| chr2:38929680 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.241-29G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 5/17 | chr2 | 38929680 | |||||||
| chr2:38929920 | A | G | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.362+90A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38929920 | |||||||
| chr2:38930022 | A | G | 4 | a0001c0001t0003g0241 a0001c0001t0004g0211 a0001c0001t0004g0212 others(1): Show |
4 | HG01361.hp2 HG02886.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.362+192A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930022 | |||||||
| chr2:38930189 | T | C | 32 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0003g0220 others(29): Show |
32 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.362+359T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930189 | |||||||
| chr2:38930234 | A | G | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.362+404A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930234 | |||||||
| chr2:38930392 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.362+562C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930392 | |||||||
| chr2:38930393 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.362+563A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930393 | |||||||
| chr2:38930446 | C | G | 3 | a0003c0005t0001g0002 a0003c0005t0001g0140 a0003c0005t0012g0002 |
3 | HG01257.hp1 HG01258.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.362+616C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930446 | |||||||
| chr2:38930495 | G | A | 1 | a0001c0001t0004g0259 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.363-614G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930495 | |||||||
| chr2:38930588 | C | G | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.363-521C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930588 | |||||||
| chr2:38930951 | T | C | 1 | a0002c0002t0001g0182 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.363-158T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 6/17 | chr2 | 38930951 | |||||||
| chr2:38931412 | A | T | 6 | a0001c0001t0001g0195 a0002c0002t0001g0096 a0002c0002t0001g0187 others(3): Show |
6 | NA18953.hp1 NA18955.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.505+161A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38931412 | |||||||
| chr2:38931439 | A | AT | 8 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0153 others(5): Show |
8 | HG02723.hp2 HG03471.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.505+198dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38931439 | ||||||
| chr2:38931461 | G | A | 7 | a0001c0001t0001g0134 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG00558.hp2 HG02165.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.505+210G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38931461 | |||||||
| chr2:38931605 | C | G | 13 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(10): Show |
13 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.505+354C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38931605 | |||||||
| chr2:38931809 | CTTTGTAT others(11): Show |
C | 1 | a0001c0001t0004g0208 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.505+560_505+577del others(18): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38931809 | ||||||
| chr2:38932191 | C | T | 1 | a0002c0002t0001g0082 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.505+940C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38932191 | |||||||
| chr2:38932442 | AT | A | 124 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0002g0004 others(121): Show |
126 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(123): Show |
intron_variant | MODIFIER | c.505+1201delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38932442 | ||||||
| chr2:38932443 | T | G | 2 | a0001c0001t0003g0209 a0007c0011t0016g0210 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.505+1192T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38932443 | |||||||
| chr2:38932444 | T | G | 10 | a0001c0001t0004g0208 a0001c0001t0004g0263 a0001c0001t0004g0264 others(7): Show |
10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.505+1193T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38932444 | |||||||
| chr2:38932457 | A | G | 1 | a0002c0002t0001g0192 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.505+1206A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38932457 | |||||||
| chr2:38932475 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0133 |
2 | HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.505+1224G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38932475 | |||||||
| chr2:38932626 | T | G | 1 | a0001c0014t0002g0056 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.505+1375T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38932626 | |||||||
| chr2:38933382 | G | GT | 9 | a0001c0001t0001g0112 a0001c0001t0001g0126 a0001c0001t0002g0055 others(6): Show |
9 | HG02615.hp1 NA18949.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.505+2141dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38933382 | ||||||
| chr2:38933447 | G | T | 12 | a0001c0001t0003g0209 a0001c0001t0004g0208 a0001c0001t0004g0263 others(9): Show |
12 | HG02572.hp2 HG02723.hp2 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.505+2196G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933447 | |||||||
| chr2:38933453 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.505+2202G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933453 | |||||||
| chr2:38933488 | G | A | 123 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0002g0004 others(120): Show |
125 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(122): Show |
intron_variant | MODIFIER | c.505+2237G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933488 | |||||||
| chr2:38933709 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | NA18945.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.506-2066A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933709 | |||||||
| chr2:38933890 | C | T | 13 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0003g0220 others(10): Show |
13 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.506-1885C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933890 | |||||||
| chr2:38933944 | A | T | 1 | a0010c0009t0001g0128 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.506-1831A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933944 | |||||||
| chr2:38933996 | T | C | 3 | a0001c0001t0003g0209 a0007c0011t0016g0210 a0011c0008t0004g0214 |
3 | HG02723.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.506-1779T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38933996 | |||||||
| chr2:38934047 | T | C | 3 | a0001c0001t0002g0037 a0001c0001t0003g0209 a0007c0011t0016g0210 |
3 | HG01256.hp1 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.506-1728T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934047 | |||||||
| chr2:38934063 | T | C | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.506-1712T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934063 | |||||||
| chr2:38934095 | G | A | 1 | a0002c0002t0001g0176 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.506-1680G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934095 | |||||||
| chr2:38934109 | A | T | 10 | a0001c0001t0004g0208 a0001c0001t0004g0263 a0001c0001t0004g0264 others(7): Show |
10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.506-1666A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934109 | |||||||
| chr2:38934222 | T | A | 2 | a0001c0001t0003g0209 a0007c0011t0016g0210 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.506-1553T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934222 | |||||||
| chr2:38934449 | C | T | 1 | a0002c0002t0001g0192 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.506-1326C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934449 | |||||||
| chr2:38934497 | A | ATCCCTCC others(12): Show |
7 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0004g0259 others(4): Show |
7 | HG01361.hp2 HG02818.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.506-1246_506-1228d others(21): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934497 | ||||||
| chr2:38934497 | ATCCCTCC others(12): Show |
A | 19 | a0001c0001t0003g0240 a0001c0001t0003g0242 a0001c0001t0003g0243 others(16): Show |
19 | HG01106.hp2 HG01884.hp2 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.506-1246_506-1228d others(21): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934497 | ||||||
| chr2:38934515 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0133 |
2 | HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.506-1260C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934515 | |||||||
| chr2:38934537 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0159 |
2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.506-1238C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934537 | |||||||
| chr2:38934548 | T | C | 10 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0003g0241 others(7): Show |
11 | HG02280.hp1 HG02615.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.506-1227T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934548 | |||||||
| chr2:38934556 | T | C | 10 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0003g0241 others(7): Show |
11 | HG02280.hp1 HG02615.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.506-1219T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934556 | |||||||
| chr2:38934557 | C | CCTCCCCC others(42): Show |
9 | a0001c0001t0002g0269 a0001c0001t0003g0241 a0001c0001t0009g0005 others(6): Show |
10 | HG02280.hp1 HG02615.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.506-1213_506-1212i others(51): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934557 | ||||||
| chr2:38934557 | C | CCTCCCCC others(102): Show |
1 | a0001c0001t0002g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.506-1213_506-1212i others(111): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934557 | ||||||
| chr2:38934557 | C | CCTCCCGC others(24): Show |
7 | a0001c0001t0002g0023 a0001c0001t0002g0062 a0001c0001t0002g0223 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.506-1191_506-1190i others(33): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934557 | ||||||
| chr2:38934557 | C | CCTCCCGC others(23): Show |
88 | a0001c0001t0001g0066 a0001c0001t0001g0090 a0001c0001t0001g0091 others(85): Show |
89 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(86): Show |
intron_variant | MODIFIER | c.506-1122_506-1093d others(32): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934557 | ||||||
| chr2:38934557 | CCTCCCGC others(23): Show |
C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0003t0015g0173 |
3 | HG01069.hp1 HG01361.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.506-1122_506-1093d others(32): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934557 | ||||||
| chr2:38934578 | T | TCCCCCCC others(25): Show |
1 | a0001c0001t0003g0246 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.506-1191_506-1190i others(34): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934578 | ||||||
| chr2:38934589 | T | TCCCGCTT others(24): Show |
1 | a0001c0001t0002g0069 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.506-1183_506-1153d others(33): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934589 | ||||||
| chr2:38934608 | T | TCCCCCCT others(24): Show |
3 | a0001c0001t0002g0007 a0001c0001t0002g0232 a0001c0014t0002g0056 |
3 | HG02055.hp2 HG02809.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.506-1161_506-1131d others(33): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934608 | ||||||
| chr2:38934638 | T | TCCCCCCT others(24): Show |
1 | a0001c0001t0002g0006 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.506-1131_506-1101d others(33): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38934638 | ||||||
| chr2:38934653 | G | A | 7 | a0001c0001t0004g0208 a0001c0001t0004g0263 a0001c0001t0004g0264 others(4): Show |
7 | NA18949.hp1 NA18961.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.506-1122G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934653 | |||||||
| chr2:38934857 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.506-918T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934857 | |||||||
| chr2:38934951 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.506-824A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934951 | |||||||
| chr2:38934959 | G | A | 2 | a0002c0002t0005g0067 a0002c0002t0005g0068 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.506-816G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38934959 | |||||||
| chr2:38935003 | C | T | 67 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0002g0004 others(64): Show |
68 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.506-772C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935003 | |||||||
| chr2:38935011 | A | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.506-764A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935011 | |||||||
| chr2:38935048 | T | TA | 69 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0001g0101 others(66): Show |
70 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.506-712dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38935048 | ||||||
| chr2:38935048 | TA | T | 14 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(11): Show |
14 | HG01433.hp1 HG02572.hp2 HG03225.hp1 others(11): Show |
intron_variant | MODIFIER | c.506-712delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38935048 | ||||||
| chr2:38935076 | A | C | 2 | a0001c0001t0003g0209 a0007c0011t0016g0210 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.506-699A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935076 | |||||||
| chr2:38935149 | C | T | 67 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0002g0004 others(64): Show |
68 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.506-626C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935149 | |||||||
| chr2:38935245 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.506-530A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935245 | |||||||
| chr2:38935296 | T | C | 1 | a0001c0001t0002g0222 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.506-479T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935296 | |||||||
| chr2:38935342 | G | A | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.506-433G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935342 | |||||||
| chr2:38935644 | CT | C | 68 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0002g0004 others(65): Show |
69 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.506-123delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 38935644 | ||||||
| chr2:38935676 | C | G | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.506-99C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935676 | |||||||
| chr2:38935691 | C | G | 12 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(9): Show |
12 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.506-84C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | chr2 | 38935691 | |||||||
| chr2:38936019 | G | A | 3 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0010g0213 |
3 | HG01361.hp2 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.565+185G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936019 | |||||||
| chr2:38936036 | G | A | 10 | a0001c0001t0004g0208 a0001c0001t0004g0263 a0001c0001t0004g0264 others(7): Show |
10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+202G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936036 | |||||||
| chr2:38936068 | T | C | 140 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0001g0083 others(137): Show |
142 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(139): Show |
intron_variant | MODIFIER | c.565+234T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936068 | |||||||
| chr2:38936069 | T | C | 16 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(13): Show |
16 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+235T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936069 | |||||||
| chr2:38936092 | A | G | 1 | a0002c0002t0001g0191 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.565+258A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936092 | |||||||
| chr2:38936184 | C | G | 67 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0002g0004 others(64): Show |
68 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.565+350C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936184 | |||||||
| chr2:38936184 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.565+350C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936184 | |||||||
| chr2:38936188 | C | G | 1 | a0002c0002t0001g0190 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.565+354C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936188 | |||||||
| chr2:38936199 | G | A | 5 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0009g0005 others(2): Show |
6 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+365G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936199 | |||||||
| chr2:38936378 | C | T | 10 | a0001c0001t0004g0208 a0001c0001t0004g0263 a0001c0001t0004g0264 others(7): Show |
10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+544C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936378 | |||||||
| chr2:38936489 | A | G | 10 | a0001c0001t0004g0208 a0001c0001t0004g0263 a0001c0001t0004g0264 others(7): Show |
10 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+655A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936489 | |||||||
| chr2:38936646 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.566-689G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936646 | |||||||
| chr2:38936650 | A | G | 3 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0062 |
3 | HG03654.hp1 HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.566-685A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936650 | |||||||
| chr2:38936697 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | NA19070.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.566-638C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936697 | |||||||
| chr2:38936716 | C | G | 15 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(12): Show |
15 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-619C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936716 | |||||||
| chr2:38936860 | C | G | 1 | a0001c0001t0002g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.566-475C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936860 | |||||||
| chr2:38936875 | C | G | 12 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0103 others(9): Show |
12 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-460C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936875 | |||||||
| chr2:38936989 | G | A | 12 | a0001c0001t0002g0223 a0001c0001t0003g0220 a0001c0001t0003g0221 others(9): Show |
12 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-346G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38936989 | |||||||
| chr2:38936997 | C | CT | 8 | a0001c0001t0001g0079 a0001c0001t0002g0055 a0001c0001t0003g0230 others(5): Show |
8 | HG00741.hp2 HG02572.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-323dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 38936997 | ||||||
| chr2:38936997 | CT | C | 6 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0009g0005 others(3): Show |
7 | HG00738.hp1 HG02280.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-323delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 38936997 | ||||||
| chr2:38937051 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(218): Show |
225 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(222): Show |
intron_variant | MODIFIER | c.566-284A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937051 | |||||||
| chr2:38937055 | G | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(218): Show |
225 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(222): Show |
intron_variant | MODIFIER | c.566-280G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937055 | |||||||
| chr2:38937056 | G | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(218): Show |
225 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(222): Show |
intron_variant | MODIFIER | c.566-279G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937056 | |||||||
| chr2:38937058 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(216): Show |
223 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(220): Show |
intron_variant | MODIFIER | c.566-277G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937058 | |||||||
| chr2:38937074 | A | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(212): Show |
219 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(216): Show |
intron_variant | MODIFIER | c.566-261A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937074 | |||||||
| chr2:38937075 | A | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(212): Show |
219 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(216): Show |
intron_variant | MODIFIER | c.566-260A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937075 | |||||||
| chr2:38937087 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(220): Show |
227 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(224): Show |
intron_variant | MODIFIER | c.566-248T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937087 | |||||||
| chr2:38937089 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(220): Show |
227 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(224): Show |
intron_variant | MODIFIER | c.566-246G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937089 | |||||||
| chr2:38937098 | G | C | 133 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0001g0083 others(130): Show |
135 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(132): Show |
intron_variant | MODIFIER | c.566-237G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937098 | |||||||
| chr2:38937112 | A | G | 2 | a0001c0001t0003g0229 a0001c0001t0003g0248 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.566-223A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937112 | |||||||
| chr2:38937151 | C | T | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.566-184C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937151 | |||||||
| chr2:38937187 | G | C | 3 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | NA18948.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.566-148G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937187 | |||||||
| chr2:38937208 | A | G | 12 | a0001c0001t0003g0209 a0001c0001t0003g0249 a0001c0001t0006g0239 others(9): Show |
12 | HG01106.hp2 HG01993.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-127A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937208 | |||||||
| chr2:38937324 | C | A | 43 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0092 others(40): Show |
44 | HG01070.hp2 HG01106.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-11C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 8/17 | chr2 | 38937324 | |||||||
| chr2:38937643 | C | A | 2 | a0001c0001t0003g0248 a0007c0011t0016g0210 |
2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.790+84C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38937643 | |||||||
| chr2:38937694 | A | C | 3 | a0002c0002t0001g0174 a0002c0002t0001g0199 a0002c0002t0001g0200 |
3 | NA18977.hp1 NA19065.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.790+135A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38937694 | |||||||
| chr2:38937913 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(118): Show |
123 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.790+354C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38937913 | |||||||
| chr2:38938028 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.790+469G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938028 | |||||||
| chr2:38938046 | A | G | 52 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0123 others(49): Show |
52 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(49): Show |
intron_variant | MODIFIER | c.790+487A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938046 | |||||||
| chr2:38938070 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG00738.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.790+511A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938070 | |||||||
| chr2:38938206 | G | C | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.790+647G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938206 | |||||||
| chr2:38938216 | A | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(236): Show |
244 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(241): Show |
intron_variant | MODIFIER | c.790+657A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938216 | |||||||
| chr2:38938332 | G | T | 1 | a0001c0001t0004g0211 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.790+773G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938332 | |||||||
| chr2:38938357 | G | A | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.790+798G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938357 | |||||||
| chr2:38938377 | A | G | 9 | a0001c0001t0002g0222 a0001c0001t0003g0209 a0001c0001t0003g0240 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.790+818A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938377 | |||||||
| chr2:38938425 | G | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG00738.hp2 HG01099.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.790+866G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938425 | |||||||
| chr2:38938597 | C | T | 2 | a0001c0003t0002g0271 a0001c0003t0002g0272 |
2 | NA18991.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.790+1038C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938597 | |||||||
| chr2:38938599 | T | C | 1 | a0002c0002t0001g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.790+1040T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938599 | |||||||
| chr2:38938646 | A | G | 1 | a0001c0001t0002g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.790+1087A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938646 | |||||||
| chr2:38938676 | A | T | 1 | a0002c0002t0001g0080 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.790+1117A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938676 | |||||||
| chr2:38938878 | A | T | 1 | a0001c0001t0001g0203 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.790+1319A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38938878 | |||||||
| chr2:38939032 | T | G | 4 | a0001c0001t0002g0269 a0001c0001t0009g0005 a0007c0011t0016g0210 others(1): Show |
5 | HG02280.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.790+1473T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939032 | |||||||
| chr2:38939061 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.790+1502C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939061 | |||||||
| chr2:38939071 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.790+1512C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939071 | |||||||
| chr2:38939118 | G | A | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.790+1559G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939118 | |||||||
| chr2:38939134 | G | T | 2 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.790+1575G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939134 | |||||||
| chr2:38939435 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(218): Show |
226 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(223): Show |
intron_variant | MODIFIER | c.790+1876T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939435 | |||||||
| chr2:38939478 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.790+1919T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939478 | |||||||
| chr2:38939606 | C | G | 2 | a0001c0001t0001g0103 a0001c0001t0010g0213 |
2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.790+2047C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939606 | |||||||
| chr2:38939612 | A | G | 4 | a0001c0001t0002g0269 a0001c0001t0009g0005 a0007c0011t0016g0210 others(1): Show |
5 | HG02280.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.790+2053A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939612 | |||||||
| chr2:38939933 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.790+2374G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38939933 | |||||||
| chr2:38940067 | C | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.790+2508C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38940067 | |||||||
| chr2:38940190 | A | G | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.790+2631A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38940190 | |||||||
| chr2:38940195 | G | A | 4 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0004g0261 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.790+2636G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38940195 | |||||||
| chr2:38940391 | G | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.790+2832G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38940391 | |||||||
| chr2:38940431 | CT | C | 6 | a0001c0001t0001g0115 a0001c0001t0002g0008 a0001c0001t0003g0224 others(3): Show |
6 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.790+2887delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38940431 | ||||||
| chr2:38940687 | C | T | 2 | a0001c0001t0003g0220 a0001c0001t0003g0224 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.790+3128C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38940687 | |||||||
| chr2:38940868 | A | G | 1 | a0002c0002t0004g0206 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.791-3033A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38940868 | |||||||
| chr2:38941015 | C | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG00738.hp2 HG01099.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.791-2886C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941015 | |||||||
| chr2:38941201 | T | C | 5 | a0001c0001t0002g0038 a0001c0001t0007g0033 a0001c0001t0007g0039 others(2): Show |
5 | HG00741.hp2 HG01081.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.791-2700T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941201 | |||||||
| chr2:38941412 | A | G | 4 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0004g0261 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.791-2489A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941412 | |||||||
| chr2:38941552 | C | CT | 7 | a0001c0001t0002g0028 a0001c0001t0003g0241 a0001c0001t0004g0266 others(4): Show |
7 | HG01978.hp1 HG02572.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.791-2336dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38941552 | ||||||
| chr2:38941673 | G | T | 2 | a0001c0001t0002g0018 a0001c0001t0003g0238 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.791-2228G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941673 | |||||||
| chr2:38941846 | G | A | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.791-2055G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941846 | |||||||
| chr2:38941894 | G | A | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.791-2007G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941894 | |||||||
| chr2:38941947 | T | C | 11 | a0001c0001t0002g0004 a0001c0001t0002g0084 a0001c0001t0002g0215 others(8): Show |
12 | HG01496.hp1 HG02109.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-1954T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38941947 | |||||||
| chr2:38942005 | AT | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(8): Show |
12 | HG00738.hp2 HG01099.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.791-1882delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942005 | ||||||
| chr2:38942005 | ATT | A | 6 | a0001c0001t0002g0270 a0001c0001t0004g0208 a0001c0001t0004g0259 others(3): Show |
6 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.791-1883_791-1882d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942005 | ||||||
| chr2:38942005 | ATTT | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(202): Show |
208 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.791-1884_791-1882d others(5): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942005 | ||||||
| chr2:38942131 | C | G | 3 | a0001c0001t0002g0269 a0001c0001t0009g0005 a0011c0008t0004g0214 |
4 | HG02280.hp1 HG02818.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.791-1770C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942131 | |||||||
| chr2:38942140 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.791-1761T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942140 | |||||||
| chr2:38942164 | CT | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0072 others(114): Show |
119 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.791-1717delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942164 | ||||||
| chr2:38942164 | CTT | C | 36 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0002g0024 others(33): Show |
36 | HG01106.hp2 HG01243.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.791-1718_791-1717d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942164 | ||||||
| chr2:38942212 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.791-1689A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942212 | |||||||
| chr2:38942304 | C | T | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.791-1597C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942304 | |||||||
| chr2:38942468 | C | CT | 17 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0124 others(14): Show |
17 | HG01167.hp1 HG01169.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.791-1416dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942468 | ||||||
| chr2:38942468 | C | CTT | 102 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(99): Show |
104 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.791-1417_791-1416d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942468 | ||||||
| chr2:38942468 | C | CTTT | 49 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0090 others(46): Show |
50 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.791-1418_791-1416d others(5): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942468 | ||||||
| chr2:38942468 | CT | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0103 a0001c0001t0001g0114 others(48): Show |
52 | HG00738.hp2 HG01099.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.791-1416delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942468 | ||||||
| chr2:38942468 | CTT | C | 11 | a0001c0001t0002g0269 a0001c0001t0003g0224 a0001c0001t0003g0241 others(8): Show |
12 | HG01361.hp2 HG01993.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-1417_791-1416d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38942468 | ||||||
| chr2:38942692 | C | A | 2 | a0001c0001t0002g0269 a0001c0001t0009g0005 |
3 | HG02280.hp1 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.791-1209C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942692 | |||||||
| chr2:38942711 | G | C | 1 | a0001c0001t0004g0266 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.791-1190G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942711 | |||||||
| chr2:38942900 | T | C | 5 | a0001c0001t0004g0264 a0001c0001t0004g0265 a0001c0003t0004g0204 others(2): Show |
5 | NA18963.hp2 NA18988.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.791-1001T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38942900 | |||||||
| chr2:38943013 | C | T | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.791-888C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943013 | |||||||
| chr2:38943267 | T | C | 3 | a0001c0001t0001g0103 a0001c0003t0002g0271 a0001c0003t0002g0272 |
3 | NA18991.hp2 NA19030.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.791-634T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943267 | |||||||
| chr2:38943542 | TG | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(206): Show |
212 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.791-353delG | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38943542 | ||||||
| chr2:38943612 | T | G | 4 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0004g0261 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.791-289T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943612 | |||||||
| chr2:38943691 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.791-210C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943691 | |||||||
| chr2:38943718 | T | A | 1 | a0001c0001t0001g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.791-183T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943718 | |||||||
| chr2:38943720 | G | A | 33 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0002g0223 others(30): Show |
33 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.791-181G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943720 | |||||||
| chr2:38943720 | G | T | 1 | a0001c0001t0002g0217 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.791-181G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943720 | |||||||
| chr2:38943751 | G | C | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.791-150G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943751 | |||||||
| chr2:38943791 | GT | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(156): Show |
162 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.791-100delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 38943791 | ||||||
| chr2:38943817 | C | A | 11 | a0001c0001t0002g0004 a0001c0001t0002g0084 a0001c0001t0002g0215 others(8): Show |
12 | HG01496.hp1 HG02109.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-84C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | chr2 | 38943817 | |||||||
| chr2:38944123 | G | A | 2 | a0007c0011t0016g0210 a0011c0008t0004g0214 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.920+93G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944123 | |||||||
| chr2:38944155 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920+125A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944155 | |||||||
| chr2:38944216 | T | C | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.920+186T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944216 | |||||||
| chr2:38944291 | C | T | 2 | a0001c0001t0003g0209 a0001c0001t0003g0240 |
2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920+261C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944291 | |||||||
| chr2:38944640 | C | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(213): Show |
220 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(217): Show |
intron_variant | MODIFIER | c.920+610C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944640 | |||||||
| chr2:38944649 | T | A | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.920+619T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944649 | |||||||
| chr2:38944655 | C | G | 9 | a0001c0001t0004g0208 a0001c0001t0004g0264 a0001c0001t0004g0265 others(6): Show |
9 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.920+625C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944655 | |||||||
| chr2:38944876 | G | GGT | 6 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0003g0230 others(3): Show |
6 | HG01109.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.920+870_920+871dup others(2): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38944876 | ||||||
| chr2:38944876 | G | GGTGT | 163 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(160): Show |
167 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.920+868_920+871dup others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38944876 | ||||||
| chr2:38944876 | G | GGTGTGT | 13 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0002g0007 others(10): Show |
13 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.920+866_920+871dup others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38944876 | ||||||
| chr2:38944876 | G | GGTGTGTG others(1): Show |
33 | a0001c0001t0001g0003 a0001c0001t0001g0106 a0001c0001t0001g0114 others(30): Show |
34 | HG00738.hp2 HG01099.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.920+864_920+871dup others(8): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38944876 | ||||||
| chr2:38944876 | G | GGTGTGTG others(3): Show |
10 | a0001c0001t0001g0107 a0001c0001t0002g0223 a0001c0001t0003g0209 others(7): Show |
10 | HG01069.hp1 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+862_920+871dup others(10): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38944876 | ||||||
| chr2:38944902 | C | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(218): Show |
226 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(223): Show |
intron_variant | MODIFIER | c.920+872C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944902 | |||||||
| chr2:38944922 | C | A | 2 | a0001c0001t0005g0014 a0001c0001t0005g0015 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.920+892C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38944922 | |||||||
| chr2:38945323 | A | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
10 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+1293A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945323 | |||||||
| chr2:38945331 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.920+1301G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945331 | |||||||
| chr2:38945336 | G | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(134): Show |
139 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.920+1306G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945336 | |||||||
| chr2:38945402 | A | G | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.920+1372A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945402 | |||||||
| chr2:38945456 | G | A | 1 | a0001c0001t0002g0016 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.920+1426G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945456 | |||||||
| chr2:38945587 | A | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.920+1557A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945587 | |||||||
| chr2:38945706 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.920+1676G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945706 | |||||||
| chr2:38945971 | A | G | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.920+1941A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38945971 | |||||||
| chr2:38946064 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.920+2034A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946064 | |||||||
| chr2:38946165 | A | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.920+2135A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946165 | |||||||
| chr2:38946169 | G | A | 2 | a0001c0001t0002g0222 a0001c0001t0002g0270 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.920+2139G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946169 | |||||||
| chr2:38946253 | A | G | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.920+2223A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946253 | |||||||
| chr2:38946429 | CCTT | C | 23 | a0001c0001t0001g0119 a0001c0001t0002g0025 a0001c0001t0002g0027 others(20): Show |
23 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.920+2403_920+2405d others(5): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38946429 | ||||||
| chr2:38946433 | CT | C | 3 | a0001c0001t0001g0113 a0001c0001t0001g0196 a0001c0001t0007g0046 |
3 | HG00323.hp1 HG01081.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.920+2409delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 38946433 | ||||||
| chr2:38946456 | C | T | 1 | a0001c0001t0005g0013 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.920+2426C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946456 | |||||||
| chr2:38946481 | C | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
10 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+2451C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946481 | |||||||
| chr2:38946756 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.920+2726G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946756 | |||||||
| chr2:38946982 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.920+2952T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38946982 | |||||||
| chr2:38947134 | A | C | 1 | a0001c0001t0003g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.920+3104A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947134 | |||||||
| chr2:38947191 | A | T | 3 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | HG02717.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.920+3161A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947191 | |||||||
| chr2:38947424 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.920+3394G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947424 | |||||||
| chr2:38947553 | T | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
10 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.921-3436T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947553 | |||||||
| chr2:38947735 | G | A | 1 | a0001c0001t0003g0243 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.921-3254G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947735 | |||||||
| chr2:38947819 | T | A | 4 | a0002c0002t0001g0176 a0002c0002t0001g0180 a0002c0002t0001g0185 others(1): Show |
4 | HG02602.hp2 HG03710.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-3170T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947819 | |||||||
| chr2:38947837 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.921-3152G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947837 | |||||||
| chr2:38947841 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.921-3148G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38947841 | |||||||
| chr2:38948126 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.921-2863G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38948126 | |||||||
| chr2:38948359 | T | A | 2 | a0001c0001t0003g0230 a0001c0001t0003g0248 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.921-2630T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38948359 | |||||||
| chr2:38948393 | T | C | 2 | a0001c0001t0002g0222 a0001c0001t0002g0270 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.921-2596T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38948393 | |||||||
| chr2:38948778 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.921-2211A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38948778 | |||||||
| chr2:38948876 | G | A | 26 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0002g0223 others(23): Show |
26 | HG01106.hp2 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.921-2113G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38948876 | |||||||
| chr2:38949474 | C | G | 1 | a0001c0001t0003g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.921-1515C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38949474 | |||||||
| chr2:38949554 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(165): Show |
171 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.921-1435A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38949554 | |||||||
| chr2:38949661 | T | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
10 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.921-1328T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38949661 | |||||||
| chr2:38950179 | C | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(216): Show |
223 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(220): Show |
intron_variant | MODIFIER | c.921-810C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950179 | |||||||
| chr2:38950193 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.921-796G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950193 | |||||||
| chr2:38950387 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | NA18945.hp1 NA18952.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.921-602C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950387 | |||||||
| chr2:38950512 | C | T | 8 | a0001c0001t0004g0264 a0001c0001t0004g0265 a0001c0001t0004g0266 others(5): Show |
8 | HG02572.hp2 HG03225.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.921-477C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950512 | |||||||
| chr2:38950631 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0002g0035 |
2 | HG01433.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.921-358G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950631 | |||||||
| chr2:38950670 | G | A | 2 | a0001c0001t0002g0044 a0001c0001t0002g0047 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.921-319G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950670 | |||||||
| chr2:38950692 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.921-297C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950692 | |||||||
| chr2:38950773 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | NA19070.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.921-216C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950773 | |||||||
| chr2:38950817 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.921-172G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950817 | |||||||
| chr2:38950853 | A | T | 1 | a0001c0001t0004g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.921-136A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950853 | |||||||
| chr2:38950904 | G | C | 1 | a0001c0001t0006g0251 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.921-85G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 10/17 | chr2 | 38950904 | |||||||
| chr2:38951272 | T | C | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1053+151T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951272 | |||||||
| chr2:38951352 | G | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(227): Show |
235 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.1053+231G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951352 | |||||||
| chr2:38951377 | A | T | 13 | a0001c0001t0002g0223 a0001c0001t0003g0220 a0001c0001t0003g0221 others(10): Show |
13 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1053+256A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951377 | |||||||
| chr2:38951610 | A | T | 1 | a0001c0001t0002g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1053+489A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951610 | |||||||
| chr2:38951640 | TATATATA others(25): Show |
T | 1 | a0001c0001t0013g0145 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1053+538_1053+569d others(34): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 38951640 | ||||||
| chr2:38951659 | A | G | 3 | a0001c0001t0003g0230 a0001c0001t0003g0241 a0001c0001t0010g0213 |
3 | HG02886.hp2 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1053+538A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951659 | |||||||
| chr2:38951713 | A | G | 34 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0002g0223 others(31): Show |
34 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1053+592A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951713 | |||||||
| chr2:38951718 | C | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(164): Show |
170 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.1053+597C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951718 | |||||||
| chr2:38951722 | T | G | 1 | a0001c0001t0001g0178 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1053+601T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951722 | |||||||
| chr2:38951743 | C | CAT | 12 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(9): Show |
13 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1053+632_1053+633d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 38951743 | ||||||
| chr2:38951819 | A | T | 2 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1053+698A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951819 | |||||||
| chr2:38951868 | A | G | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | HG01074.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1053+747A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38951868 | |||||||
| chr2:38952120 | A | T | 1 | a0001c0001t0006g0257 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1053+999A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952120 | |||||||
| chr2:38952366 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1054-796T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952366 | |||||||
| chr2:38952399 | A | T | 1 | a0001c0001t0002g0040 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1054-763A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952399 | |||||||
| chr2:38952400 | T | A | 1 | a0001c0001t0002g0040 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1054-762T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952400 | |||||||
| chr2:38952408 | G | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(7): Show |
11 | HG00738.hp2 HG01099.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1054-754G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952408 | |||||||
| chr2:38952617 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1054-545C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952617 | |||||||
| chr2:38952703 | A | AT | 17 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(14): Show |
18 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.1054-446dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 38952703 | ||||||
| chr2:38952887 | C | T | 37 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0270 others(34): Show |
37 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1054-275C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952887 | |||||||
| chr2:38952918 | C | T | 4 | a0001c0001t0004g0259 a0001c0001t0004g0260 a0001c0001t0004g0261 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054-244C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952918 | |||||||
| chr2:38952988 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(164): Show |
170 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.1054-174C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38952988 | |||||||
| chr2:38953082 | T | C | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1054-80T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38953082 | |||||||
| chr2:38953120 | G | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(9): Show |
13 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1054-42G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | chr2 | 38953120 | |||||||
| chr2:38953311 | A | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0168 |
2 | HG01074.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1137+66A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953311 | |||||||
| chr2:38953420 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1137+175C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953420 | |||||||
| chr2:38953553 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1137+308G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953553 | |||||||
| chr2:38953583 | T | A | 1 | a0001c0001t0003g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1137+338T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953583 | |||||||
| chr2:38953655 | T | C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0097 a0001c0001t0001g0114 others(11): Show |
15 | HG00738.hp2 HG01099.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.1137+410T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953655 | |||||||
| chr2:38953671 | C | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
4 | HG01074.hp2 HG01123.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137+426C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953671 | |||||||
| chr2:38953853 | C | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0164 others(11): Show |
15 | HG00738.hp2 HG01099.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1138-520C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953853 | |||||||
| chr2:38953856 | T | C | 19 | a0001c0001t0001g0103 a0001c0001t0001g0172 a0001c0001t0002g0009 others(16): Show |
20 | HG01361.hp2 HG02258.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1138-517T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953856 | |||||||
| chr2:38953942 | G | C | 1 | a0001c0001t0006g0257 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1138-431G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953942 | |||||||
| chr2:38953954 | G | T | 3 | a0002c0002t0001g0174 a0002c0002t0001g0199 a0002c0002t0001g0200 |
3 | NA18977.hp1 NA19065.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1138-419G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38953954 | |||||||
| chr2:38954223 | C | T | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1138-150C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38954223 | |||||||
| chr2:38954231 | T | A | 1 | a0001c0001t0014g0094 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1138-142T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 12/17 | chr2 | 38954231 | |||||||
| chr2:38954558 | T | C | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1221+102T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954558 | |||||||
| chr2:38954633 | CT | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(212): Show |
219 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(216): Show |
intron_variant | MODIFIER | c.1221+195delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38954633 | ||||||
| chr2:38954633 | CTT | C | 5 | a0001c0001t0002g0217 a0001c0001t0003g0231 a0001c0001t0005g0014 others(2): Show |
5 | HG01167.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221+194_1221+195d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38954633 | ||||||
| chr2:38954651 | T | G | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1221+195T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954651 | |||||||
| chr2:38954693 | G | T | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1221+237G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954693 | |||||||
| chr2:38954722 | C | G | 1 | a0001c0001t0002g0021 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1221+266C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954722 | |||||||
| chr2:38954726 | T | C | 3 | a0001c0001t0004g0208 a0001c0003t0004g0204 a0001c0003t0004g0205 |
3 | NA18949.hp1 NA18993.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1221+270T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954726 | |||||||
| chr2:38954789 | A | G | 8 | a0001c0001t0002g0008 a0001c0001t0002g0222 a0001c0001t0002g0270 others(5): Show |
8 | HG01361.hp2 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1221+333A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954789 | |||||||
| chr2:38954806 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1221+350G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954806 | |||||||
| chr2:38954840 | G | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0019 a0001c0001t0002g0269 |
3 | HG02258.hp1 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1221+384G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954840 | |||||||
| chr2:38954880 | C | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(219): Show |
226 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(223): Show |
intron_variant | MODIFIER | c.1221+424C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954880 | |||||||
| chr2:38954921 | G | A | 2 | a0001c0001t0005g0014 a0001c0001t0005g0015 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1221+465G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954921 | |||||||
| chr2:38954921 | G | T | 2 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1221+465G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38954921 | |||||||
| chr2:38955481 | C | CT | 42 | a0001c0001t0001g0157 a0001c0001t0002g0008 a0001c0001t0002g0222 others(39): Show |
42 | HG01106.hp2 HG01243.hp2 HG01361.hp2 others(39): Show |
intron_variant | MODIFIER | c.1221+1050dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38955481 | ||||||
| chr2:38955481 | C | CTT | 22 | a0001c0001t0001g0072 a0001c0001t0001g0097 a0001c0001t0001g0104 others(19): Show |
23 | HG00323.hp2 HG01167.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.1221+1049_1221+105 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38955481 | ||||||
| chr2:38955481 | C | CTTT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(137): Show |
144 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.1221+1048_1221+105 others(7): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38955481 | ||||||
| chr2:38955481 | C | CTTTT | 20 | a0001c0001t0001g0098 a0001c0001t0001g0120 a0001c0001t0001g0121 others(17): Show |
20 | HG01074.hp2 HG01099.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1221+1047_1221+105 others(8): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38955481 | ||||||
| chr2:38955530 | T | C | 1 | a0001c0001t0002g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1221+1074T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955530 | |||||||
| chr2:38955625 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(159): Show |
165 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.1221+1169G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955625 | |||||||
| chr2:38955645 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(230): Show |
238 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(235): Show |
intron_variant | MODIFIER | c.1221+1189A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955645 | |||||||
| chr2:38955716 | G | A | 5 | a0001c0001t0001g0097 a0001c0001t0001g0157 a0001c0001t0002g0084 others(2): Show |
5 | HG02109.hp1 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222-1183G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955716 | |||||||
| chr2:38955749 | T | G | 2 | a0001c0003t0004g0204 a0001c0003t0004g0205 |
2 | NA18993.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1222-1150T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955749 | |||||||
| chr2:38955830 | C | T | 1 | a0001c0001t0003g0249 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1222-1069C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955830 | |||||||
| chr2:38955942 | G | T | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1222-957G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38955942 | |||||||
| chr2:38956131 | AAC | A | 4 | a0001c0001t0002g0025 a0001c0001t0002g0031 a0001c0001t0002g0048 others(1): Show |
4 | HG00735.hp1 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222-763_1222-762d others(4): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 38956131 | ||||||
| chr2:38956141 | G | A | 2 | a0001c0003t0004g0204 a0001c0003t0004g0205 |
2 | NA18993.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1222-758G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38956141 | |||||||
| chr2:38956272 | A | G | 1 | a0002c0002t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1222-627A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38956272 | |||||||
| chr2:38956488 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1222-411C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38956488 | |||||||
| chr2:38956877 | C | T | 1 | a0002c0002t0001g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1222-22C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38956877 | |||||||
| chr2:38956886 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1222-13C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | chr2 | 38956886 | |||||||
| chr2:38957147 | G | A | 1 | a0002c0002t0001g0181 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1370+100G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957147 | |||||||
| chr2:38957215 | C | T | 7 | a0001c0003t0004g0204 a0001c0003t0004g0205 a0001c0003t0015g0173 others(4): Show |
7 | HG02615.hp2 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1370+168C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957215 | |||||||
| chr2:38957225 | A | G | 6 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0116 others(3): Show |
6 | HG00597.hp1 HG03834.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1370+178A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957225 | |||||||
| chr2:38957368 | T | C | 1 | a0008c0007t0001g0170 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1370+321T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957368 | |||||||
| chr2:38957406 | C | G | 11 | a0001c0001t0006g0239 a0001c0001t0006g0250 a0001c0001t0006g0251 others(8): Show |
11 | HG01106.hp2 HG01993.hp2 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1370+359C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957406 | |||||||
| chr2:38957443 | T | C | 2 | a0001c0001t0009g0005 a0011c0008t0004g0214 |
3 | HG02280.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1370+396T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957443 | |||||||
| chr2:38957451 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1370+404G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957451 | |||||||
| chr2:38957610 | A | C | 9 | a0001c0001t0001g0103 a0001c0001t0002g0008 a0001c0001t0002g0222 others(6): Show |
9 | HG01361.hp2 HG02572.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1371-424A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957610 | |||||||
| chr2:38957773 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1371-261A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957773 | |||||||
| chr2:38957808 | C | G | 1 | a0001c0001t0002g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1371-226C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957808 | |||||||
| chr2:38957823 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0072 a0001c0001t0001g0074 others(90): Show |
95 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1371-211A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957823 | |||||||
| chr2:38957838 | A | G | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1371-196A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957838 | |||||||
| chr2:38957907 | C | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(221): Show |
228 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.1371-127C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957907 | |||||||
| chr2:38957973 | T | C | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1371-61T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957973 | |||||||
| chr2:38957987 | C | T | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1371-47C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 14/17 | chr2 | 38957987 | |||||||
| chr2:38958215 | G | T | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1535+17G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38958215 | |||||||
| chr2:38958248 | A | G | 33 | a0001c0001t0002g0223 a0001c0001t0002g0234 a0001c0001t0003g0209 others(30): Show |
33 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1535+50A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38958248 | |||||||
| chr2:38958672 | G | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(161): Show |
167 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.1535+474G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38958672 | |||||||
| chr2:38958714 | AT | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(221): Show |
228 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.1535+525delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 38958714 | ||||||
| chr2:38958905 | C | T | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1535+707C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38958905 | |||||||
| chr2:38958910 | A | C | 3 | a0001c0001t0004g0208 a0001c0003t0004g0204 a0001c0003t0004g0205 |
3 | NA18949.hp1 NA18993.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1535+712A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38958910 | |||||||
| chr2:38959198 | C | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(221): Show |
228 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.1536-643C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38959198 | |||||||
| chr2:38959392 | C | T | 2 | a0001c0001t0003g0209 a0001c0001t0003g0240 |
2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1536-449C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38959392 | |||||||
| chr2:38959435 | T | G | 4 | a0001c0003t0015g0173 a0001c0004t0004g0075 a0001c0004t0004g0076 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536-406T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38959435 | |||||||
| chr2:38959550 | A | G | 1 | a0006c0010t0005g0063 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1536-291A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38959550 | |||||||
| chr2:38959755 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG01069.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1536-86G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 15/17 | chr2 | 38959755 | |||||||
| chr2:38960884 | G | A | 1 | a0001c0001t0003g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2343+236G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38960884 | |||||||
| chr2:38960887 | C | G | 1 | a0005c0012t0002g0034 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2343+239C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38960887 | |||||||
| chr2:38961036 | C | G | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2343+388C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961036 | |||||||
| chr2:38961158 | G | T | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2343+510G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961158 | |||||||
| chr2:38961369 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(224): Show |
232 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(229): Show |
intron_variant | MODIFIER | c.2343+721A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961369 | |||||||
| chr2:38961540 | G | A | 2 | a0001c0003t0004g0204 a0001c0003t0004g0205 |
2 | NA18993.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2343+892G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961540 | |||||||
| chr2:38961543 | C | T | 1 | a0002c0002t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2343+895C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961543 | |||||||
| chr2:38961551 | C | T | 10 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0153 others(7): Show |
10 | NA18948.hp2 NA18949.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.2343+903C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961551 | |||||||
| chr2:38961579 | A | C | 3 | a0002c0002t0001g0085 a0002c0002t0001g0086 a0002c0002t0001g0087 |
3 | NA18945.hp2 NA18980.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2343+931A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961579 | |||||||
| chr2:38961581 | A | T | 4 | a0001c0003t0015g0173 a0001c0004t0004g0075 a0001c0004t0004g0076 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2343+933A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961581 | |||||||
| chr2:38961774 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(224): Show |
232 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(229): Show |
intron_variant | MODIFIER | c.2343+1126A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961774 | |||||||
| chr2:38961836 | C | T | 1 | a0001c0001t0010g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2343+1188C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961836 | |||||||
| chr2:38961997 | C | G | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2343+1349C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38961997 | |||||||
| chr2:38962176 | T | G | 1 | a0011c0008t0004g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2343+1528T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962176 | |||||||
| chr2:38962421 | G | C | 1 | a0001c0001t0002g0233 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2343+1773G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962421 | |||||||
| chr2:38962495 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(227): Show |
235 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.2343+1847G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962495 | |||||||
| chr2:38962637 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2343+1989A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962637 | |||||||
| chr2:38962657 | C | T | 7 | a0002c0002t0001g0096 a0002c0002t0001g0182 a0002c0002t0001g0187 others(4): Show |
7 | NA18942.hp1 NA18953.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.2343+2009C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962657 | |||||||
| chr2:38962690 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(224): Show |
232 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(229): Show |
intron_variant | MODIFIER | c.2343+2042A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962690 | |||||||
| chr2:38962757 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2343+2109G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962757 | |||||||
| chr2:38962825 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(231): Show |
239 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(236): Show |
intron_variant | MODIFIER | c.2343+2177C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962825 | |||||||
| chr2:38962849 | C | CA | 46 | a0001c0001t0001g0123 a0001c0001t0002g0018 a0001c0001t0002g0222 others(43): Show |
47 | HG01071.hp1 HG01243.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.2343+2226dupA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 38962849 | ||||||
| chr2:38962849 | C | CAA | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(147): Show |
154 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.2343+2225_2343+222 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 38962849 | ||||||
| chr2:38962849 | C | CAAA | 33 | a0001c0001t0001g0073 a0001c0001t0001g0093 a0001c0001t0001g0099 others(30): Show |
33 | HG00597.hp1 HG00735.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.2343+2224_2343+222 others(7): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 38962849 | ||||||
| chr2:38962934 | G | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(221): Show |
228 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(225): Show |
intron_variant | MODIFIER | c.2343+2286G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38962934 | |||||||
| chr2:38963023 | CA | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(210): Show |
217 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.2343+2392delA | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 38963023 | ||||||
| chr2:38963288 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2343+2640T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963288 | |||||||
| chr2:38963355 | T | C | 1 | a0001c0001t0003g0243 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2344-2651T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963355 | |||||||
| chr2:38963569 | A | G | 9 | a0001c0001t0002g0234 a0001c0001t0003g0209 a0001c0001t0003g0240 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2344-2437A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963569 | |||||||
| chr2:38963712 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0002g0069 a0001c0001t0002g0070 |
3 | NA18948.hp2 NA18964.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.2344-2294A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963712 | |||||||
| chr2:38963823 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(206): Show |
213 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(210): Show |
intron_variant | MODIFIER | c.2344-2183C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963823 | |||||||
| chr2:38963844 | C | T | 25 | a0001c0001t0003g0220 a0001c0001t0003g0221 a0001c0001t0003g0224 others(22): Show |
25 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.2344-2162C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963844 | |||||||
| chr2:38963846 | G | A | 8 | a0001c0001t0003g0209 a0001c0001t0003g0240 a0001c0001t0003g0242 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2344-2160G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38963846 | |||||||
| chr2:38964059 | G | A | 4 | a0001c0001t0001g0107 a0001c0001t0004g0266 a0001c0001t0004g0267 others(1): Show |
4 | HG01069.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2344-1947G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38964059 | |||||||
| chr2:38964144 | T | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0114 a0001c0001t0001g0115 others(12): Show |
16 | HG00738.hp2 HG01099.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2344-1862T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38964144 | |||||||
| chr2:38964697 | G | A | 3 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0037 |
3 | HG01074.hp1 HG01256.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2344-1309G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38964697 | |||||||
| chr2:38964837 | T | C | 3 | a0001c0001t0004g0266 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG02572.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2344-1169T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38964837 | |||||||
| chr2:38964849 | T | A | 2 | a0001c0003t0004g0204 a0001c0003t0004g0205 |
2 | NA18993.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2344-1157T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38964849 | |||||||
| chr2:38965097 | A | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2344-909A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38965097 | |||||||
| chr2:38965241 | T | G | 1 | a0002c0002t0001g0192 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2344-765T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38965241 | |||||||
| chr2:38965590 | G | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2344-416G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38965590 | |||||||
| chr2:38965681 | A | T | 13 | a0001c0001t0001g0119 a0001c0001t0002g0025 a0001c0001t0002g0030 others(10): Show |
13 | HG00735.hp1 HG00741.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2344-325A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38965681 | |||||||
| chr2:38965836 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2344-170C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38965836 | |||||||
| chr2:38965964 | T | A | 5 | a0001c0001t0002g0008 a0001c0001t0002g0222 a0001c0001t0002g0270 others(2): Show |
5 | HG01361.hp2 HG02895.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2344-42T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | chr2 | 38965964 | |||||||
| chr2:38966189 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2483+44T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966189 | |||||||
| chr2:38966195 | T | A | 8 | a0001c0001t0002g0008 a0001c0001t0002g0222 a0001c0001t0002g0270 others(5): Show |
8 | HG01361.hp2 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.2483+50T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966195 | |||||||
| chr2:38966289 | G | A | 5 | a0001c0001t0001g0117 a0001c0001t0001g0167 a0001c0001t0005g0012 others(2): Show |
5 | HG01192.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2483+144G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966289 | |||||||
| chr2:38966311 | T | C | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2483+166T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966311 | |||||||
| chr2:38966384 | T | C | 1 | a0001c0001t0002g0223 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2483+239T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966384 | |||||||
| chr2:38966540 | G | A | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2483+395G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966540 | |||||||
| chr2:38966596 | C | A | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2483+451C>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966596 | |||||||
| chr2:38966606 | T | A | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2483+461T>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966606 | |||||||
| chr2:38966613 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2483+468G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966613 | |||||||
| chr2:38966690 | T | C | 1 | a0001c0001t0003g0249 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2483+545T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966690 | |||||||
| chr2:38966772 | C | G | 1 | a0001c0001t0003g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2483+627C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966772 | |||||||
| chr2:38966813 | A | G | 1 | a0006c0010t0005g0063 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2483+668A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38966813 | |||||||
| chr2:38967215 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2483+1070G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967215 | |||||||
| chr2:38967243 | G | A | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2483+1098G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967243 | |||||||
| chr2:38967444 | G | A | 2 | a0001c0001t0002g0027 a0001c0001t0002g0060 |
2 | NA19001.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2483+1299G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967444 | |||||||
| chr2:38967453 | A | C | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2483+1308A>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967453 | |||||||
| chr2:38967606 | G | C | 1 | a0001c0001t0009g0005 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2483+1461G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967606 | |||||||
| chr2:38967637 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2483+1492G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967637 | |||||||
| chr2:38967742 | A | AT | 10 | a0001c0001t0001g0091 a0001c0001t0001g0134 a0001c0001t0002g0016 others(7): Show |
10 | HG00597.hp2 HG02055.hp1 HG04199.hp1 others(7): Show |
intron_variant | MODIFIER | c.2483+1615dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 38967742 | ||||||
| chr2:38967772 | A | G | 1 | a0001c0001t0002g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2483+1627A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967772 | |||||||
| chr2:38967906 | C | T | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2483+1761C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967906 | |||||||
| chr2:38967936 | C | CT | 8 | a0001c0001t0001g0141 a0001c0001t0001g0159 a0001c0001t0004g0262 others(5): Show |
8 | HG02818.hp2 HG03710.hp2 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.2483+1819dupT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 38967936 | ||||||
| chr2:38967936 | CT | C | 54 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0103 others(51): Show |
55 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.2483+1819delT | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 38967936 | ||||||
| chr2:38967936 | CTT | C | 5 | a0001c0001t0003g0229 a0001c0001t0003g0240 a0001c0004t0004g0075 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2483+1818_2483+181 others(6): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 38967936 | ||||||
| chr2:38967936 | CTTTTTTT others(4): Show |
C | 17 | a0001c0001t0001g0099 a0001c0001t0002g0006 a0001c0001t0002g0007 others(14): Show |
17 | HG01106.hp1 HG01109.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.2483+1809_2483+181 others(15): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 38967936 | ||||||
| chr2:38967986 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2483+1841A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38967986 | |||||||
| chr2:38968172 | A | T | 4 | a0001c0001t0001g0161 a0001c0001t0002g0069 a0001c0001t0002g0070 others(1): Show |
4 | NA18948.hp2 NA18964.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.2483+2027A>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38968172 | |||||||
| chr2:38968225 | C | G | 1 | a0001c0001t0009g0005 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2483+2080C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38968225 | |||||||
| chr2:38968490 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2483+2345T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38968490 | |||||||
| chr2:38968587 | G | T | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2483+2442G>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38968587 | |||||||
| chr2:38968688 | A | G | 1 | a0007c0011t0016g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2483+2543A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38968688 | |||||||
| chr2:38968874 | G | A | 1 | a0001c0001t0003g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2483+2729G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38968874 | |||||||
| chr2:38969255 | C | G | 1 | a0001c0001t0013g0145 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2483+3110C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38969255 | |||||||
| chr2:38969315 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2483+3170T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38969315 | |||||||
| chr2:38969585 | T | C | 3 | a0001c0001t0002g0008 a0001c0001t0002g0222 a0001c0001t0002g0270 |
3 | HG02895.hp2 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2483+3440T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38969585 | |||||||
| chr2:38969783 | A | G | 7 | a0001c0001t0002g0027 a0001c0001t0002g0055 a0001c0001t0002g0057 others(4): Show |
7 | NA18960.hp2 NA18988.hp1 NA18997.hp2 others(4): Show |
intron_variant | MODIFIER | c.2483+3638A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38969783 | |||||||
| chr2:38969836 | C | T | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2483+3691C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38969836 | |||||||
| chr2:38969881 | A | G | 1 | a0001c0003t0015g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2483+3736A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38969881 | |||||||
| chr2:38970181 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2484-3533A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38970181 | |||||||
| chr2:38970402 | G | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(230): Show |
238 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(235): Show |
intron_variant | MODIFIER | c.2484-3312G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38970402 | |||||||
| chr2:38970513 | A | G | 2 | a0001c0001t0006g0250 a0001c0001t0006g0251 |
2 | HG01106.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.2484-3201A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38970513 | |||||||
| chr2:38970605 | A | G | 1 | a0002c0002t0001g0192 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2484-3109A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38970605 | |||||||
| chr2:38970895 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(190): Show |
198 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.2484-2819A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38970895 | |||||||
| chr2:38971825 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(223): Show |
231 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(228): Show |
intron_variant | MODIFIER | c.2484-1889A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38971825 | |||||||
| chr2:38972074 | G | A | 1 | a0001c0001t0005g0013 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2484-1640G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972074 | |||||||
| chr2:38972130 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(229): Show |
237 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(234): Show |
intron_variant | MODIFIER | c.2484-1584T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972130 | |||||||
| chr2:38972268 | G | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0135 a0001c0001t0001g0139 |
3 | HG00609.hp2 HG01943.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2484-1446G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972268 | |||||||
| chr2:38972302 | G | C | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2484-1412G>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972302 | |||||||
| chr2:38972395 | T | C | 1 | a0001c0001t0009g0005 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2484-1319T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972395 | |||||||
| chr2:38972511 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2484-1203G>A | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972511 | |||||||
| chr2:38972542 | A | G | 14 | a0001c0001t0002g0223 a0001c0001t0003g0220 a0001c0001t0003g0221 others(11): Show |
14 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2484-1172A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972542 | |||||||
| chr2:38972561 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(231): Show |
239 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(236): Show |
intron_variant | MODIFIER | c.2484-1153C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972561 | |||||||
| chr2:38972615 | A | G | 1 | a0001c0001t0003g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2484-1099A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972615 | |||||||
| chr2:38972739 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(224): Show |
232 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(229): Show |
intron_variant | MODIFIER | c.2484-975A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972739 | |||||||
| chr2:38972804 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2484-910A>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972804 | |||||||
| chr2:38972814 | C | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0072 others(163): Show |
169 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.2484-900C>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972814 | |||||||
| chr2:38972908 | T | C | 3 | a0001c0004t0004g0075 a0001c0004t0004g0076 a0001c0004t0011g0077 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2484-806T>C | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38972908 | |||||||
| chr2:38973057 | T | G | 10 | a0001c0001t0001g0083 a0001c0001t0001g0117 a0001c0001t0001g0167 others(7): Show |
10 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2484-657T>G | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38973057 | |||||||
| chr2:38973220 | AC | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0017 others(3): Show |
6 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2484-492delC | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 38973220 | ||||||
| chr2:38973531 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2484-183C>T | ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 17/17 | chr2 | 38973531 |