Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10810 |
| ensemblid | ENSG00000132970.14 |
| hgncid | 12734 |
| symbol | WASF3 |
| name | WASP family member 3 |
| refseq_nuc | NM_006646.6 |
| refseq_prot | NP_006637.2 |
| ensembl_nuc | ENST00000335327.6 |
| ensembl_prot | ENSP00000335055.5 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 26557683 |
| end | 26688948 |
| strand | + |
| ver | v1.2 |
| region | chr13:26557683-26688948 |
| region5000 | chr13:26552683-26693948 |
| regionname0 | WASF3_chr13_26557683_26688948 |
| regionname5000 | WASF3_chr13_26552683_26693948 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 502 | 270 | 69 | 58 | 104 | 10 | 27 | 71 | WASF3_chr13_26552683_26693948 | WASF3 | MPLVK others(497): Show |
chr13 | 26552683 | 26693948 |
| a0002 | 0/0 | 502 | 20 | 8 | 4 | 7 | 0 | 1 | 2 | WASF3_chr13_26552683_26693948 | WASF3 | MPLVK others(497): Show |
chr13 | 26552683 | 26693948 |
| a0003 | 0/0 | 502 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | MPLVK others(497): Show |
chr13 | 26552683 | 26693948 |
| a0004 | 0/0 | 502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | MPLVK others(497): Show |
chr13 | 26552683 | 26693948 |
| a0005 | 0/0 | 502 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | MPLVK others(497): Show |
chr13 | 26552683 | 26693948 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1506 | 210 | 35 | 45 | 100 | 6 | 22 | WASF3_chr13_26552683_26693948 | WASF3 | ATGCC others(1501): Show |
chr13 | 26552683 | 26693948 | ||
| a0001c0002 | 0/0 | 1506 | 55 | 30 | 13 | 3 | 4 | 5 | WASF3_chr13_26552683_26693948 | WASF3 | ATGCC others(1501): Show |
chr13 | 26552683 | 26693948 | ||
| a0001c0004 | 0/0 | 1506 | 4 | 4 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | ATGCC others(1501): Show |
chr13 | 26552683 | 26693948 | ||
| a0001c0007 | 0/0 | 1506 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | ATGCC others(1501): Show |
chr13 | 26552683 | 26693948 | ||
| a0002c0003 | 0/0 | 1506 | 20 | 8 | 4 | 7 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | ATGCC others(1501): Show |
chr13 | 26552683 | 26693948 | ||
| a0003c0005 | 0/0 | 1506 | 2 | 2 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | ATGCC others(1501): Show |
chr13 | 26552683 | 26693948 | ||
| a0004c0008 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | ATGCC others(1501): Show |
chr13 | 26552683 | 26693948 | ||
| a0005c0006 | 0/0 | 1506 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | ATGCC others(1501): Show |
chr13 | 26552683 | 26693948 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4860 | 87 | 11 | 17 | 49 | 2 | 8 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4855): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0002 | 0/1 | 4858 | 69 | 8 | 9 | 38 | 4 | 9 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4853): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0005 | 0/0 | 4858 | 16 | 0 | 11 | 2 | 0 | 3 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4853): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0007 | 0/0 | 4859 | 8 | 8 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4854): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0008 | 1/0 | 4857 | 5 | 4 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4852): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0010 | 0/0 | 4859 | 6 | 1 | 0 | 3 | 0 | 2 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4854): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0012 | 0/0 | 4860 | 4 | 0 | 4 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4855): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0014 | 0/0 | 4842 | 2 | 0 | 0 | 2 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4837): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0015 | 0/0 | 4861 | 2 | 1 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4856): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0020 | 0/0 | 4857 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4852): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0021 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4855): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0022 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4855): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0023 | 0/0 | 4859 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4854): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0029 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4855): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0032 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4855): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0033 | 0/0 | 4856 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4851): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0034 | 0/0 | 4857 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4852): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0037 | 0/0 | 4860 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4855): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0038 | 0/0 | 4858 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4853): Show |
chr13 | 26552683 | 26693948 |
| a0001c0001t0039 | 0/0 | 4857 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4852): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0003 | 0/0 | 4834 | 3 | 1 | 1 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4829): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0004 | 0/0 | 4836 | 17 | 2 | 7 | 3 | 3 | 2 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4831): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0006 | 0/0 | 4834 | 13 | 10 | 2 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4829): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0009 | 0/0 | 4860 | 7 | 7 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4855): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0011 | 0/0 | 4834 | 2 | 2 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4829): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0016 | 0/0 | 4834 | 2 | 1 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4829): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0017 | 0/0 | 4834 | 2 | 0 | 1 | 0 | 1 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4829): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0018 | 0/0 | 4835 | 2 | 1 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4830): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0019 | 0/0 | 4834 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4829): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0025 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4856): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0026 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4852): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0028 | 0/0 | 4835 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4830): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0030 | 0/0 | 4835 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4830): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0031 | 0/0 | 4859 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4854): Show |
chr13 | 26552683 | 26693948 |
| a0001c0002t0035 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4852): Show |
chr13 | 26552683 | 26693948 |
| a0001c0004t0013 | 0/0 | 4857 | 3 | 3 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4852): Show |
chr13 | 26552683 | 26693948 |
| a0001c0004t0024 | 0/0 | 4853 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4848): Show |
chr13 | 26552683 | 26693948 |
| a0001c0007t0002 | 0/0 | 4858 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4853): Show |
chr13 | 26552683 | 26693948 |
| a0002c0003t0003 | 0/0 | 4834 | 16 | 4 | 4 | 7 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4829): Show |
chr13 | 26552683 | 26693948 |
| a0002c0003t0011 | 0/0 | 4834 | 3 | 3 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4829): Show |
chr13 | 26552683 | 26693948 |
| a0002c0003t0027 | 0/0 | 4835 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4830): Show |
chr13 | 26552683 | 26693948 |
| a0003c0005t0008 | 0/0 | 4857 | 2 | 2 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4852): Show |
chr13 | 26552683 | 26693948 |
| a0004c0008t0036 | 0/0 | 4857 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4852): Show |
chr13 | 26552683 | 26693948 |
| a0005c0006t0002 | 0/0 | 4858 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | GTGGA others(4853): Show |
chr13 | 26552683 | 26693948 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0002 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0025 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0008g0247 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0008g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0010g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0010g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0010g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0010g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0012g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0012g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0012g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0012g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0014g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0014g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0015g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0020g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0021g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0022g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0023g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0029g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0032g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0033g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0034g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0037g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0038g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0001t0039g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0006g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0006g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0006g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0009g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0009g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0011g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0016g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0016g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0017g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0017g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0018g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0019g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0025g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0026g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0028g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0030g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0031g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0002t0035g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0004t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0004t0013g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0004t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0004t0024g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0001c0007t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0011g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0002c0003t0027g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0003c0005t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0003c0005t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0004c0008t0036g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| a0005c0006t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0004 | g0236 | EUR | GBR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0041 | EUR | GBR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00280 | hp1 | a0001 | c0002 | t0004 | g0235 | EUR | FIN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | FIN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | CHS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00423 | hp1 | a0002 | c0003 | t0003 | g0051 | EAS | CHS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | CHS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0265 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00735 | hp1 | a0002 | c0003 | t0003 | g0063 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0256 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00738 | hp2 | a0001 | c0002 | t0016 | g0014 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01069 | hp1 | a0002 | c0003 | t0003 | g0080 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01069 | hp2 | a0001 | c0002 | t0004 | g0226 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0037 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01074 | hp2 | a0001 | c0002 | t0004 | g0228 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01081 | hp1 | a0001 | c0002 | t0017 | g0232 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0269 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01099 | hp1 | a0001 | c0002 | t0004 | g0231 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01109 | hp2 | a0001 | c0001 | t0015 | g0015 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01168 | hp1 | a0001 | c0001 | t0012 | g0194 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0268 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01175 | hp1 | a0001 | c0002 | t0018 | g0023 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01192 | hp1 | a0001 | c0002 | t0006 | g0107 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0022 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01243 | hp2 | a0001 | c0001 | t0020 | g0026 | AMR | PUR | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0262 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0261 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01358 | hp1 | a0001 | c0001 | t0037 | g0292 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01358 | hp2 | a0001 | c0001 | t0038 | g0258 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0234 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0270 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01496 | hp2 | a0001 | c0001 | t0012 | g0193 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01515 | hp1 | a0001 | c0002 | t0017 | g0229 | EUR | IBS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0281 | EUR | IBS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | IBS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0273 | EUR | IBS | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01891 | hp2 | a0002 | c0003 | t0003 | g0099 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0271 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01934 | hp2 | a0001 | c0001 | t0012 | g0192 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0263 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0260 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01981 | hp2 | a0001 | c0002 | t0004 | g0225 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02027 | hp2 | a0001 | c0001 | t0014 | g0118 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02055 | hp1 | a0001 | c0002 | t0026 | g0204 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02055 | hp2 | a0001 | c0001 | t0021 | g0004 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02071 | hp1 | a0002 | c0003 | t0003 | g0062 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02074 | hp1 | a0001 | c0001 | t0023 | g0094 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02080 | hp1 | a0002 | c0003 | t0003 | g0052 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02145 | hp1 | a0001 | c0002 | t0025 | g0206 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02145 | hp2 | a0001 | c0001 | t0015 | g0017 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02148 | hp1 | a0001 | c0002 | t0006 | g0031 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02148 | hp2 | a0002 | c0003 | t0003 | g0070 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CDX | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CDX | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02165 | hp1 | a0002 | c0003 | t0003 | g0056 | EAS | CDX | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CDX | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0249 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02257 | hp2 | a0002 | c0003 | t0003 | g0066 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02258 | hp1 | a0001 | c0002 | t0006 | g0243 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02258 | hp2 | a0003 | c0005 | t0008 | g0252 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0259 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02273 | hp2 | a0001 | c0001 | t0012 | g0191 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02280 | hp1 | a0001 | c0002 | t0006 | g0242 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02280 | hp2 | a0002 | c0003 | t0027 | g0104 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02293 | hp1 | a0002 | c0003 | t0003 | g0089 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02451 | hp2 | a0001 | c0002 | t0006 | g0106 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02523 | hp1 | a0002 | c0003 | t0003 | g0049 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02602 | hp1 | a0001 | c0001 | t0010 | g0220 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0266 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02622 | hp1 | a0001 | c0002 | t0011 | g0215 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02683 | hp2 | a0001 | c0001 | t0010 | g0221 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0267 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02717 | hp1 | a0001 | c0002 | t0006 | g0246 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02717 | hp2 | a0001 | c0004 | t0013 | g0033 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02723 | hp1 | a0001 | c0004 | t0013 | g0197 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02723 | hp2 | a0001 | c0002 | t0006 | g0035 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0152 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02735 | hp2 | a0001 | c0002 | t0004 | g0223 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02809 | hp1 | a0001 | c0002 | t0006 | g0034 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0087 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02818 | hp1 | a0001 | c0002 | t0003 | g0038 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0086 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02886 | hp1 | a0002 | c0003 | t0011 | g0013 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02886 | hp2 | a0001 | c0001 | t0022 | g0168 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02922 | hp1 | a0004 | c0008 | t0036 | g0018 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02965 | hp1 | a0001 | c0004 | t0024 | g0196 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02965 | hp2 | a0001 | c0002 | t0016 | g0010 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02976 | hp1 | a0002 | c0003 | t0003 | g0098 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0105 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0021 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03041 | hp2 | a0001 | c0002 | t0009 | g0003 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0250 | AFR | MSL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03098 | hp2 | a0001 | c0002 | t0031 | g0214 | AFR | MSL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0110 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0245 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03139 | hp1 | a0002 | c0003 | t0003 | g0201 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03195 | hp1 | a0001 | c0002 | t0009 | g0209 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0085 | AFR | MSL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03225 | hp2 | a0001 | c0002 | t0009 | g0212 | AFR | MSL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03453 | hp1 | a0001 | c0002 | t0035 | g0210 | AFR | MSL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03486 | hp1 | a0003 | c0005 | t0008 | g0251 | AFR | MSL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03516 | hp1 | a0001 | c0002 | t0006 | g0244 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | ESN | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0248 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | GWD | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03579 | hp1 | a0001 | c0002 | t0009 | g0205 | AFR | MSL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03579 | hp2 | a0001 | c0002 | t0011 | g0216 | AFR | MSL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | BEB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03834 | hp2 | a0001 | c0002 | t0030 | g0227 | SAS | BEB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0264 | SAS | BEB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03927 | hp2 | a0002 | c0003 | t0003 | g0050 | SAS | BEB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03942 | hp1 | a0001 | c0002 | t0004 | g0224 | SAS | BEB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | BEB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | STU | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | STU | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG04204 | hp2 | a0001 | c0002 | t0006 | g0030 | SAS | STU | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18522 | hp1 | a0002 | c0003 | t0011 | g0012 | AFR | YRI | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18522 | hp2 | a0001 | c0002 | t0009 | g0208 | AFR | YRI | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | CHB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | YRI | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0045 | AFR | YRI | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18939 | hp2 | a0001 | c0001 | t0039 | g0257 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18946 | hp1 | a0001 | c0001 | t0014 | g0143 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18951 | hp2 | a0002 | c0003 | t0003 | g0081 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18954 | hp1 | a0001 | c0002 | t0004 | g0238 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18961 | hp2 | a0001 | c0001 | t0010 | g0162 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0255 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18982 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18982 | hp2 | a0001 | c0007 | t0002 | g0040 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18991 | hp1 | a0002 | c0003 | t0003 | g0048 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18999 | hp1 | a0001 | c0002 | t0004 | g0240 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA18999 | hp2 | a0001 | c0001 | t0029 | g0157 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19001 | hp2 | a0001 | c0001 | t0034 | g0203 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19007 | hp2 | a0001 | c0002 | t0004 | g0241 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19030 | hp1 | a0001 | c0004 | t0013 | g0195 | AFR | LWK | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0044 | AFR | LWK | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19043 | hp1 | a0001 | c0002 | t0028 | g0222 | AFR | LWK | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19043 | hp2 | a0001 | c0002 | t0006 | g0213 | AFR | LWK | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19057 | hp1 | a0005 | c0006 | t0002 | g0057 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19058 | hp2 | a0001 | c0001 | t0010 | g0182 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19064 | hp1 | a0001 | c0001 | t0032 | g0101 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19090 | hp1 | a0001 | c0001 | t0033 | g0100 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA20129 | hp2 | a0001 | c0002 | t0009 | g0211 | AFR | ASW | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0068 | EUR | TSI | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA20805 | hp2 | a0001 | c0002 | t0004 | g0233 | EUR | TSI | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | GIH | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | GIH | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG01123 | hp2 | a0001 | c0002 | t0004 | g0237 | AMR | CLM | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02109 | hp1 | a0001 | c0002 | t0018 | g0020 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02109 | hp2 | a0002 | c0003 | t0011 | g0011 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG02486 | hp2 | a0001 | c0002 | t0006 | g0032 | AFR | ACB | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG03471 | hp2 | a0001 | c0002 | t0009 | g0207 | AFR | MSL | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG06807 | hp1 | a0001 | c0002 | t0004 | g0230 | AFR | USA | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0027 | AFR | USA | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA20300 | hp1 | a0001 | c0002 | t0019 | g0217 | AFR | USA | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | USA | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0088 | AFR | LWK | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0025 | REF | REF | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0247 | REF | REF | WASF3_chr13_26552683_26693948 | WASF3 | chr13 | 26552683 | 26693948 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:26681070 | G | A | 1 | a0005 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.733G>A | p.Val245Ile | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/10 | 978/4857 | 733/1509 | 245/502 | chr13 | 26681070 | |||
| chr13:26682867 | C | T | 1 | a0002 | 20 | HG00423.hp1 HG00735.hp1 HG01069.hp1 others(17): Show |
missense_variant | MODERATE | c.1244C>T | p.Ser415Leu | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/10 | 1489/4857 | 1244/1509 | 415/502 | chr13 | 26682867 | |||
| chr13:26682932 | A | G | 1 | a0003 | 2 | HG02258.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.1309A>G | p.Ile437Val | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/10 | 1554/4857 | 1309/1509 | 437/502 | chr13 | 26682932 | |||
| chr13:26685840 | G | A | 1 | a0004 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1504G>A | p.Asp502Asn | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1749/4857 | 1504/1509 | 502/502 | chr13 | 26685840 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:26676686 | T | C | 2 | a0001c0002 a0002c0003 |
75 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(72): Show |
synonymous_variant | LOW | c.678T>C | p.His226His | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/10 | 923/4857 | 678/1509 | 226/502 | chr13 | 26676686 | |||
| chr13:26681300 | G | A | 1 | a0001c0004 | 4 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.963G>A | p.Pro321Pro | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/10 | 1208/4857 | 963/1509 | 321/502 | chr13 | 26681300 | |||
| chr13:26685725 | G | A | 1 | a0001c0007 | 1 | NA18982.hp2 | synonymous_variant | LOW | c.1389G>A | p.Gln463Gln | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1634/4857 | 1389/1509 | 463/502 | chr13 | 26685725 | |||
| chr13:26685839 | C | T | 1 | a0003c0005 | 2 | HG02258.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.1503C>T | p.Ser501Ser | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1748/4857 | 1503/1509 | 501/502 | chr13 | 26685839 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:26557689 | G | T | 4 | a0001c0001t0005 a0001c0001t0037 a0001c0001t0038 others(1): Show |
19 | HG00639.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-239G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/10 | chr13 | 26557689 | |||||||
| chr13:26557704 | T | A | 1 | a0001c0002t0019 | 1 | NA20300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-224T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/10 | 84567 | chr13 | 26557704 | ||||||
| chr13:26557719 | C | T | 1 | a0004c0008t0036 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-209C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/10 | 84552 | chr13 | 26557719 | ||||||
| chr13:26557746 | CCGGGCGG others(11): Show |
C | 1 | a0001c0001t0014 | 2 | HG02027.hp2 NA18946.hp1 |
5_prime_UTR_variant | MODIFIER | c.-177_-160delCGGCCG others(12): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/10 | 84503 | INFO_REALIGN_3_PRIME | chr13 | 26557746 | |||||
| chr13:26557761 | G | A | 1 | a0001c0001t0020 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-167G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/10 | 84510 | chr13 | 26557761 | ||||||
| chr13:26685905 | C | T | 1 | a0001c0002t0035 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 60 | chr13 | 26685905 | ||||||
| chr13:26686035 | A | G | 3 | a0001c0001t0032 a0001c0001t0033 a0001c0001t0034 |
3 | NA19001.hp2 NA19064.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*190A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 190 | chr13 | 26686035 | ||||||
| chr13:26686128 | A | C | 1 | a0001c0002t0031 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*283A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 283 | chr13 | 26686128 | ||||||
| chr13:26686249 | A | G | 1 | a0001c0002t0030 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 404 | chr13 | 26686249 | ||||||
| chr13:26686263 | T | C | 1 | a0001c0001t0020 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*418T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 418 | chr13 | 26686263 | ||||||
| chr13:26686429 | C | T | 1 | a0001c0001t0029 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*584C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 584 | chr13 | 26686429 | ||||||
| chr13:26686452 | A | G | 13 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0006 others(10): Show |
64 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*607A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 607 | chr13 | 26686452 | ||||||
| chr13:26686464 | G | A | 1 | a0002c0003t0027 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*619G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 619 | chr13 | 26686464 | ||||||
| chr13:26686572 | C | G | 4 | a0001c0002t0009 a0001c0002t0025 a0001c0002t0026 others(1): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*727C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 727 | chr13 | 26686572 | ||||||
| chr13:26686694 | C | T | 5 | a0001c0002t0004 a0001c0002t0017 a0001c0002t0018 others(2): Show |
23 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*849C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 849 | chr13 | 26686694 | ||||||
| chr13:26686737 | GGAGCCCT others(16): Show |
G | 13 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0006 others(10): Show |
64 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*895_*917delGCCCTG others(17): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 895 | INFO_REALIGN_3_PRIME | chr13 | 26686737 | |||||
| chr13:26686777 | G | A | 12 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0012 others(9): Show |
108 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*932G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 932 | chr13 | 26686777 | ||||||
| chr13:26686941 | T | C | 1 | a0001c0001t0038 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1096T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1096 | chr13 | 26686941 | ||||||
| chr13:26687058 | T | C | 18 | a0001c0001t0021 a0001c0002t0003 a0001c0002t0004 others(15): Show |
75 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1213T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1213 | chr13 | 26687058 | ||||||
| chr13:26687194 | C | G | 1 | a0001c0001t0022 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1349C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1349 | chr13 | 26687194 | ||||||
| chr13:26687233 | A | C | 1 | a0001c0001t0034 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1388A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1388 | chr13 | 26687233 | ||||||
| chr13:26687236 | C | T | 1 | a0001c0001t0012 | 4 | HG01168.hp1 HG01496.hp2 HG01934.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1391C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1391 | chr13 | 26687236 | ||||||
| chr13:26687310 | G | A | 1 | a0001c0002t0016 | 2 | HG00738.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1465G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1465 | chr13 | 26687310 | ||||||
| chr13:26687382 | T | G | 1 | a0001c0001t0034 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1537T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1537 | chr13 | 26687382 | ||||||
| chr13:26687420 | G | A | 4 | a0001c0002t0004 a0001c0002t0017 a0001c0002t0018 others(1): Show |
22 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1575G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1575 | chr13 | 26687420 | ||||||
| chr13:26687709 | T | TTC | 4 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0023 others(1): Show |
16 | HG02074.hp1 HG02602.hp1 HG02683.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1878_*1879dupCT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1880 | INFO_REALIGN_3_PRIME | chr13 | 26687709 | |||||
| chr13:26687721 | C | CT | 4 | a0001c0002t0018 a0001c0002t0028 a0001c0002t0030 others(1): Show |
5 | HG01175.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1877dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1878 | INFO_REALIGN_3_PRIME | chr13 | 26687721 | |||||
| chr13:26687721 | C | CTT | 1 | a0001c0002t0004 | 17 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1877_*1878insTT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1878 | INFO_REALIGN_3_PRIME | chr13 | 26687721 | |||||
| chr13:26687723 | C | CT | 5 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0038 others(2): Show |
87 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1892dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1893 | INFO_REALIGN_3_PRIME | chr13 | 26687723 | |||||
| chr13:26687723 | C | CTCT | 10 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0014 others(7): Show |
106 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1879_*1880insCTT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1880 | INFO_REALIGN_3_PRIME | chr13 | 26687723 | |||||
| chr13:26687723 | C | CTCTT | 3 | a0001c0001t0015 a0001c0002t0025 a0001c0004t0013 |
6 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1879_*1880insCTTT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1880 | INFO_REALIGN_3_PRIME | chr13 | 26687723 | |||||
| chr13:26687723 | C | T | 13 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0011 others(10): Show |
52 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1878C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 1878 | chr13 | 26687723 | ||||||
| chr13:26688009 | GTTAA | G | 3 | a0001c0001t0033 a0001c0004t0013 a0001c0004t0024 |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2167_*2170delAATT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 2167 | INFO_REALIGN_3_PRIME | chr13 | 26688009 | |||||
| chr13:26688275 | A | G | 1 | a0001c0001t0007 | 8 | HG02809.hp2 HG02818.hp2 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2430A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 2430 | chr13 | 26688275 | ||||||
| chr13:26688489 | G | T | 2 | a0001c0004t0013 a0001c0004t0024 |
4 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2644G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 2644 | chr13 | 26688489 | ||||||
| chr13:26688812 | T | A | 3 | a0001c0002t0011 a0001c0002t0019 a0002c0003t0011 |
6 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2967T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 2967 | chr13 | 26688812 | ||||||
| chr13:26688835 | A | T | 1 | a0001c0001t0020 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2990A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 2990 | chr13 | 26688835 | ||||||
| chr13:26688938 | C | T | 2 | a0001c0004t0013 a0001c0004t0024 |
4 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3093C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 10/10 | 3093 | chr13 | 26688938 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:26557834 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0253 a0001c0001t0002g0272 others(38): Show |
42 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-109+15C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26557834 | |||||||
| chr13:26557840 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+21C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26557840 | |||||||
| chr13:26558019 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-109+200T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558019 | |||||||
| chr13:26558066 | G | C | 1 | a0001c0002t0009g0003 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-109+247G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558066 | |||||||
| chr13:26558186 | C | T | 20 | a0001c0001t0002g0239 a0001c0002t0004g0223 a0001c0002t0004g0224 others(17): Show |
20 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.-109+367C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558186 | |||||||
| chr13:26558205 | A | G | 1 | a0001c0001t0037g0292 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-109+386A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558205 | |||||||
| chr13:26558215 | C | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(11): Show |
14 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-109+396C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558215 | |||||||
| chr13:26558224 | G | C | 6 | a0001c0001t0008g0019 a0001c0002t0004g0021 a0001c0002t0004g0022 others(3): Show |
6 | HG01175.hp1 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+405G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558224 | |||||||
| chr13:26558312 | G | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-109+493G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558312 | |||||||
| chr13:26558353 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-109+534G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558353 | |||||||
| chr13:26558428 | A | G | 4 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0010g0220 others(1): Show |
4 | HG01099.hp2 HG02602.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+609A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558428 | |||||||
| chr13:26558453 | CCGCGAGT others(30): Show |
C | 20 | a0001c0001t0002g0239 a0001c0002t0004g0223 a0001c0002t0004g0224 others(17): Show |
20 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.-109+639_-109+675d others(39): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26558453 | ||||||
| chr13:26558499 | A | G | 25 | a0001c0001t0002g0239 a0001c0002t0004g0223 a0001c0002t0004g0224 others(22): Show |
25 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.-109+680A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558499 | |||||||
| chr13:26558507 | C | T | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.-109+688C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558507 | |||||||
| chr13:26558620 | A | G | 1 | a0001c0001t0034g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-109+801A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558620 | |||||||
| chr13:26558736 | G | C | 1 | a0001c0001t0020g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-109+917G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558736 | |||||||
| chr13:26558815 | T | G | 1 | a0001c0002t0028g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-109+996T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558815 | |||||||
| chr13:26558830 | G | C | 1 | a0001c0001t0010g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-109+1011G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26558830 | |||||||
| chr13:26559188 | A | C | 21 | a0001c0001t0002g0002 a0001c0001t0002g0272 a0001c0001t0002g0273 others(18): Show |
22 | HG00741.hp2 HG01261.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.-109+1369A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559188 | |||||||
| chr13:26559197 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-109+1378C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559197 | |||||||
| chr13:26559215 | G | A | 2 | a0001c0001t0002g0028 a0001c0001t0002g0029 |
2 | HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-109+1396G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559215 | |||||||
| chr13:26559380 | T | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+1561T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559380 | |||||||
| chr13:26559398 | A | C | 1 | a0001c0002t0028g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-109+1579A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559398 | |||||||
| chr13:26559414 | T | G | 1 | a0001c0002t0006g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-109+1595T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559414 | |||||||
| chr13:26559450 | A | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0253 a0001c0001t0002g0272 others(38): Show |
42 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-109+1631A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559450 | |||||||
| chr13:26559694 | A | T | 1 | a0002c0003t0003g0201 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-109+1875A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559694 | |||||||
| chr13:26559785 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+1966T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559785 | |||||||
| chr13:26559787 | C | CTT | 3 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0200 |
3 | HG01168.hp2 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-109+1971_-109+197 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559787 | ||||||
| chr13:26559788 | T | TTTTCTTT others(6): Show |
2 | a0001c0002t0006g0213 a0001c0004t0013g0197 |
2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-109+1976_-109+197 others(17): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559788 | ||||||
| chr13:26559788 | T | TTTTCTTT others(10): Show |
1 | a0001c0004t0024g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-109+1976_-109+197 others(21): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559788 | ||||||
| chr13:26559788 | T | TTTTCTTT others(22): Show |
2 | a0001c0002t0004g0238 a0001c0004t0013g0195 |
2 | NA18954.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-109+1976_-109+197 others(33): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559788 | ||||||
| chr13:26559788 | T | TTTTCTTT others(46): Show |
1 | a0001c0002t0004g0237 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-109+1976_-109+197 others(57): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559788 | ||||||
| chr13:26559788 | T | TTTTCTTT others(54): Show |
1 | a0001c0002t0004g0236 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-109+1976_-109+197 others(65): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559788 | ||||||
| chr13:26559788 | T | TTTTCTTT others(138): Show |
1 | a0001c0002t0004g0235 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-109+1976_-109+197 others(149): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559788 | ||||||
| chr13:26559788 | T | TTTTCTTT others(11): Show |
2 | a0001c0002t0011g0215 a0001c0002t0011g0216 |
2 | HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-109+1976_-109+197 others(22): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559788 | ||||||
| chr13:26559788 | T | TTTTCTTT others(31): Show |
1 | a0001c0002t0004g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-109+1976_-109+197 others(42): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559788 | ||||||
| chr13:26559788 | T | TTTTCTTT others(35): Show |
1 | a0001c0002t0004g0240 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-109+1976_-109+197 others(46): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559788 | ||||||
| chr13:26559788 | T | TTTTCTTT others(47): Show |
1 | a0001c0001t0002g0239 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-109+1976_-109+197 others(58): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559788 | ||||||
| chr13:26559788 | T | TTTTCTTT others(20): Show |
1 | a0001c0002t0019g0217 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-109+1976_-109+197 others(31): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559788 | ||||||
| chr13:26559792 | C | CT | 15 | a0001c0001t0001g0036 a0001c0002t0004g0223 a0001c0002t0004g0224 others(12): Show |
15 | HG01069.hp2 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.-109+1976dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559792 | ||||||
| chr13:26559804 | C | CT | 20 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(17): Show |
20 | HG00280.hp2 HG00408.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-109+1988dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559804 | ||||||
| chr13:26559804 | C | CTT | 4 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
4 | HG01109.hp1 HG01175.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+1987_-109+198 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559804 | ||||||
| chr13:26559804 | CTTTCTTT others(3): Show |
C | 4 | a0001c0001t0012g0191 a0001c0001t0012g0192 a0001c0001t0012g0193 others(1): Show |
4 | HG01168.hp1 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+1989_-109+199 others(14): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559804 | ||||||
| chr13:26559804 | CTTTCTTT others(10): Show |
C | 1 | a0001c0001t0001g0190 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-109+1989_-109+200 others(21): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559804 | ||||||
| chr13:26559804 | CTTTCTTT others(11): Show |
C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | NA18977.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-109+1989_-109+200 others(22): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559804 | ||||||
| chr13:26559804 | CTTTCTTT others(12): Show |
C | 1 | a0001c0001t0001g0187 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-109+1989_-109+200 others(23): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559804 | ||||||
| chr13:26559806 | TTC | T | 6 | a0001c0002t0003g0152 a0001c0002t0009g0205 a0001c0002t0009g0207 others(3): Show |
6 | HG02735.hp1 HG03225.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+1989_-109+199 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559806 | ||||||
| chr13:26559807 | TC | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0109 a0001c0001t0001g0111 others(32): Show |
35 | HG00558.hp1 HG00673.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.-109+1989delC | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559807 | |||||||
| chr13:26559808 | C | CT | 11 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0280 others(8): Show |
11 | HG01515.hp2 HG01516.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.-109+2015dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559808 | ||||||
| chr13:26559808 | C | CTT | 6 | a0001c0001t0002g0253 a0001c0001t0005g0259 a0001c0001t0005g0260 others(3): Show |
6 | HG01255.hp1 HG01256.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+2014_-109+201 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559808 | ||||||
| chr13:26559808 | C | T | 57 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(54): Show |
57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.-109+1989C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559808 | |||||||
| chr13:26559808 | CTT | C | 11 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0002g0200 others(8): Show |
11 | HG01192.hp2 HG01891.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.-109+2014_-109+201 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559808 | ||||||
| chr13:26559808 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0007g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-109+2006_-109+201 others(14): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559808 | ||||||
| chr13:26559809 | T | TTTC | 11 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0092 others(8): Show |
11 | HG00408.hp1 HG00673.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.-109+1992_-109+199 others(7): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559809 | ||||||
| chr13:26559809 | T | TTTCTTTC others(8): Show |
1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-109+1992_-109+199 others(19): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559809 | ||||||
| chr13:26559809 | T | TTTCTTTC others(24): Show |
1 | a0001c0002t0004g0223 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-109+1992_-109+199 others(35): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559809 | ||||||
| chr13:26559809 | T | TTTCTTTC others(32): Show |
1 | a0001c0002t0004g0224 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-109+1992_-109+199 others(43): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559809 | ||||||
| chr13:26559809 | T | TTTCTTTC others(32): Show |
4 | a0001c0002t0004g0231 a0001c0002t0004g0233 a0001c0002t0017g0232 others(1): Show |
4 | HG01081.hp1 HG01099.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+1992_-109+199 others(43): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559809 | ||||||
| chr13:26559809 | T | TTTCTTTC others(36): Show |
1 | a0001c0002t0004g0230 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-109+1992_-109+199 others(47): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559809 | ||||||
| chr13:26559809 | T | TTTCTTTC others(44): Show |
1 | a0001c0002t0004g0228 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-109+1992_-109+199 others(55): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559809 | ||||||
| chr13:26559809 | T | TTTCTTTC others(48): Show |
1 | a0001c0002t0004g0226 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-109+1992_-109+199 others(59): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559809 | ||||||
| chr13:26559809 | T | TTTCTTTC others(248): Show |
1 | a0001c0002t0004g0225 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-109+1992_-109+199 others(259): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559809 | ||||||
| chr13:26559810 | T | TTC | 50 | a0001c0001t0001g0009 a0001c0001t0002g0024 a0001c0001t0002g0028 others(47): Show |
50 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.-109+1992_-109+199 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559810 | ||||||
| chr13:26559810 | T | TTCTTTC | 7 | a0001c0001t0002g0039 a0001c0001t0002g0041 a0001c0001t0002g0042 others(4): Show |
7 | HG00099.hp2 NA18906.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+1992_-109+199 others(10): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559810 | ||||||
| chr13:26559810 | T | TTCTTTCT others(15): Show |
1 | a0001c0001t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-109+1992_-109+199 others(26): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559810 | ||||||
| chr13:26559810 | T | TTCTTTCT others(35): Show |
3 | a0001c0002t0006g0031 a0001c0002t0017g0229 a0001c0004t0013g0033 |
3 | HG01515.hp1 HG02148.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-109+1992_-109+199 others(46): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559810 | ||||||
| chr13:26559810 | T | TTCTTTCT others(43): Show |
1 | a0001c0002t0030g0227 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-109+1992_-109+199 others(54): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26559810 | ||||||
| chr13:26559811 | T | TC | 16 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(13): Show |
16 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-109+1992_-109+199 others(5): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559811 | |||||||
| chr13:26559811 | T | TCTTTCTT others(10): Show |
1 | a0001c0002t0006g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-109+1992_-109+199 others(21): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559811 | |||||||
| chr13:26559811 | T | TCTTTCTT others(26): Show |
1 | a0001c0002t0006g0034 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-109+1992_-109+199 others(37): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559811 | |||||||
| chr13:26559811 | T | TCTTTCTT others(30): Show |
1 | a0001c0002t0006g0032 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-109+1992_-109+199 others(41): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559811 | |||||||
| chr13:26559811 | T | TCTTTCTT others(42): Show |
1 | a0001c0002t0006g0030 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-109+1992_-109+199 others(53): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559811 | |||||||
| chr13:26559812 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0002g0096 a0001c0001t0002g0239 others(6): Show |
9 | HG00544.hp2 HG02129.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+1993T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559812 | |||||||
| chr13:26559813 | T | C | 22 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0092 others(19): Show |
22 | HG00408.hp1 HG00673.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-109+1994T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559813 | |||||||
| chr13:26559814 | T | C | 72 | a0001c0001t0001g0036 a0001c0001t0001g0102 a0001c0001t0001g0103 others(69): Show |
72 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-109+1995T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559814 | |||||||
| chr13:26559815 | T | C | 13 | a0001c0001t0001g0108 a0001c0001t0002g0046 a0001c0001t0021g0004 others(10): Show |
13 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.-109+1996T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559815 | |||||||
| chr13:26559816 | T | C | 8 | a0001c0001t0002g0096 a0001c0001t0002g0239 a0001c0002t0004g0238 others(5): Show |
8 | HG00544.hp2 HG02129.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-109+1997T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559816 | |||||||
| chr13:26559817 | T | C | 22 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0092 others(19): Show |
22 | HG00408.hp1 HG00673.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-109+1998T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559817 | |||||||
| chr13:26559818 | T | C | 72 | a0001c0001t0001g0036 a0001c0001t0001g0102 a0001c0001t0001g0103 others(69): Show |
72 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-109+1999T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559818 | |||||||
| chr13:26559819 | T | C | 12 | a0001c0001t0001g0108 a0001c0001t0002g0046 a0001c0002t0003g0037 others(9): Show |
12 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-109+2000T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559819 | |||||||
| chr13:26559820 | T | C | 1 | a0001c0004t0013g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-109+2001T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559820 | |||||||
| chr13:26559821 | T | C | 1 | a0001c0002t0004g0225 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-109+2002T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559821 | |||||||
| chr13:26559822 | T | C | 2 | a0001c0002t0006g0031 a0001c0002t0017g0229 |
2 | HG01515.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-109+2003T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559822 | |||||||
| chr13:26559823 | T | C | 8 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0006g0030 others(5): Show |
8 | HG01074.hp1 HG01192.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-109+2004T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559823 | |||||||
| chr13:26559826 | T | C | 1 | a0001c0002t0006g0031 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-109+2007T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559826 | |||||||
| chr13:26559920 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-109+2101C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559920 | |||||||
| chr13:26559976 | C | T | 1 | a0001c0002t0004g0238 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-109+2157C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26559976 | |||||||
| chr13:26560108 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-109+2289C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560108 | |||||||
| chr13:26560159 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-109+2340T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560159 | |||||||
| chr13:26560177 | C | CT | 6 | a0001c0001t0012g0194 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01168.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+2365dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26560177 | ||||||
| chr13:26560222 | A | T | 19 | a0001c0001t0005g0254 a0001c0001t0005g0255 a0001c0001t0005g0256 others(16): Show |
19 | HG00639.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-109+2403A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560222 | |||||||
| chr13:26560276 | T | C | 1 | a0001c0001t0037g0292 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-109+2457T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560276 | |||||||
| chr13:26560389 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 |
3 | HG01109.hp2 HG02145.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-109+2570C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560389 | |||||||
| chr13:26560414 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0109 a0001c0001t0001g0111 others(96): Show |
99 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-109+2595A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560414 | |||||||
| chr13:26560438 | A | AAT | 4 | a0001c0002t0006g0213 a0001c0002t0011g0215 a0001c0002t0011g0216 others(1): Show |
4 | HG02622.hp1 HG03579.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+2623_-109+262 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26560438 | ||||||
| chr13:26560488 | A | G | 5 | a0001c0002t0016g0010 a0001c0002t0016g0014 a0002c0003t0011g0011 others(2): Show |
5 | HG00738.hp2 HG02109.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-109+2669A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560488 | |||||||
| chr13:26560535 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-109+2716G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560535 | |||||||
| chr13:26560544 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+2725T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560544 | |||||||
| chr13:26560640 | G | A | 1 | a0001c0002t0006g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-109+2821G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560640 | |||||||
| chr13:26560654 | T | A | 2 | a0001c0002t0006g0034 a0001c0002t0006g0035 |
2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-109+2835T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560654 | |||||||
| chr13:26560679 | G | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+2860G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560679 | |||||||
| chr13:26560890 | G | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+3071G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560890 | |||||||
| chr13:26560933 | A | G | 1 | a0001c0001t0005g0271 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-109+3114A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26560933 | |||||||
| chr13:26561031 | A | G | 18 | a0001c0001t0001g0108 a0001c0001t0002g0282 a0001c0001t0002g0283 others(15): Show |
18 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(15): Show |
intron_variant | MODIFIER | c.-109+3212A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561031 | |||||||
| chr13:26561052 | A | G | 3 | a0001c0001t0008g0249 a0001c0001t0008g0250 a0002c0003t0027g0104 |
3 | HG02257.hp1 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-109+3233A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561052 | |||||||
| chr13:26561138 | T | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.-109+3319T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561138 | |||||||
| chr13:26561144 | G | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+3325G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561144 | |||||||
| chr13:26561207 | A | T | 1 | a0001c0001t0005g0270 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-109+3388A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561207 | |||||||
| chr13:26561229 | C | G | 8 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 others(5): Show |
8 | HG00738.hp2 HG01109.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-109+3410C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561229 | |||||||
| chr13:26561351 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-109+3532T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561351 | |||||||
| chr13:26561389 | C | G | 4 | a0001c0002t0016g0014 a0002c0003t0011g0011 a0002c0003t0011g0012 others(1): Show |
4 | HG00738.hp2 HG02109.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+3570C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561389 | |||||||
| chr13:26561493 | G | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(1): Show |
4 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+3674G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561493 | |||||||
| chr13:26561518 | G | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+3699G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561518 | |||||||
| chr13:26561538 | C | G | 1 | a0001c0002t0006g0246 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-109+3719C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561538 | |||||||
| chr13:26561581 | C | T | 1 | a0003c0005t0008g0252 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-109+3762C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561581 | |||||||
| chr13:26561619 | A | G | 2 | a0001c0002t0003g0037 a0001c0002t0003g0038 |
2 | HG01074.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-109+3800A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561619 | |||||||
| chr13:26561748 | T | C | 8 | a0001c0002t0006g0213 a0001c0002t0006g0242 a0001c0002t0006g0243 others(5): Show |
8 | HG02258.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-109+3929T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561748 | |||||||
| chr13:26561875 | G | C | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.-109+4056G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561875 | |||||||
| chr13:26561921 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(100): Show |
103 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-109+4102A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26561921 | |||||||
| chr13:26562219 | G | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+4400G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562219 | |||||||
| chr13:26562452 | C | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(110): Show |
113 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-109+4633C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562452 | |||||||
| chr13:26562523 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+4704A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562523 | |||||||
| chr13:26562623 | T | C | 1 | a0001c0001t0012g0191 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-109+4804T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562623 | |||||||
| chr13:26562857 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-109+5038T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562857 | |||||||
| chr13:26562857 | T | TCCTCCCC others(14): Show |
1 | a0001c0001t0002g0028 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-109+5048_-109+504 others(25): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26562857 | ||||||
| chr13:26562857 | T | TCCTCCCC others(8): Show |
143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
143 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.-109+5048_-109+504 others(19): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26562857 | ||||||
| chr13:26562857 | T | TCCTCCCC others(13): Show |
87 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0036 others(84): Show |
87 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-109+5048_-109+504 others(24): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26562857 | ||||||
| chr13:26562857 | T | TCCTCCCC others(18): Show |
4 | a0002c0003t0003g0049 a0002c0003t0003g0050 a0002c0003t0003g0051 others(1): Show |
4 | HG00423.hp1 HG02080.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+5048_-109+504 others(29): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26562857 | ||||||
| chr13:26562859 | C | CTCCCCTC others(3): Show |
2 | a0001c0001t0002g0046 a0001c0001t0002g0200 |
2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-109+5048_-109+504 others(14): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26562859 | ||||||
| chr13:26562860 | T | TCCCCTCC others(14): Show |
1 | a0002c0003t0003g0048 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-109+5048_-109+504 others(25): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26562860 | ||||||
| chr13:26562863 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-109+5044C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562863 | |||||||
| chr13:26562865 | T | TCCCCTCC others(17): Show |
1 | a0001c0002t0006g0107 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-109+5048_-109+504 others(28): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26562865 | ||||||
| chr13:26562868 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+5049T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562868 | |||||||
| chr13:26562876 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+5057T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562876 | |||||||
| chr13:26562883 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+5064T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562883 | |||||||
| chr13:26562884 | C | CCCCTTT | 238 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.-109+5065_-109+506 others(10): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562884 | |||||||
| chr13:26562884 | C | T | 2 | a0001c0001t0001g0112 a0001c0002t0006g0107 |
2 | HG00673.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-109+5065C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562884 | |||||||
| chr13:26562885 | G | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+5066G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562885 | |||||||
| chr13:26562906 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+5087T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562906 | |||||||
| chr13:26562907 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+5088T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562907 | |||||||
| chr13:26562910 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+5091C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26562910 | |||||||
| chr13:26562952 | C | CT | 9 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0006g0030 others(6): Show |
9 | HG01074.hp1 HG01192.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+5141dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26562952 | ||||||
| chr13:26563142 | C | A | 2 | a0001c0001t0001g0036 a0001c0004t0024g0196 |
2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-109+5323C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563142 | |||||||
| chr13:26563155 | G | A | 63 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(60): Show |
63 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-109+5336G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563155 | |||||||
| chr13:26563202 | A | G | 3 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 |
3 | HG02717.hp2 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-109+5383A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563202 | |||||||
| chr13:26563206 | G | A | 3 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 |
3 | HG02717.hp2 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-109+5387G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563206 | |||||||
| chr13:26563210 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-109+5391A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563210 | |||||||
| chr13:26563248 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.-109+5429T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563248 | |||||||
| chr13:26563323 | G | A | 7 | a0001c0002t0006g0030 a0001c0002t0006g0031 a0001c0002t0006g0032 others(4): Show |
7 | HG01192.hp1 HG02148.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+5504G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563323 | |||||||
| chr13:26563338 | C | T | 2 | a0001c0001t0010g0027 a0001c0001t0022g0168 |
2 | HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-109+5519C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563338 | |||||||
| chr13:26563491 | C | A | 7 | a0001c0002t0006g0030 a0001c0002t0006g0031 a0001c0002t0006g0032 others(4): Show |
7 | HG01192.hp1 HG02148.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+5672C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563491 | |||||||
| chr13:26563654 | C | CA | 36 | a0001c0001t0001g0036 a0001c0001t0002g0053 a0001c0001t0002g0170 others(33): Show |
36 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.-109+5859dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26563654 | ||||||
| chr13:26563654 | C | CAA | 21 | a0001c0001t0001g0167 a0001c0001t0002g0002 a0001c0001t0002g0253 others(18): Show |
22 | HG00735.hp2 HG01070.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.-109+5858_-109+585 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26563654 | ||||||
| chr13:26563654 | C | CAAA | 82 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.-109+5857_-109+585 others(7): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26563654 | ||||||
| chr13:26563654 | C | CAAAA | 21 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(18): Show |
21 | HG00544.hp1 HG01109.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.-109+5856_-109+585 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26563654 | ||||||
| chr13:26563654 | CA | C | 8 | a0001c0001t0002g0043 a0001c0001t0002g0082 a0001c0001t0002g0083 others(5): Show |
8 | HG01074.hp2 HG01109.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.-109+5859delA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26563654 | ||||||
| chr13:26563654 | CAA | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(12): Show |
15 | HG00639.hp2 HG00738.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-109+5858_-109+585 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26563654 | ||||||
| chr13:26563680 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+5861A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563680 | |||||||
| chr13:26563730 | G | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+5911G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563730 | |||||||
| chr13:26563767 | TCTC | T | 3 | a0001c0002t0006g0030 a0001c0002t0006g0031 a0001c0002t0006g0032 |
3 | HG02148.hp1 HG02486.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-109+5949_-109+595 others(7): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563767 | |||||||
| chr13:26563777 | A | AT | 4 | a0001c0002t0006g0213 a0001c0002t0011g0215 a0001c0002t0011g0216 others(1): Show |
4 | HG02622.hp1 HG03579.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+5960dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26563777 | ||||||
| chr13:26563791 | C | CT | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(10): Show |
13 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-109+5985dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26563791 | ||||||
| chr13:26563804 | T | A | 1 | a0001c0002t0004g0235 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-109+5985T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563804 | |||||||
| chr13:26563805 | A | T | 16 | a0001c0001t0002g0239 a0001c0001t0002g0277 a0001c0001t0002g0278 others(13): Show |
16 | HG00544.hp2 HG01433.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.-109+5986A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563805 | |||||||
| chr13:26563822 | A | G | 5 | a0001c0001t0001g0166 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG00280.hp2 HG01109.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-109+6003A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563822 | |||||||
| chr13:26563852 | A | T | 1 | a0001c0002t0011g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-109+6033A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563852 | |||||||
| chr13:26563917 | A | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(11): Show |
14 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-109+6098A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26563917 | |||||||
| chr13:26564252 | A | G | 82 | a0001c0001t0001g0108 a0001c0001t0002g0024 a0001c0001t0002g0028 others(79): Show |
82 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-109+6433A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26564252 | |||||||
| chr13:26564335 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
128 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-109+6516C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26564335 | |||||||
| chr13:26564558 | A | G | 19 | a0001c0001t0002g0239 a0001c0002t0004g0223 a0001c0002t0004g0224 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-109+6739A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26564558 | |||||||
| chr13:26564885 | C | T | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+7066C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26564885 | |||||||
| chr13:26564900 | G | GT | 105 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(102): Show |
105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-109+7104dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26564900 | ||||||
| chr13:26564900 | G | GTT | 44 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0116 others(41): Show |
44 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-109+7103_-109+710 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26564900 | ||||||
| chr13:26564900 | G | GTTT | 13 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0163 others(10): Show |
13 | HG00741.hp1 HG01123.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.-109+7102_-109+710 others(7): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26564900 | ||||||
| chr13:26564900 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-109+7081G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26564900 | |||||||
| chr13:26564900 | GT | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0002g0198 others(10): Show |
13 | HG00738.hp2 HG01169.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-109+7104delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26564900 | ||||||
| chr13:26565174 | G | A | 1 | a0001c0002t0026g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-109+7355G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565174 | |||||||
| chr13:26565185 | G | GA | 69 | a0001c0001t0001g0036 a0001c0001t0001g0112 a0001c0001t0001g0120 others(66): Show |
70 | HG00423.hp2 HG00642.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.-109+7380dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26565185 | ||||||
| chr13:26565185 | G | GAA | 173 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
173 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-109+7379_-109+738 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26565185 | ||||||
| chr13:26565185 | G | GAAA | 27 | a0001c0001t0001g0111 a0001c0001t0001g0147 a0001c0001t0002g0054 others(24): Show |
27 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.-109+7378_-109+738 others(7): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26565185 | ||||||
| chr13:26565382 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-109+7563G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565382 | |||||||
| chr13:26565507 | C | A | 4 | a0001c0002t0006g0213 a0001c0002t0011g0215 a0001c0002t0011g0216 others(1): Show |
4 | HG02622.hp1 HG03579.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+7688C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565507 | |||||||
| chr13:26565519 | G | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+7700G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565519 | |||||||
| chr13:26565520 | A | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+7701A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565520 | |||||||
| chr13:26565569 | T | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-109+7750T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565569 | |||||||
| chr13:26565648 | T | A | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.-109+7829T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565648 | |||||||
| chr13:26565663 | T | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+7844T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565663 | |||||||
| chr13:26565677 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(101): Show |
104 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-109+7858A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565677 | |||||||
| chr13:26565691 | G | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+7872G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565691 | |||||||
| chr13:26565739 | T | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(237): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.-109+7920T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565739 | |||||||
| chr13:26565790 | T | G | 1 | a0001c0002t0011g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-109+7971T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565790 | |||||||
| chr13:26565875 | A | C | 1 | a0001c0001t0002g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-109+8056A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565875 | |||||||
| chr13:26565953 | A | G | 9 | a0001c0001t0001g0119 a0001c0001t0001g0144 a0001c0001t0001g0145 others(6): Show |
9 | HG02027.hp1 HG02056.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.-109+8134A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26565953 | |||||||
| chr13:26566018 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-109+8199G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26566018 | |||||||
| chr13:26566371 | A | G | 2 | a0001c0002t0011g0215 a0001c0002t0011g0216 |
2 | HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-109+8552A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26566371 | |||||||
| chr13:26566814 | A | G | 2 | a0001c0001t0005g0268 a0001c0001t0005g0269 |
2 | HG01081.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-109+8995A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26566814 | |||||||
| chr13:26566838 | A | G | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+9019A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26566838 | |||||||
| chr13:26566969 | A | G | 1 | a0001c0001t0008g0248 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-109+9150A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26566969 | |||||||
| chr13:26567326 | T | C | 4 | a0001c0002t0009g0205 a0001c0002t0009g0208 a0001c0002t0009g0209 others(1): Show |
4 | HG02145.hp1 HG03195.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+9507T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26567326 | |||||||
| chr13:26567339 | C | T | 1 | a0001c0002t0003g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-109+9520C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26567339 | |||||||
| chr13:26567417 | G | C | 5 | a0001c0002t0016g0010 a0001c0002t0016g0014 a0002c0003t0011g0011 others(2): Show |
5 | HG00738.hp2 HG02109.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-109+9598G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26567417 | |||||||
| chr13:26567473 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+9654T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26567473 | |||||||
| chr13:26567562 | T | C | 1 | a0001c0001t0002g0284 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-109+9743T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26567562 | |||||||
| chr13:26567693 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-109+9874G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26567693 | |||||||
| chr13:26567698 | TA | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
132 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-109+9889delA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26567698 | ||||||
| chr13:26567698 | TAA | T | 10 | a0001c0001t0008g0019 a0001c0001t0020g0026 a0001c0002t0006g0034 others(7): Show |
10 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-109+9888_-109+988 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26567698 | ||||||
| chr13:26567705 | A | T | 20 | a0001c0001t0001g0036 a0001c0001t0002g0239 a0001c0002t0004g0223 others(17): Show |
20 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.-109+9886A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26567705 | |||||||
| chr13:26567707 | A | AAT | 7 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0085 others(4): Show |
7 | HG01496.hp1 HG02818.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+9902_-109+990 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26567707 | ||||||
| chr13:26567707 | A | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-109+9888A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26567707 | |||||||
| chr13:26567709 | T | A | 3 | a0001c0002t0006g0030 a0001c0002t0006g0032 a0001c0002t0011g0215 |
3 | HG02486.hp2 HG02622.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-109+9890T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26567709 | |||||||
| chr13:26567711 | T | A | 1 | a0001c0002t0011g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-109+9892T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26567711 | |||||||
| chr13:26567804 | C | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-109+9985C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26567804 | |||||||
| chr13:26567829 | A | G | 20 | a0001c0001t0002g0239 a0001c0002t0004g0223 a0001c0002t0004g0224 others(17): Show |
20 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.-109+10010A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26567829 | |||||||
| chr13:26568153 | T | G | 112 | a0001c0001t0001g0036 a0001c0001t0001g0108 a0001c0001t0002g0024 others(109): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-109+10334T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26568153 | |||||||
| chr13:26568258 | A | C | 3 | a0001c0001t0002g0239 a0001c0002t0004g0240 a0001c0002t0004g0241 |
3 | HG00544.hp2 NA18999.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-109+10439A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26568258 | |||||||
| chr13:26568293 | T | C | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.-109+10474T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26568293 | |||||||
| chr13:26568356 | C | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+10537C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26568356 | |||||||
| chr13:26568366 | T | C | 4 | a0001c0002t0009g0205 a0001c0002t0009g0208 a0001c0002t0009g0209 others(1): Show |
4 | HG02145.hp1 HG03195.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+10547T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26568366 | |||||||
| chr13:26568923 | G | C | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-109+11104G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26568923 | |||||||
| chr13:26569246 | CAATT | C | 6 | a0001c0002t0006g0213 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02886.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+11431_-109+11 others(10): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26569246 | ||||||
| chr13:26569381 | C | T | 2 | a0001c0002t0004g0234 a0001c0002t0030g0227 |
2 | HG01433.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-109+11562C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26569381 | |||||||
| chr13:26569473 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+11654C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26569473 | |||||||
| chr13:26569568 | C | G | 7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0014g0118 others(4): Show |
7 | HG02027.hp2 HG02083.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+11749C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26569568 | |||||||
| chr13:26569631 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(237): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.-109+11812A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26569631 | |||||||
| chr13:26569645 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-109+11826A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26569645 | |||||||
| chr13:26569651 | A | G | 10 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0137 others(7): Show |
10 | HG00408.hp2 HG01070.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.-109+11832A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26569651 | |||||||
| chr13:26569778 | A | G | 6 | a0001c0002t0006g0213 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02886.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+11959A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26569778 | |||||||
| chr13:26569886 | G | A | 1 | a0001c0002t0028g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-109+12067G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26569886 | |||||||
| chr13:26570060 | C | T | 64 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(61): Show |
64 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-109+12241C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26570060 | |||||||
| chr13:26570076 | A | T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0073 |
2 | HG01256.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-109+12257A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26570076 | |||||||
| chr13:26570157 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+12338A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26570157 | |||||||
| chr13:26570161 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-109+12342G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26570161 | |||||||
| chr13:26570225 | T | C | 1 | a0002c0003t0003g0056 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-109+12406T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26570225 | |||||||
| chr13:26570401 | T | C | 1 | a0001c0004t0024g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-109+12582T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26570401 | |||||||
| chr13:26570465 | T | TTCTAGTT others(195): Show |
1 | a0001c0002t0011g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-109+12659_-109+12 others(208): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26570465 | ||||||
| chr13:26570682 | C | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-109+12863C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26570682 | |||||||
| chr13:26570733 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+12914A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26570733 | |||||||
| chr13:26570756 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(8): Show |
11 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-109+12937A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26570756 | |||||||
| chr13:26570875 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(111): Show |
114 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-109+13056G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26570875 | |||||||
| chr13:26570910 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-109+13091T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26570910 | |||||||
| chr13:26571275 | GCTTTT | G | 115 | a0001c0001t0001g0036 a0001c0001t0001g0108 a0001c0001t0002g0024 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.-109+13461_-109+13 others(11): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26571275 | ||||||
| chr13:26571382 | A | G | 1 | a0001c0002t0006g0031 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-109+13563A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26571382 | |||||||
| chr13:26571568 | T | C | 64 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(61): Show |
64 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-109+13749T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26571568 | |||||||
| chr13:26571578 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-109+13759C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26571578 | |||||||
| chr13:26571705 | C | CT | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+13890dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26571705 | ||||||
| chr13:26571948 | A | G | 2 | a0002c0003t0003g0099 a0002c0003t0003g0201 |
2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-109+14129A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26571948 | |||||||
| chr13:26572070 | G | A | 1 | a0001c0001t0023g0094 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-109+14251G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26572070 | |||||||
| chr13:26572098 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-109+14279G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26572098 | |||||||
| chr13:26572118 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-109+14299A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26572118 | |||||||
| chr13:26572192 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 |
3 | HG01109.hp2 HG02145.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-109+14373A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26572192 | |||||||
| chr13:26572312 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(111): Show |
114 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-109+14493C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26572312 | |||||||
| chr13:26572323 | C | T | 9 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0006g0030 others(6): Show |
9 | HG01074.hp1 HG01192.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+14504C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26572323 | |||||||
| chr13:26572692 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-109+14873A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26572692 | |||||||
| chr13:26572754 | T | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(8): Show |
11 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-109+14935T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26572754 | |||||||
| chr13:26572784 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-109+14965T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26572784 | |||||||
| chr13:26572844 | C | T | 2 | a0001c0001t0010g0027 a0001c0001t0022g0168 |
2 | HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-109+15025C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26572844 | |||||||
| chr13:26572867 | A | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0179 |
2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-109+15048A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26572867 | |||||||
| chr13:26572925 | G | T | 7 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0131 others(4): Show |
7 | HG02056.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+15106G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26572925 | |||||||
| chr13:26572951 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+15132T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26572951 | |||||||
| chr13:26573315 | C | A | 1 | a0001c0002t0035g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-109+15496C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26573315 | |||||||
| chr13:26573545 | T | C | 1 | a0001c0004t0024g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-109+15726T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26573545 | |||||||
| chr13:26573774 | G | A | 1 | a0001c0002t0004g0225 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-109+15955G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26573774 | |||||||
| chr13:26573907 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(8): Show |
11 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-109+16088A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26573907 | |||||||
| chr13:26573997 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-109+16178A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26573997 | |||||||
| chr13:26574198 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-109+16379C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26574198 | |||||||
| chr13:26574463 | G | C | 2 | a0001c0002t0003g0037 a0001c0002t0003g0038 |
2 | HG01074.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-109+16644G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26574463 | |||||||
| chr13:26574464 | A | AT | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG00544.hp2 HG00639.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-109+16655dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26574464 | ||||||
| chr13:26574565 | A | T | 1 | a0001c0002t0019g0217 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-109+16746A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26574565 | |||||||
| chr13:26574733 | T | A | 7 | a0001c0001t0005g0259 a0001c0001t0005g0260 a0001c0001t0005g0261 others(4): Show |
7 | HG01255.hp1 HG01256.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+16914T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26574733 | |||||||
| chr13:26574868 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-109+17049G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26574868 | |||||||
| chr13:26574982 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+17163A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26574982 | |||||||
| chr13:26575033 | A | T | 2 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
2 | NA19090.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-109+17214A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26575033 | |||||||
| chr13:26575037 | T | C | 2 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
2 | NA19090.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-109+17218T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26575037 | |||||||
| chr13:26575052 | G | C | 2 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
2 | NA19090.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-109+17233G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26575052 | |||||||
| chr13:26575097 | C | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+17278C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26575097 | |||||||
| chr13:26575100 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+17281C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26575100 | |||||||
| chr13:26575126 | G | A | 1 | a0001c0004t0013g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-109+17307G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26575126 | |||||||
| chr13:26575330 | A | G | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-109+17511A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26575330 | |||||||
| chr13:26575476 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-109+17657G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26575476 | |||||||
| chr13:26575625 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-109+17806A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26575625 | |||||||
| chr13:26575849 | G | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(8): Show |
11 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-109+18030G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26575849 | |||||||
| chr13:26575924 | G | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+18105G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26575924 | |||||||
| chr13:26576115 | C | T | 1 | a0001c0002t0003g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-109+18296C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576115 | |||||||
| chr13:26576205 | G | T | 6 | a0001c0002t0009g0003 a0001c0002t0009g0207 a0001c0002t0009g0211 others(3): Show |
6 | HG02055.hp1 HG03041.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+18386G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576205 | |||||||
| chr13:26576250 | A | G | 63 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(60): Show |
63 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-109+18431A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576250 | |||||||
| chr13:26576256 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-109+18437A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576256 | |||||||
| chr13:26576366 | G | A | 1 | a0001c0001t0005g0254 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-109+18547G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576366 | |||||||
| chr13:26576502 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-109+18683G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576502 | |||||||
| chr13:26576615 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+18796A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576615 | |||||||
| chr13:26576618 | T | C | 1 | a0002c0003t0003g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-109+18799T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576618 | |||||||
| chr13:26576665 | A | C | 5 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 others(2): Show |
5 | HG00738.hp2 HG01109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+18846A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576665 | |||||||
| chr13:26576731 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+18912A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576731 | |||||||
| chr13:26576738 | T | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(8): Show |
11 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-109+18919T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576738 | |||||||
| chr13:26576860 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-109+19041G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576860 | |||||||
| chr13:26576883 | A | G | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-109+19064A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576883 | |||||||
| chr13:26576911 | T | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(100): Show |
103 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-109+19092T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26576911 | |||||||
| chr13:26577033 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
125 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-109+19214A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577033 | |||||||
| chr13:26577054 | A | G | 7 | a0001c0002t0006g0213 a0001c0002t0011g0215 a0001c0002t0011g0216 others(4): Show |
7 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+19235A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577054 | |||||||
| chr13:26577114 | G | T | 1 | a0001c0002t0028g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-109+19295G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577114 | |||||||
| chr13:26577160 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-109+19341A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577160 | |||||||
| chr13:26577258 | A | T | 1 | a0001c0002t0028g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-109+19439A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577258 | |||||||
| chr13:26577269 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+19450A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577269 | |||||||
| chr13:26577287 | T | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+19468T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577287 | |||||||
| chr13:26577329 | C | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+19510C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577329 | |||||||
| chr13:26577443 | A | G | 1 | a0001c0001t0002g0072 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-109+19624A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577443 | |||||||
| chr13:26577471 | C | G | 2 | a0001c0004t0013g0033 a0001c0004t0013g0195 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-109+19652C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577471 | |||||||
| chr13:26577477 | A | G | 3 | a0001c0002t0006g0030 a0001c0002t0006g0031 a0001c0002t0006g0032 |
3 | HG02148.hp1 HG02486.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-109+19658A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577477 | |||||||
| chr13:26577481 | A | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+19662A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577481 | |||||||
| chr13:26577489 | A | G | 9 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0006g0030 others(6): Show |
9 | HG01074.hp1 HG01192.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+19670A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577489 | |||||||
| chr13:26577493 | A | G | 7 | a0001c0002t0006g0213 a0001c0002t0011g0215 a0001c0002t0011g0216 others(4): Show |
7 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+19674A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577493 | |||||||
| chr13:26577636 | A | G | 3 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 |
3 | HG02622.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-109+19817A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577636 | |||||||
| chr13:26577722 | G | GA | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+19914dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26577722 | ||||||
| chr13:26577730 | A | C | 2 | a0001c0002t0009g0207 a0001c0002t0009g0212 |
2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-109+19911A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26577730 | |||||||
| chr13:26578102 | T | C | 1 | a0001c0002t0017g0229 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-109+20283T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26578102 | |||||||
| chr13:26578390 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
125 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-109+20571G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26578390 | |||||||
| chr13:26578444 | A | C | 65 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(62): Show |
65 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-109+20625A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26578444 | |||||||
| chr13:26578467 | T | C | 1 | a0001c0001t0002g0053 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-109+20648T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26578467 | |||||||
| chr13:26578472 | C | T | 1 | a0001c0002t0016g0010 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-109+20653C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26578472 | |||||||
| chr13:26578512 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(111): Show |
114 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-109+20693C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26578512 | |||||||
| chr13:26578606 | C | T | 1 | a0001c0002t0009g0003 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-109+20787C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26578606 | |||||||
| chr13:26578665 | C | T | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-109+20846C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26578665 | |||||||
| chr13:26578969 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-109+21150C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26578969 | |||||||
| chr13:26578973 | A | G | 15 | a0001c0001t0002g0002 a0001c0001t0002g0273 a0001c0001t0002g0274 others(12): Show |
16 | HG00741.hp2 HG01261.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.-109+21154A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26578973 | |||||||
| chr13:26578993 | C | CT | 37 | a0001c0001t0002g0002 a0001c0001t0002g0272 a0001c0001t0002g0273 others(34): Show |
38 | HG00639.hp1 HG00735.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.-109+21197dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTT | 8 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0169 others(5): Show |
8 | HG00741.hp2 HG01891.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.-109+21196_-109+21 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTT | 6 | a0001c0001t0002g0039 a0001c0001t0002g0072 a0001c0002t0009g0205 others(3): Show |
6 | HG02145.hp1 HG03195.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+21195_-109+21 others(9): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTT | 77 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0109 others(74): Show |
77 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.-109+21194_-109+21 others(10): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTT | 31 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0117 others(28): Show |
31 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.-109+21193_-109+21 others(11): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTT | 9 | a0001c0001t0001g0103 a0001c0001t0001g0186 a0001c0001t0001g0187 others(6): Show |
9 | HG02074.hp2 HG02080.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+21192_-109+21 others(12): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0061 others(2): Show |
5 | HG02145.hp2 NA18940.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.-109+21188_-109+21 others(16): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-109+21187_-109+21 others(17): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0074 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-109+21185_-109+21 others(19): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(7): Show |
4 | a0001c0001t0002g0084 a0001c0001t0002g0170 a0001c0002t0003g0037 others(1): Show |
4 | HG01074.hp1 HG02818.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+21184_-109+21 others(20): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(8): Show |
3 | a0001c0001t0001g0016 a0001c0001t0007g0105 a0002c0003t0003g0080 |
3 | HG01069.hp1 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-109+21183_-109+21 others(21): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(9): Show |
4 | a0001c0002t0031g0214 a0002c0003t0003g0050 a0002c0003t0003g0051 others(1): Show |
4 | HG00423.hp1 HG02080.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+21182_-109+21 others(22): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(10): Show |
6 | a0001c0001t0001g0108 a0001c0001t0007g0085 a0001c0001t0007g0088 others(3): Show |
6 | HG01109.hp2 HG01496.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+21181_-109+21 others(23): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(11): Show |
4 | a0001c0001t0007g0044 a0001c0001t0007g0045 a0001c0001t0007g0087 others(1): Show |
4 | HG02809.hp2 HG04204.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+21180_-109+21 others(24): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0055 a0001c0001t0002g0095 a0001c0001t0007g0086 |
3 | HG00408.hp1 HG00642.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-109+21179_-109+21 others(25): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(13): Show |
4 | a0001c0002t0006g0032 a0001c0004t0013g0033 a0001c0004t0013g0195 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+21178_-109+21 others(26): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(14): Show |
2 | a0001c0001t0002g0198 a0001c0001t0002g0199 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-109+21177_-109+21 others(27): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(16): Show |
3 | a0001c0002t0006g0106 a0001c0007t0002g0040 a0002c0003t0003g0062 |
3 | HG02071.hp1 HG02451.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-109+21175_-109+21 others(29): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(17): Show |
2 | a0002c0003t0003g0063 a0002c0003t0003g0098 |
2 | HG00735.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-109+21197_-109+21 others(30): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(19): Show |
4 | a0001c0001t0002g0064 a0001c0001t0002g0076 a0001c0001t0002g0091 others(1): Show |
4 | HG01192.hp1 NA19056.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+21197_-109+21 others(32): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(20): Show |
2 | a0001c0001t0002g0065 a0002c0003t0003g0048 |
2 | HG00558.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-109+21197_-109+21 others(33): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(21): Show |
1 | a0002c0003t0003g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-109+21197_-109+21 others(34): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(22): Show |
2 | a0001c0001t0002g0046 a0001c0001t0002g0239 |
2 | HG00544.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.-109+21197_-109+21 others(35): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(23): Show |
5 | a0001c0001t0002g0024 a0001c0001t0002g0067 a0001c0001t0002g0200 others(2): Show |
5 | HG01192.hp2 HG02257.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+21197_-109+21 others(36): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(24): Show |
9 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0053 others(6): Show |
9 | HG01256.hp2 HG01261.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-109+21197_-109+21 others(37): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(25): Show |
2 | a0001c0001t0002g0069 a0001c0001t0002g0096 |
2 | HG02129.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-109+21197_-109+21 others(38): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(28): Show |
1 | a0002c0003t0003g0201 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-109+21197_-109+21 others(41): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(29): Show |
3 | a0001c0001t0002g0041 a0001c0001t0002g0078 a0001c0001t0002g0079 |
3 | HG00099.hp2 HG02083.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-109+21197_-109+21 others(42): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(30): Show |
3 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0002c0003t0003g0070 |
3 | HG02148.hp2 NA19081.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-109+21197_-109+21 others(43): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(33): Show |
1 | a0002c0003t0003g0099 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-109+21197_-109+21 others(46): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(34): Show |
1 | a0001c0001t0002g0071 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-109+21197_-109+21 others(47): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(35): Show |
1 | a0001c0001t0002g0097 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-109+21197_-109+21 others(48): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(36): Show |
1 | a0001c0001t0002g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-109+21197_-109+21 others(49): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | C | CTTTTTTT others(42): Show |
1 | a0002c0003t0003g0089 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-109+21197_-109+21 others(55): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | CTTTTTTT | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+21191_-109+21 others(13): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26578993 | CTTTTTTT others(1): Show |
C | 19 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-109+21190_-109+21 others(14): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26578993 | ||||||
| chr13:26579056 | A | G | 115 | a0001c0001t0001g0036 a0001c0001t0001g0108 a0001c0001t0002g0024 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.-109+21237A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26579056 | |||||||
| chr13:26579152 | A | G | 1 | a0001c0001t0005g0271 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-109+21333A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26579152 | |||||||
| chr13:26579161 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-109+21342A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26579161 | |||||||
| chr13:26579186 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-109+21367A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26579186 | |||||||
| chr13:26579190 | T | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
125 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-109+21371T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26579190 | |||||||
| chr13:26579350 | A | G | 115 | a0001c0001t0001g0036 a0001c0001t0001g0108 a0001c0001t0002g0024 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.-109+21531A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26579350 | |||||||
| chr13:26579657 | T | C | 19 | a0001c0001t0001g0125 a0001c0002t0004g0223 a0001c0002t0004g0224 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.-109+21838T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26579657 | |||||||
| chr13:26579672 | T | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-109+21853T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26579672 | |||||||
| chr13:26579798 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+21979A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26579798 | |||||||
| chr13:26579981 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+22162A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26579981 | |||||||
| chr13:26579987 | T | C | 1 | a0002c0003t0003g0062 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-109+22168T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26579987 | |||||||
| chr13:26580295 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-109+22476G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26580295 | |||||||
| chr13:26580298 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
125 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-109+22479G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26580298 | |||||||
| chr13:26580441 | A | G | 65 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(62): Show |
65 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-109+22622A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26580441 | |||||||
| chr13:26580464 | A | G | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+22645A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26580464 | |||||||
| chr13:26580626 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+22807C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26580626 | |||||||
| chr13:26580626 | CT | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(148): Show |
151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-109+22822delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26580626 | ||||||
| chr13:26580695 | G | A | 1 | a0001c0001t0005g0254 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-109+22876G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26580695 | |||||||
| chr13:26580711 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-109+22892C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26580711 | |||||||
| chr13:26580812 | A | G | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.-109+22993A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26580812 | |||||||
| chr13:26580833 | C | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(8): Show |
11 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-109+23014C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26580833 | |||||||
| chr13:26580873 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-109+23054G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26580873 | |||||||
| chr13:26580877 | G | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+23058G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26580877 | |||||||
| chr13:26580932 | C | CT | 122 | a0001c0001t0001g0036 a0001c0001t0001g0108 a0001c0001t0002g0024 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-109+23129dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26580932 | ||||||
| chr13:26580932 | C | CTT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(105): Show |
108 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-109+23128_-109+23 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26580932 | ||||||
| chr13:26580932 | C | CTTT | 6 | a0001c0001t0001g0113 a0001c0001t0001g0141 a0001c0001t0001g0145 others(3): Show |
6 | HG00544.hp1 HG01109.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+23127_-109+23 others(9): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26580932 | ||||||
| chr13:26580953 | C | T | 1 | a0001c0002t0004g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-109+23134C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26580953 | |||||||
| chr13:26581158 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-109+23339T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26581158 | |||||||
| chr13:26581222 | A | G | 6 | a0001c0001t0001g0036 a0001c0002t0011g0215 a0001c0004t0013g0033 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+23403A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26581222 | |||||||
| chr13:26581317 | T | A | 1 | a0001c0001t0020g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-109+23498T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26581317 | |||||||
| chr13:26581318 | T | A | 1 | a0001c0001t0020g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-109+23499T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26581318 | |||||||
| chr13:26581369 | G | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+23550G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26581369 | |||||||
| chr13:26581530 | A | G | 3 | a0002c0003t0011g0011 a0002c0003t0011g0012 a0002c0003t0011g0013 |
3 | HG02109.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-109+23711A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26581530 | |||||||
| chr13:26581847 | T | C | 1 | a0001c0001t0034g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-109+24028T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26581847 | |||||||
| chr13:26581920 | A | G | 22 | a0001c0001t0001g0112 a0001c0001t0001g0120 a0001c0001t0001g0121 others(19): Show |
22 | HG00423.hp2 HG00642.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.-109+24101A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26581920 | |||||||
| chr13:26581966 | T | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+24147T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26581966 | |||||||
| chr13:26582016 | C | G | 2 | a0001c0001t0005g0265 a0001c0001t0005g0267 |
2 | HG00639.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-109+24197C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26582016 | |||||||
| chr13:26582158 | T | G | 6 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0002g0285 others(3): Show |
6 | NA18612.hp2 NA18944.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+24339T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26582158 | |||||||
| chr13:26582170 | C | T | 19 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-109+24351C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26582170 | |||||||
| chr13:26582171 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-109+24352A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26582171 | |||||||
| chr13:26582303 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+24484A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26582303 | |||||||
| chr13:26582346 | T | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-109+24527T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26582346 | |||||||
| chr13:26582397 | C | T | 1 | a0001c0001t0014g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-109+24578C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26582397 | |||||||
| chr13:26582474 | G | A | 26 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(23): Show |
26 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.-109+24655G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26582474 | |||||||
| chr13:26582487 | G | T | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-109+24668G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26582487 | |||||||
| chr13:26582602 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-109+24783G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26582602 | |||||||
| chr13:26582617 | C | T | 1 | a0005c0006t0002g0057 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-109+24798C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26582617 | |||||||
| chr13:26582676 | C | CA | 101 | a0001c0001t0001g0108 a0001c0001t0001g0140 a0001c0001t0002g0024 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-109+24880dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26582676 | ||||||
| chr13:26582676 | C | CAA | 65 | a0001c0001t0001g0016 a0001c0001t0001g0102 a0001c0001t0001g0112 others(62): Show |
65 | HG00408.hp2 HG00423.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.-109+24879_-109+24 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26582676 | ||||||
| chr13:26582676 | C | CAAA | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
64 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-109+24878_-109+24 others(9): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26582676 | ||||||
| chr13:26582777 | G | A | 2 | a0001c0001t0010g0027 a0001c0001t0022g0168 |
2 | HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-109+24958G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26582777 | |||||||
| chr13:26582792 | C | T | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-109+24973C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26582792 | |||||||
| chr13:26583041 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-109+25222G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26583041 | |||||||
| chr13:26583059 | GGGTCTTA others(2): Show |
G | 6 | a0001c0001t0002g0272 a0001c0001t0002g0275 a0001c0001t0002g0277 others(3): Show |
6 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+25243_-109+25 others(15): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26583059 | ||||||
| chr13:26583126 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-109+25307A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26583126 | |||||||
| chr13:26583175 | G | T | 65 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(62): Show |
65 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-109+25356G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26583175 | |||||||
| chr13:26583321 | A | G | 1 | a0001c0001t0002g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-109+25502A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26583321 | |||||||
| chr13:26583566 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-109+25747C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26583566 | |||||||
| chr13:26583901 | G | C | 1 | a0001c0001t0001g0145 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-109+26082G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26583901 | |||||||
| chr13:26584205 | G | A | 2 | a0001c0002t0004g0223 a0001c0002t0004g0224 |
2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-109+26386G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26584205 | |||||||
| chr13:26584227 | G | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-109+26408G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26584227 | |||||||
| chr13:26584439 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(173): Show |
176 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.-109+26620T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26584439 | |||||||
| chr13:26584439 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-109+26620T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26584439 | |||||||
| chr13:26584677 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+26858A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26584677 | |||||||
| chr13:26585096 | T | TA | 115 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(112): Show |
115 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-109+27290dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26585096 | ||||||
| chr13:26585096 | T | TAA | 18 | a0001c0001t0005g0254 a0001c0001t0005g0255 a0001c0001t0005g0256 others(15): Show |
18 | HG00639.hp1 HG00735.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-109+27289_-109+27 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26585096 | ||||||
| chr13:26585267 | A | ATGTAAAC others(24): Show |
4 | a0001c0001t0005g0264 a0001c0001t0005g0268 a0001c0001t0005g0269 others(1): Show |
4 | HG01081.hp2 HG01169.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+27452_-109+27 others(37): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26585267 | ||||||
| chr13:26585734 | T | C | 1 | a0002c0003t0003g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-108-27227T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26585734 | |||||||
| chr13:26585784 | T | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-27177T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26585784 | |||||||
| chr13:26585793 | G | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-27168G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26585793 | |||||||
| chr13:26586046 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-26915A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26586046 | |||||||
| chr13:26586208 | G | A | 12 | a0001c0001t0008g0019 a0001c0002t0003g0152 a0001c0002t0009g0003 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.-108-26753G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26586208 | |||||||
| chr13:26586257 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-26704C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26586257 | |||||||
| chr13:26586449 | A | G | 5 | a0001c0002t0009g0003 a0001c0002t0009g0207 a0001c0002t0009g0212 others(2): Show |
5 | HG02055.hp1 HG03041.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-108-26512A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26586449 | |||||||
| chr13:26586684 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-26277T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26586684 | |||||||
| chr13:26586685 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-26276T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26586685 | |||||||
| chr13:26586698 | A | G | 3 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 |
3 | HG02717.hp2 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-108-26263A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26586698 | |||||||
| chr13:26586804 | G | A | 113 | a0001c0001t0001g0036 a0001c0001t0001g0108 a0001c0001t0002g0024 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-108-26157G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26586804 | |||||||
| chr13:26586823 | A | C | 1 | a0001c0001t0034g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-108-26138A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26586823 | |||||||
| chr13:26586917 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-108-26044C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26586917 | |||||||
| chr13:26586973 | C | T | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-25988C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26586973 | |||||||
| chr13:26586994 | T | C | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108-25967T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26586994 | |||||||
| chr13:26587082 | G | A | 3 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 |
3 | HG02717.hp2 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-108-25879G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26587082 | |||||||
| chr13:26587102 | C | CA | 80 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(77): Show |
80 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-108-25837dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26587102 | ||||||
| chr13:26587102 | C | CAA | 40 | a0001c0001t0001g0120 a0001c0001t0002g0047 a0001c0001t0002g0055 others(37): Show |
40 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-108-25838_-108-25 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26587102 | ||||||
| chr13:26587273 | G | GT | 18 | a0001c0001t0005g0254 a0001c0001t0005g0255 a0001c0001t0005g0256 others(15): Show |
18 | HG00639.hp1 HG00735.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-108-25676dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26587273 | ||||||
| chr13:26587273 | G | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-25688G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26587273 | |||||||
| chr13:26587629 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-108-25332C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26587629 | |||||||
| chr13:26587648 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-25313C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26587648 | |||||||
| chr13:26587661 | T | C | 3 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 |
3 | HG02622.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-108-25300T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26587661 | |||||||
| chr13:26587793 | G | A | 1 | a0001c0002t0003g0037 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-108-25168G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26587793 | |||||||
| chr13:26588069 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-24892T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26588069 | |||||||
| chr13:26588198 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0109 a0001c0001t0001g0111 others(44): Show |
47 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-108-24763G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26588198 | |||||||
| chr13:26588590 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
115 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-108-24371A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26588590 | |||||||
| chr13:26588620 | C | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(101): Show |
104 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-108-24341C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26588620 | |||||||
| chr13:26588626 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0137 a0001c0001t0001g0141 |
3 | HG01928.hp2 HG01934.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-108-24335G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26588626 | |||||||
| chr13:26588630 | G | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(167): Show |
170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-108-24331G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26588630 | |||||||
| chr13:26588937 | A | G | 1 | a0001c0001t0014g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-108-24024A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26588937 | |||||||
| chr13:26588963 | A | G | 12 | a0001c0001t0008g0019 a0001c0002t0003g0152 a0001c0002t0009g0003 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.-108-23998A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26588963 | |||||||
| chr13:26589014 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-23947A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26589014 | |||||||
| chr13:26589083 | T | C | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108-23878T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26589083 | |||||||
| chr13:26589202 | A | G | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-23759A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26589202 | |||||||
| chr13:26589437 | G | A | 1 | a0001c0001t0014g0143 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-108-23524G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26589437 | |||||||
| chr13:26589564 | T | C | 1 | a0001c0001t0007g0086 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-108-23397T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26589564 | |||||||
| chr13:26589660 | A | T | 1 | a0001c0002t0025g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-108-23301A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26589660 | |||||||
| chr13:26589696 | G | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-23265G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26589696 | |||||||
| chr13:26589920 | T | TA | 7 | a0001c0002t0009g0003 a0001c0002t0009g0207 a0001c0002t0009g0209 others(4): Show |
7 | HG02055.hp1 HG03041.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-108-23040dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26589920 | ||||||
| chr13:26590196 | T | A | 13 | a0001c0001t0002g0281 a0001c0001t0008g0019 a0001c0002t0003g0152 others(10): Show |
13 | HG01515.hp2 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-108-22765T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26590196 | |||||||
| chr13:26590228 | G | GC | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-22726dupC | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26590228 | ||||||
| chr13:26590371 | A | G | 4 | a0001c0001t0005g0264 a0001c0001t0005g0268 a0001c0001t0005g0269 others(1): Show |
4 | HG01081.hp2 HG01169.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-22590A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26590371 | |||||||
| chr13:26590547 | TG | T | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108-22411delG | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26590547 | ||||||
| chr13:26590649 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-108-22312A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26590649 | |||||||
| chr13:26590711 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-108-22250T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26590711 | |||||||
| chr13:26590760 | A | T | 64 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(61): Show |
64 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-108-22201A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26590760 | |||||||
| chr13:26590860 | A | G | 1 | a0001c0004t0024g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-108-22101A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26590860 | |||||||
| chr13:26590930 | A | G | 19 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-22031A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26590930 | |||||||
| chr13:26591286 | T | G | 1 | a0001c0004t0013g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-108-21675T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26591286 | |||||||
| chr13:26591439 | G | A | 1 | a0001c0002t0009g0003 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-108-21522G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26591439 | |||||||
| chr13:26591562 | G | A | 1 | a0001c0001t0005g0264 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-108-21399G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26591562 | |||||||
| chr13:26591562 | G | C | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-108-21399G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26591562 | |||||||
| chr13:26591596 | G | A | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-21365G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26591596 | |||||||
| chr13:26591611 | T | C | 1 | a0001c0002t0019g0217 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-108-21350T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26591611 | |||||||
| chr13:26591889 | C | T | 1 | a0001c0004t0024g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-108-21072C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26591889 | |||||||
| chr13:26592026 | GT | G | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
51 | HG00408.hp1 HG00639.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.-108-20916delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26592026 | ||||||
| chr13:26592026 | GTT | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0102 others(190): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.-108-20917_-108-20 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26592026 | ||||||
| chr13:26592055 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-108-20906C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592055 | |||||||
| chr13:26592089 | AT | A | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-20869delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26592089 | ||||||
| chr13:26592159 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-108-20802G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592159 | |||||||
| chr13:26592198 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(103): Show |
106 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-108-20763A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592198 | |||||||
| chr13:26592225 | T | A | 1 | a0001c0001t0001g0131 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-108-20736T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592225 | |||||||
| chr13:26592362 | G | A | 3 | a0001c0001t0002g0053 a0001c0001t0002g0067 a0001c0001t0002g0077 |
3 | NA18952.hp2 NA18969.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-108-20599G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592362 | |||||||
| chr13:26592373 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-108-20588G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592373 | |||||||
| chr13:26592526 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-108-20435A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592526 | |||||||
| chr13:26592530 | C | T | 1 | a0001c0001t0002g0284 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-108-20431C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592530 | |||||||
| chr13:26592568 | GTC | G | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-20389_-108-20 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26592568 | ||||||
| chr13:26592593 | C | T | 1 | a0001c0002t0006g0030 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-108-20368C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592593 | |||||||
| chr13:26592602 | C | G | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-20359C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592602 | |||||||
| chr13:26592613 | C | A | 19 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-20348C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592613 | |||||||
| chr13:26592846 | G | A | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-20115G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592846 | |||||||
| chr13:26592913 | C | A | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-20048C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592913 | |||||||
| chr13:26592949 | G | A | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0032g0101 others(2): Show |
5 | HG02083.hp2 NA19001.hp2 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108-20012G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26592949 | |||||||
| chr13:26593041 | G | A | 3 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 |
3 | HG02717.hp2 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-108-19920G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593041 | |||||||
| chr13:26593068 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-108-19893G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593068 | |||||||
| chr13:26593193 | G | A | 6 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0002g0285 others(3): Show |
6 | NA18612.hp2 NA18944.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-19768G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593193 | |||||||
| chr13:26593221 | TTTAGC | T | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-19739_-108-19 others(11): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593221 | |||||||
| chr13:26593265 | C | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-108-19696C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593265 | |||||||
| chr13:26593390 | G | A | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-19571G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593390 | |||||||
| chr13:26593427 | A | G | 3 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 |
3 | HG02622.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-108-19534A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593427 | |||||||
| chr13:26593476 | A | G | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-19485A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593476 | |||||||
| chr13:26593541 | T | C | 2 | a0001c0001t0010g0027 a0001c0001t0022g0168 |
2 | HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-108-19420T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593541 | |||||||
| chr13:26593562 | T | C | 1 | a0001c0002t0035g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-108-19399T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593562 | |||||||
| chr13:26593566 | T | A | 2 | a0001c0001t0010g0220 a0001c0001t0010g0221 |
2 | HG02602.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-108-19395T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593566 | |||||||
| chr13:26593589 | A | G | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-19372A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593589 | |||||||
| chr13:26593704 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
114 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-108-19257A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593704 | |||||||
| chr13:26593913 | G | T | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-19048G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593913 | |||||||
| chr13:26593967 | G | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-18994G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26593967 | |||||||
| chr13:26594005 | A | G | 7 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0131 others(4): Show |
7 | HG02056.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.-108-18956A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26594005 | |||||||
| chr13:26594085 | A | T | 73 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(70): Show |
73 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-108-18876A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26594085 | |||||||
| chr13:26594187 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-108-18774A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26594187 | |||||||
| chr13:26594455 | C | T | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-18506C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26594455 | |||||||
| chr13:26594517 | G | C | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-108-18444G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26594517 | |||||||
| chr13:26594606 | A | T | 1 | a0001c0004t0013g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-108-18355A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26594606 | |||||||
| chr13:26594680 | A | G | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-18281A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26594680 | |||||||
| chr13:26594729 | G | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0179 |
2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-108-18232G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26594729 | |||||||
| chr13:26594745 | C | G | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-18216C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26594745 | |||||||
| chr13:26594824 | AT | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-108-18135delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26594824 | ||||||
| chr13:26594905 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-108-18056G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26594905 | |||||||
| chr13:26595054 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-108-17907G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26595054 | |||||||
| chr13:26595169 | A | G | 1 | a0001c0001t0005g0256 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-108-17792A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26595169 | |||||||
| chr13:26595350 | T | G | 1 | a0001c0002t0028g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-108-17611T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26595350 | |||||||
| chr13:26595489 | C | T | 1 | a0001c0001t0002g0281 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-108-17472C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26595489 | |||||||
| chr13:26595581 | G | T | 73 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(70): Show |
73 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-108-17380G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26595581 | |||||||
| chr13:26595588 | C | T | 2 | a0001c0001t0002g0281 a0001c0001t0012g0194 |
2 | HG01168.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-108-17373C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26595588 | |||||||
| chr13:26595654 | A | G | 27 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(24): Show |
27 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.-108-17307A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26595654 | |||||||
| chr13:26595725 | G | A | 1 | a0001c0002t0004g0231 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-108-17236G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26595725 | |||||||
| chr13:26595778 | A | G | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-17183A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26595778 | |||||||
| chr13:26596112 | CT | C | 60 | a0001c0001t0001g0108 a0001c0001t0001g0127 a0001c0001t0002g0002 others(57): Show |
61 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.-108-16831delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26596112 | ||||||
| chr13:26596112 | CTT | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-108-16832_-108-16 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26596112 | ||||||
| chr13:26596264 | T | A | 3 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 |
3 | HG01109.hp2 HG02145.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-108-16697T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26596264 | |||||||
| chr13:26596297 | A | AT | 10 | a0001c0001t0001g0108 a0001c0001t0002g0090 a0001c0001t0007g0044 others(7): Show |
10 | HG00673.hp2 HG01496.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-16654dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26596297 | ||||||
| chr13:26596312 | T | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-108-16649T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26596312 | |||||||
| chr13:26596342 | T | A | 10 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(7): Show |
10 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-16619T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26596342 | |||||||
| chr13:26596343 | T | A | 27 | a0001c0001t0001g0036 a0001c0001t0001g0108 a0001c0001t0001g0129 others(24): Show |
27 | HG00738.hp2 HG01496.hp1 HG02074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-108-16618T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26596343 | |||||||
| chr13:26596477 | G | T | 1 | a0001c0001t0002g0274 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-108-16484G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26596477 | |||||||
| chr13:26596579 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
113 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-108-16382G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26596579 | |||||||
| chr13:26596655 | C | T | 9 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0006g0030 others(6): Show |
9 | HG01074.hp1 HG01192.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-16306C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26596655 | |||||||
| chr13:26596889 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-108-16072G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26596889 | |||||||
| chr13:26596921 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0109 a0001c0001t0001g0111 others(44): Show |
47 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-108-16040C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26596921 | |||||||
| chr13:26596923 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-108-16038G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26596923 | |||||||
| chr13:26596935 | T | A | 1 | a0001c0001t0001g0174 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-108-16026T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26596935 | |||||||
| chr13:26597193 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(234): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-108-15768T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26597193 | |||||||
| chr13:26597196 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-108-15765A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26597196 | |||||||
| chr13:26597414 | C | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0169 |
3 | HG01891.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-108-15547C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26597414 | |||||||
| chr13:26597423 | C | T | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-108-15538C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26597423 | |||||||
| chr13:26597444 | T | TTTG | 6 | a0001c0002t0003g0152 a0001c0002t0006g0030 a0001c0002t0006g0031 others(3): Show |
6 | HG02148.hp1 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-15493_-108-15 others(9): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26597444 | ||||||
| chr13:26597447 | G | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0218 a0001c0002t0009g0212 |
3 | HG01099.hp2 HG03225.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-108-15514G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26597447 | |||||||
| chr13:26597475 | C | T | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-15486C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26597475 | |||||||
| chr13:26597484 | C | CT | 12 | a0001c0001t0001g0109 a0001c0001t0001g0160 a0001c0002t0009g0003 others(9): Show |
12 | HG01943.hp1 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-108-15467dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26597484 | ||||||
| chr13:26597529 | C | T | 1 | a0001c0001t0012g0192 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-108-15432C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26597529 | |||||||
| chr13:26597633 | A | G | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-15328A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26597633 | |||||||
| chr13:26597663 | T | G | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-15298T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26597663 | |||||||
| chr13:26597707 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-108-15254C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26597707 | |||||||
| chr13:26597971 | G | A | 1 | a0001c0002t0004g0228 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-108-14990G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26597971 | |||||||
| chr13:26598056 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.-108-14905A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26598056 | |||||||
| chr13:26598138 | T | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-108-14823T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26598138 | |||||||
| chr13:26598198 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-108-14763G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26598198 | |||||||
| chr13:26598451 | G | A | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-108-14510G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26598451 | |||||||
| chr13:26598609 | C | T | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-14352C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26598609 | |||||||
| chr13:26598649 | C | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-108-14312C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26598649 | |||||||
| chr13:26598661 | C | T | 1 | a0001c0002t0003g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-108-14300C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26598661 | |||||||
| chr13:26598676 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-14285C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26598676 | |||||||
| chr13:26598685 | G | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-14276G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26598685 | |||||||
| chr13:26598705 | T | C | 1 | a0002c0003t0003g0062 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-108-14256T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26598705 | |||||||
| chr13:26598819 | G | T | 1 | a0001c0001t0002g0287 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-108-14142G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26598819 | |||||||
| chr13:26598966 | G | A | 27 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(24): Show |
27 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.-108-13995G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26598966 | |||||||
| chr13:26599014 | A | G | 1 | a0001c0001t0002g0275 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-108-13947A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26599014 | |||||||
| chr13:26599046 | T | C | 2 | a0001c0001t0001g0036 a0001c0004t0024g0196 |
2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-108-13915T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26599046 | |||||||
| chr13:26599184 | C | CTT | 7 | a0001c0001t0001g0036 a0001c0002t0004g0223 a0001c0002t0004g0224 others(4): Show |
7 | HG01069.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-108-13761_-108-13 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26599184 | ||||||
| chr13:26599184 | C | CTTT | 87 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-108-13762_-108-13 others(9): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26599184 | ||||||
| chr13:26599184 | C | CTTTT | 115 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(112): Show |
115 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-108-13763_-108-13 others(10): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26599184 | ||||||
| chr13:26599184 | C | CTTTTT | 9 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
9 | HG00639.hp2 HG01934.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-13764_-108-13 others(11): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26599184 | ||||||
| chr13:26599207 | G | A | 4 | a0001c0002t0009g0205 a0001c0002t0009g0208 a0001c0002t0009g0209 others(1): Show |
4 | HG02145.hp1 HG03195.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-13754G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26599207 | |||||||
| chr13:26599348 | A | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(106): Show |
109 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-108-13613A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26599348 | |||||||
| chr13:26599427 | G | A | 1 | a0001c0004t0024g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-108-13534G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26599427 | |||||||
| chr13:26599460 | G | A | 1 | a0001c0001t0005g0266 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-108-13501G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26599460 | |||||||
| chr13:26599676 | A | G | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-13285A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26599676 | |||||||
| chr13:26599762 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-108-13199C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26599762 | |||||||
| chr13:26599845 | G | A | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-13116G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26599845 | |||||||
| chr13:26600065 | G | A | 27 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(24): Show |
27 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.-108-12896G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26600065 | |||||||
| chr13:26600290 | T | A | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-12671T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26600290 | |||||||
| chr13:26600375 | G | A | 18 | a0001c0001t0005g0254 a0001c0001t0005g0255 a0001c0001t0005g0256 others(15): Show |
18 | HG00639.hp1 HG00735.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-108-12586G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26600375 | |||||||
| chr13:26600417 | A | G | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-108-12544A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26600417 | |||||||
| chr13:26600504 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-108-12457A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26600504 | |||||||
| chr13:26600586 | A | T | 1 | a0001c0002t0003g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-108-12375A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26600586 | |||||||
| chr13:26600649 | G | A | 1 | a0001c0001t0010g0162 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-108-12312G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26600649 | |||||||
| chr13:26600814 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-108-12147A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26600814 | |||||||
| chr13:26600815 | T | A | 4 | a0001c0002t0006g0213 a0002c0003t0011g0011 a0002c0003t0011g0012 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-12146T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26600815 | |||||||
| chr13:26601054 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-108-11907C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26601054 | |||||||
| chr13:26601404 | C | CA | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-108-11555dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26601404 | ||||||
| chr13:26601457 | A | G | 1 | a0001c0002t0004g0225 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-108-11504A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26601457 | |||||||
| chr13:26601644 | A | G | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-11317A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26601644 | |||||||
| chr13:26601996 | G | A | 1 | a0001c0002t0006g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-108-10965G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26601996 | |||||||
| chr13:26602156 | G | A | 1 | a0001c0001t0005g0271 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-108-10805G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26602156 | |||||||
| chr13:26602226 | T | C | 1 | a0001c0004t0013g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-108-10735T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26602226 | |||||||
| chr13:26602553 | T | G | 1 | a0001c0002t0004g0223 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-108-10408T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26602553 | |||||||
| chr13:26602851 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-108-10110A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26602851 | |||||||
| chr13:26603050 | G | A | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-9911G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26603050 | |||||||
| chr13:26603079 | C | T | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-108-9882C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26603079 | |||||||
| chr13:26603128 | G | A | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-9833G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26603128 | |||||||
| chr13:26603289 | T | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.-108-9672T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26603289 | |||||||
| chr13:26603348 | G | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-9613G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26603348 | |||||||
| chr13:26603434 | G | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-9527G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26603434 | |||||||
| chr13:26603726 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-108-9235G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26603726 | |||||||
| chr13:26603790 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-108-9171A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26603790 | |||||||
| chr13:26603862 | TAAAC | T | 3 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 |
3 | HG02717.hp2 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-108-9097_-108-909 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26603862 | ||||||
| chr13:26604031 | A | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-108-8930A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26604031 | |||||||
| chr13:26604142 | A | AT | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-8811dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26604142 | ||||||
| chr13:26604143 | T | A | 9 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0006g0030 others(6): Show |
9 | HG01074.hp1 HG01192.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-8818T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26604143 | |||||||
| chr13:26604170 | C | T | 15 | a0001c0001t0002g0002 a0001c0001t0002g0273 a0001c0001t0002g0274 others(12): Show |
16 | HG00741.hp2 HG01261.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.-108-8791C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26604170 | |||||||
| chr13:26604416 | TA | T | 7 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0002t0004g0021 others(4): Show |
7 | HG01175.hp1 HG01175.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-108-8544delA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26604416 | |||||||
| chr13:26604706 | T | C | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108-8255T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26604706 | |||||||
| chr13:26604812 | C | T | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-8149C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26604812 | |||||||
| chr13:26605076 | C | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0119 a0001c0001t0001g0127 others(13): Show |
16 | HG00558.hp1 HG02027.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-108-7885C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605076 | |||||||
| chr13:26605082 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-108-7879C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605082 | |||||||
| chr13:26605096 | C | T | 1 | a0001c0002t0004g0236 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-108-7865C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605096 | |||||||
| chr13:26605129 | T | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-108-7832T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605129 | |||||||
| chr13:26605149 | A | G | 1 | a0001c0001t0002g0286 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-108-7812A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605149 | |||||||
| chr13:26605433 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-108-7528C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605433 | |||||||
| chr13:26605482 | T | G | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-7479T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605482 | |||||||
| chr13:26605485 | G | C | 2 | a0001c0002t0016g0010 a0001c0002t0016g0014 |
2 | HG00738.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-108-7476G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605485 | |||||||
| chr13:26605550 | A | G | 1 | a0001c0002t0004g0225 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-108-7411A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605550 | |||||||
| chr13:26605622 | T | C | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-7339T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605622 | |||||||
| chr13:26605732 | C | A | 1 | a0001c0001t0002g0278 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-108-7229C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605732 | |||||||
| chr13:26605754 | T | G | 4 | a0001c0002t0006g0213 a0002c0003t0011g0011 a0002c0003t0011g0012 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-7207T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605754 | |||||||
| chr13:26605956 | G | A | 1 | a0001c0001t0007g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-108-7005G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605956 | |||||||
| chr13:26605965 | G | A | 1 | a0001c0002t0035g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-108-6996G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26605965 | |||||||
| chr13:26606136 | G | T | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-6825G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26606136 | |||||||
| chr13:26606222 | A | C | 1 | a0001c0001t0005g0255 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-108-6739A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26606222 | |||||||
| chr13:26606308 | TTC | T | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-6649_-108-664 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26606308 | ||||||
| chr13:26606321 | C | CGT | 9 | a0001c0001t0002g0002 a0001c0001t0002g0281 a0001c0001t0002g0291 others(6): Show |
10 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-6597_-108-659 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26606321 | ||||||
| chr13:26606321 | C | CGTGT | 12 | a0001c0001t0002g0273 a0001c0001t0002g0276 a0001c0001t0002g0282 others(9): Show |
12 | HG00735.hp2 HG01243.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.-108-6599_-108-659 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26606321 | ||||||
| chr13:26606321 | C | CGTGTGT | 10 | a0001c0001t0002g0253 a0001c0001t0002g0287 a0001c0001t0002g0290 others(7): Show |
10 | HG01081.hp2 HG01255.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-108-6601_-108-659 others(10): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26606321 | ||||||
| chr13:26606321 | C | CGTGTGTG others(1): Show |
7 | a0001c0001t0002g0275 a0001c0001t0002g0283 a0001c0001t0002g0285 others(4): Show |
7 | HG01169.hp2 HG01433.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-108-6603_-108-659 others(12): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26606321 | ||||||
| chr13:26606321 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0002g0274 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-108-6605_-108-659 others(14): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26606321 | ||||||
| chr13:26606321 | CGT | C | 26 | a0001c0001t0002g0028 a0001c0001t0002g0042 a0001c0001t0002g0068 others(23): Show |
26 | HG01069.hp1 HG01168.hp2 HG02148.hp1 others(23): Show |
intron_variant | MODIFIER | c.-108-6597_-108-659 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26606321 | ||||||
| chr13:26606321 | CGTGT | C | 56 | a0001c0001t0001g0016 a0001c0001t0002g0024 a0001c0001t0002g0029 others(53): Show |
56 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-108-6599_-108-659 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26606321 | ||||||
| chr13:26606321 | CGTGTGT | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(24): Show |
27 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-108-6601_-108-659 others(10): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26606321 | ||||||
| chr13:26606321 | CGTGTGTG others(1): Show |
C | 28 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0140 others(25): Show |
28 | HG00099.hp1 HG00544.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-108-6603_-108-659 others(12): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26606321 | ||||||
| chr13:26606321 | CGTGTGTG others(3): Show |
C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(91): Show |
94 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.-108-6605_-108-659 others(14): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26606321 | ||||||
| chr13:26606321 | CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0001g0184 a0001c0002t0031g0214 |
2 | HG01109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-108-6607_-108-659 others(16): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26606321 | ||||||
| chr13:26606458 | C | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-108-6503C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26606458 | |||||||
| chr13:26606522 | A | AT | 7 | a0001c0001t0007g0045 a0001c0001t0023g0094 a0001c0002t0009g0209 others(4): Show |
7 | HG02074.hp1 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-108-6422dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26606522 | ||||||
| chr13:26606565 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-6396C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26606565 | |||||||
| chr13:26606625 | G | A | 1 | a0001c0001t0002g0281 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-108-6336G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26606625 | |||||||
| chr13:26606810 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-108-6151G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26606810 | |||||||
| chr13:26606839 | C | G | 6 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0002g0285 others(3): Show |
6 | NA18612.hp2 NA18944.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-6122C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26606839 | |||||||
| chr13:26607080 | G | A | 1 | a0001c0002t0011g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-108-5881G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26607080 | |||||||
| chr13:26607090 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-108-5871T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26607090 | |||||||
| chr13:26607122 | G | A | 7 | a0001c0002t0006g0213 a0001c0002t0011g0215 a0001c0002t0011g0216 others(4): Show |
7 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-108-5839G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26607122 | |||||||
| chr13:26607125 | T | A | 2 | a0001c0001t0002g0079 a0001c0001t0002g0090 |
2 | HG00673.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-108-5836T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26607125 | |||||||
| chr13:26607226 | T | C | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-108-5735T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26607226 | |||||||
| chr13:26607271 | A | G | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-5690A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26607271 | |||||||
| chr13:26607384 | G | A | 1 | a0001c0002t0006g0107 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-108-5577G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26607384 | |||||||
| chr13:26607523 | C | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-5438C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26607523 | |||||||
| chr13:26607577 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-108-5384T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26607577 | |||||||
| chr13:26607639 | G | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0142 |
2 | HG01123.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-108-5322G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26607639 | |||||||
| chr13:26607864 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-5097A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26607864 | |||||||
| chr13:26607880 | C | T | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-108-5081C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26607880 | |||||||
| chr13:26607885 | C | G | 116 | a0001c0001t0001g0036 a0001c0001t0001g0218 a0001c0001t0002g0024 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-108-5076C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26607885 | |||||||
| chr13:26607999 | G | GCCTA | 44 | a0001c0001t0001g0108 a0001c0001t0002g0002 a0001c0001t0002g0253 others(41): Show |
45 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.-108-4961_-108-495 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26607999 | ||||||
| chr13:26608041 | A | AC | 19 | a0001c0001t0001g0111 a0001c0001t0001g0135 a0001c0001t0001g0181 others(16): Show |
19 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-4913dupC | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26608041 | ||||||
| chr13:26608094 | T | G | 1 | a0001c0002t0003g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-108-4867T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26608094 | |||||||
| chr13:26608102 | G | A | 21 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 others(18): Show |
21 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-108-4859G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26608102 | |||||||
| chr13:26608121 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0163 |
2 | HG02071.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-108-4840G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26608121 | |||||||
| chr13:26608226 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-108-4735G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26608226 | |||||||
| chr13:26608463 | T | G | 1 | a0001c0001t0029g0157 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-108-4498T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26608463 | |||||||
| chr13:26608494 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-4467A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26608494 | |||||||
| chr13:26608675 | C | T | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-4286C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26608675 | |||||||
| chr13:26608713 | G | A | 64 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(61): Show |
64 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-108-4248G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26608713 | |||||||
| chr13:26608837 | G | A | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-4124G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26608837 | |||||||
| chr13:26609290 | G | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-108-3671G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26609290 | |||||||
| chr13:26609361 | A | T | 1 | a0001c0001t0005g0256 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-108-3600A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26609361 | |||||||
| chr13:26609402 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-108-3559C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26609402 | |||||||
| chr13:26609475 | C | CT | 16 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(13): Show |
16 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-108-3469dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26609475 | ||||||
| chr13:26609475 | CT | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.-108-3469delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26609475 | ||||||
| chr13:26609558 | A | G | 1 | a0001c0001t0002g0274 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-108-3403A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26609558 | |||||||
| chr13:26609646 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-108-3315T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26609646 | |||||||
| chr13:26609824 | A | G | 2 | a0001c0002t0003g0037 a0001c0002t0003g0038 |
2 | HG01074.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-108-3137A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26609824 | |||||||
| chr13:26609842 | T | G | 1 | a0001c0001t0005g0271 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-108-3119T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26609842 | |||||||
| chr13:26609864 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-3097A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26609864 | |||||||
| chr13:26609917 | C | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0179 |
2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-108-3044C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26609917 | |||||||
| chr13:26609946 | T | G | 3 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 |
3 | HG01109.hp2 HG02145.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-108-3015T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26609946 | |||||||
| chr13:26609956 | A | T | 3 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 |
3 | HG01109.hp2 HG02145.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-108-3005A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26609956 | |||||||
| chr13:26610037 | T | G | 6 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-2924T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610037 | |||||||
| chr13:26610047 | G | A | 76 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(73): Show |
76 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.-108-2914G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610047 | |||||||
| chr13:26610138 | G | A | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-2823G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610138 | |||||||
| chr13:26610146 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-108-2815A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610146 | |||||||
| chr13:26610273 | C | T | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-108-2688C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610273 | |||||||
| chr13:26610373 | C | T | 10 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(7): Show |
10 | HG01496.hp1 HG02080.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-2588C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610373 | |||||||
| chr13:26610481 | C | G | 1 | a0001c0001t0021g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-108-2480C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610481 | |||||||
| chr13:26610500 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-2461A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610500 | |||||||
| chr13:26610546 | A | G | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-2415A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610546 | |||||||
| chr13:26610590 | A | G | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-2371A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610590 | |||||||
| chr13:26610680 | A | G | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-2281A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610680 | |||||||
| chr13:26610735 | T | C | 64 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(61): Show |
64 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-108-2226T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610735 | |||||||
| chr13:26610797 | C | T | 1 | a0001c0004t0024g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-108-2164C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610797 | |||||||
| chr13:26610847 | A | G | 40 | a0001c0001t0002g0002 a0001c0001t0002g0253 a0001c0001t0002g0272 others(37): Show |
41 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-108-2114A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610847 | |||||||
| chr13:26610969 | G | T | 19 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-1992G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610969 | |||||||
| chr13:26610976 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-108-1985G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26610976 | |||||||
| chr13:26611031 | C | CT | 65 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(62): Show |
66 | HG00544.hp2 HG00558.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.-108-1910dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26611031 | ||||||
| chr13:26611031 | C | CTT | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(109): Show |
112 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-108-1911_-108-191 others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26611031 | ||||||
| chr13:26611031 | C | CTTT | 12 | a0001c0001t0001g0036 a0001c0001t0001g0120 a0001c0001t0001g0139 others(9): Show |
12 | HG01109.hp1 HG01515.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.-108-1912_-108-191 others(7): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26611031 | ||||||
| chr13:26611031 | C | CTTTT | 19 | a0001c0001t0001g0189 a0001c0002t0004g0223 a0001c0002t0004g0224 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-1913_-108-191 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26611031 | ||||||
| chr13:26611052 | G | T | 1 | a0001c0004t0024g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-108-1909G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26611052 | |||||||
| chr13:26611196 | T | G | 1 | a0001c0002t0006g0031 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-108-1765T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26611196 | |||||||
| chr13:26611329 | A | G | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-108-1632A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26611329 | |||||||
| chr13:26611447 | C | T | 7 | a0001c0002t0004g0233 a0001c0002t0011g0215 a0001c0002t0011g0216 others(4): Show |
7 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-108-1514C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26611447 | |||||||
| chr13:26611478 | A | G | 1 | a0001c0002t0004g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-108-1483A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26611478 | |||||||
| chr13:26611517 | A | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.-108-1444A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26611517 | |||||||
| chr13:26611559 | G | A | 2 | a0001c0002t0003g0037 a0001c0002t0003g0038 |
2 | HG01074.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-108-1402G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26611559 | |||||||
| chr13:26611637 | A | G | 1 | a0002c0003t0003g0062 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-108-1324A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26611637 | |||||||
| chr13:26611711 | T | C | 1 | a0001c0001t0002g0281 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-108-1250T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26611711 | |||||||
| chr13:26611755 | G | C | 1 | a0001c0001t0015g0015 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-108-1206G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26611755 | |||||||
| chr13:26611801 | A | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-108-1160A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26611801 | |||||||
| chr13:26611836 | A | AT | 103 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(100): Show |
103 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-108-1113dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 26611836 | ||||||
| chr13:26611923 | G | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-1038G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26611923 | |||||||
| chr13:26612068 | G | C | 1 | a0001c0001t0001g0189 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-108-893G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26612068 | |||||||
| chr13:26612070 | C | G | 1 | a0001c0001t0001g0189 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-108-891C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26612070 | |||||||
| chr13:26612075 | T | A | 19 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-886T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26612075 | |||||||
| chr13:26612105 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.-108-856G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26612105 | |||||||
| chr13:26612283 | C | G | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-678C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26612283 | |||||||
| chr13:26612371 | A | T | 1 | a0001c0002t0019g0217 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-108-590A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26612371 | |||||||
| chr13:26612706 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
112 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-108-255T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26612706 | |||||||
| chr13:26612750 | A | G | 21 | a0001c0001t0002g0002 a0001c0001t0002g0272 a0001c0001t0002g0273 others(18): Show |
22 | HG00741.hp2 HG01261.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.-108-211A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 1/9 | chr13 | 26612750 | |||||||
| chr13:26613235 | T | A | 2 | a0001c0002t0004g0223 a0001c0002t0004g0224 |
2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-11+177T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26613235 | |||||||
| chr13:26613299 | A | G | 1 | a0001c0001t0020g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-11+241A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26613299 | |||||||
| chr13:26613433 | C | G | 1 | a0001c0001t0002g0078 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-11+375C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26613433 | |||||||
| chr13:26613491 | C | T | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+433C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26613491 | |||||||
| chr13:26613637 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-11+579G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26613637 | |||||||
| chr13:26613709 | G | A | 1 | a0001c0001t0010g0162 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-11+651G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26613709 | |||||||
| chr13:26613894 | C | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-11+836C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26613894 | |||||||
| chr13:26613997 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-11+939A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26613997 | |||||||
| chr13:26614065 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-11+1007C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26614065 | |||||||
| chr13:26614144 | G | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-11+1086G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26614144 | |||||||
| chr13:26614325 | A | C | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+1267A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26614325 | |||||||
| chr13:26614426 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-11+1368G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26614426 | |||||||
| chr13:26614640 | A | G | 76 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(73): Show |
76 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.-11+1582A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26614640 | |||||||
| chr13:26614859 | A | G | 2 | a0001c0002t0009g0207 a0001c0002t0009g0212 |
2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-11+1801A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26614859 | |||||||
| chr13:26614876 | C | T | 4 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+1818C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26614876 | |||||||
| chr13:26614952 | CTGT | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-11+1901_-11+1903d others(5): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26614952 | ||||||
| chr13:26615089 | T | A | 1 | a0001c0001t0002g0084 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-11+2031T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26615089 | |||||||
| chr13:26615288 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-11+2230T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26615288 | |||||||
| chr13:26615412 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0010g0001 |
2 | NA18982.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-11+2354G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26615412 | |||||||
| chr13:26615445 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0109 a0001c0001t0001g0111 others(44): Show |
47 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-11+2387G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26615445 | |||||||
| chr13:26615529 | G | A | 3 | a0001c0002t0018g0020 a0001c0002t0018g0023 a0004c0008t0036g0018 |
3 | HG01175.hp1 HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-11+2471G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26615529 | |||||||
| chr13:26615746 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(104): Show |
107 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-11+2688G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26615746 | |||||||
| chr13:26615973 | A | G | 2 | a0001c0002t0003g0037 a0001c0002t0003g0038 |
2 | HG01074.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-11+2915A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26615973 | |||||||
| chr13:26615996 | AGTTT | A | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11+2945_-11+2948d others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26615996 | ||||||
| chr13:26616000 | T | G | 1 | a0001c0001t0002g0290 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-11+2942T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26616000 | |||||||
| chr13:26616103 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-11+3045C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26616103 | |||||||
| chr13:26616464 | A | G | 1 | a0001c0002t0011g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+3406A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26616464 | |||||||
| chr13:26616760 | T | A | 1 | a0001c0001t0001g0121 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-11+3702T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26616760 | |||||||
| chr13:26616930 | A | G | 1 | a0001c0002t0004g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-11+3872A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26616930 | |||||||
| chr13:26617054 | T | C | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11+3996T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26617054 | |||||||
| chr13:26617142 | A | T | 1 | a0001c0002t0004g0240 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-11+4084A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26617142 | |||||||
| chr13:26617265 | G | GT | 6 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+4217dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26617265 | ||||||
| chr13:26617265 | G | T | 7 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0131 others(4): Show |
7 | HG02056.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+4207G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26617265 | |||||||
| chr13:26617265 | GT | G | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11+4217delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26617265 | ||||||
| chr13:26617719 | A | G | 40 | a0001c0001t0002g0002 a0001c0001t0002g0253 a0001c0001t0002g0272 others(37): Show |
41 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-11+4661A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26617719 | |||||||
| chr13:26617840 | C | T | 3 | a0002c0003t0011g0011 a0002c0003t0011g0012 a0002c0003t0011g0013 |
3 | HG02109.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-11+4782C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26617840 | |||||||
| chr13:26617860 | G | C | 2 | a0001c0002t0017g0229 a0001c0002t0017g0232 |
2 | HG01081.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-11+4802G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26617860 | |||||||
| chr13:26618022 | C | G | 4 | a0001c0001t0002g0046 a0001c0001t0002g0198 a0001c0001t0002g0199 others(1): Show |
4 | HG01070.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+4964C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618022 | |||||||
| chr13:26618076 | A | C | 4 | a0001c0001t0002g0043 a0001c0001t0002g0053 a0001c0001t0002g0067 others(1): Show |
4 | NA18952.hp2 NA18969.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+5018A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618076 | |||||||
| chr13:26618093 | A | T | 3 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 |
3 | HG01109.hp2 HG02145.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-11+5035A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618093 | |||||||
| chr13:26618133 | C | T | 1 | a0001c0001t0002g0282 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-11+5075C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618133 | |||||||
| chr13:26618259 | A | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0137 a0001c0001t0001g0141 |
3 | HG01928.hp2 HG01934.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-11+5201A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618259 | |||||||
| chr13:26618473 | T | C | 2 | a0001c0002t0003g0037 a0001c0002t0003g0038 |
2 | HG01074.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-11+5415T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618473 | |||||||
| chr13:26618481 | G | A | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(1): Show |
4 | HG02080.hp2 HG02132.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+5423G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618481 | |||||||
| chr13:26618496 | G | GC | 9 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0014g0118 others(6): Show |
9 | HG02027.hp2 HG02074.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+5445dupC | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26618496 | ||||||
| chr13:26618510 | T | G | 3 | a0001c0001t0002g0283 a0001c0001t0002g0285 a0001c0001t0002g0289 |
3 | NA18960.hp2 NA18961.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-11+5452T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618510 | |||||||
| chr13:26618516 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-11+5458C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618516 | |||||||
| chr13:26618524 | A | C | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-11+5466A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618524 | |||||||
| chr13:26618679 | T | C | 1 | a0001c0001t0007g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11+5621T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618679 | |||||||
| chr13:26618779 | A | G | 1 | a0001c0002t0004g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-11+5721A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618779 | |||||||
| chr13:26618842 | T | TTTGTATT others(36): Show |
1 | a0001c0001t0002g0065 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-11+5787_-11+5829d others(45): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26618842 | ||||||
| chr13:26618947 | T | A | 1 | a0001c0001t0014g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-11+5889T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618947 | |||||||
| chr13:26618979 | T | G | 74 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(71): Show |
74 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+5921T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618979 | |||||||
| chr13:26618992 | A | G | 5 | a0001c0002t0004g0021 a0001c0002t0004g0022 a0001c0002t0018g0020 others(2): Show |
5 | HG01175.hp1 HG01243.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+5934A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26618992 | |||||||
| chr13:26619196 | C | T | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11+6138C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26619196 | |||||||
| chr13:26619340 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-11+6282G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26619340 | |||||||
| chr13:26619400 | A | G | 1 | a0001c0001t0014g0143 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-11+6342A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26619400 | |||||||
| chr13:26619456 | C | G | 74 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(71): Show |
74 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+6398C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26619456 | |||||||
| chr13:26619464 | C | T | 1 | a0001c0002t0006g0246 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-11+6406C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26619464 | |||||||
| chr13:26619472 | A | C | 3 | a0002c0003t0011g0011 a0002c0003t0011g0012 a0002c0003t0011g0013 |
3 | HG02109.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-11+6414A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26619472 | |||||||
| chr13:26619651 | AC | A | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11+6594delC | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26619651 | |||||||
| chr13:26619749 | C | T | 31 | a0001c0001t0001g0036 a0001c0002t0004g0223 a0001c0002t0004g0224 others(28): Show |
31 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.-11+6691C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26619749 | |||||||
| chr13:26620090 | CTT | C | 6 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+7034_-11+7035d others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26620090 | ||||||
| chr13:26620124 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-11+7066T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26620124 | |||||||
| chr13:26620400 | G | A | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+7342G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26620400 | |||||||
| chr13:26620588 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.-11+7530A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26620588 | |||||||
| chr13:26620639 | A | G | 1 | a0001c0004t0013g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11+7581A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26620639 | |||||||
| chr13:26620676 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-11+7618C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26620676 | |||||||
| chr13:26620920 | G | T | 1 | a0001c0002t0009g0208 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-11+7862G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26620920 | |||||||
| chr13:26620922 | C | T | 74 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(71): Show |
74 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+7864C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26620922 | |||||||
| chr13:26621042 | A | G | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-11+7984A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26621042 | |||||||
| chr13:26621098 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-11+8040C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26621098 | |||||||
| chr13:26621256 | G | A | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-11+8198G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26621256 | |||||||
| chr13:26621269 | T | C | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+8211T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26621269 | |||||||
| chr13:26621339 | A | C | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+8281A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26621339 | |||||||
| chr13:26621377 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-11+8319A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26621377 | |||||||
| chr13:26621435 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-11+8377G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26621435 | |||||||
| chr13:26621445 | AGAAGAAA others(17): Show |
A | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11+8421_-11+8444d others(26): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26621445 | ||||||
| chr13:26621546 | C | A | 1 | a0001c0001t0002g0076 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-11+8488C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26621546 | |||||||
| chr13:26621572 | T | C | 1 | a0001c0002t0004g0235 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-11+8514T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26621572 | |||||||
| chr13:26621657 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-11+8599A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26621657 | |||||||
| chr13:26621754 | C | G | 3 | a0002c0003t0011g0011 a0002c0003t0011g0012 a0002c0003t0011g0013 |
3 | HG02109.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-11+8696C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26621754 | |||||||
| chr13:26621822 | T | C | 1 | a0001c0004t0013g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11+8764T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26621822 | |||||||
| chr13:26621879 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0164 |
2 | HG01255.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-11+8821G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26621879 | |||||||
| chr13:26622012 | G | A | 8 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
8 | HG00423.hp2 HG02071.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+8954G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26622012 | |||||||
| chr13:26622097 | T | G | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+9039T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26622097 | |||||||
| chr13:26622136 | G | A | 2 | a0001c0001t0005g0261 a0001c0001t0005g0262 |
2 | HG01255.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-11+9078G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26622136 | |||||||
| chr13:26622362 | T | A | 5 | a0002c0003t0003g0048 a0002c0003t0003g0070 a0002c0003t0003g0080 others(2): Show |
5 | HG01069.hp1 HG02148.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+9304T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26622362 | |||||||
| chr13:26622457 | G | A | 6 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+9399G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26622457 | |||||||
| chr13:26622727 | A | T | 1 | a0001c0001t0001g0126 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-11+9669A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26622727 | |||||||
| chr13:26622774 | CA | C | 18 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(15): Show |
18 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.-11+9729delA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26622774 | ||||||
| chr13:26622993 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-11+9935G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26622993 | |||||||
| chr13:26623282 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(110): Show |
113 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-11+10224G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26623282 | |||||||
| chr13:26623412 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-11+10354C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26623412 | |||||||
| chr13:26623579 | G | A | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+10521G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26623579 | |||||||
| chr13:26623638 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.-11+10580T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26623638 | |||||||
| chr13:26623873 | T | TA | 10 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0006g0030 others(7): Show |
10 | HG01074.hp1 HG01192.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+10816dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26623873 | ||||||
| chr13:26623941 | A | G | 4 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+10883A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26623941 | |||||||
| chr13:26624033 | G | A | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+10975G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26624033 | |||||||
| chr13:26624040 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11+10982T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26624040 | |||||||
| chr13:26624116 | G | A | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+11058G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26624116 | |||||||
| chr13:26624328 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-11+11270T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26624328 | |||||||
| chr13:26624444 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0158 |
2 | NA18979.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-11+11386G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26624444 | |||||||
| chr13:26624596 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-11+11538A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26624596 | |||||||
| chr13:26624631 | C | A | 4 | a0001c0002t0009g0205 a0001c0002t0009g0208 a0001c0002t0009g0209 others(1): Show |
4 | HG02145.hp1 HG03195.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+11573C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26624631 | |||||||
| chr13:26625026 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-11+11968G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26625026 | |||||||
| chr13:26625027 | G | A | 1 | a0001c0002t0011g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-11+11969G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26625027 | |||||||
| chr13:26625057 | C | T | 3 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 |
3 | HG02717.hp2 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-11+11999C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26625057 | |||||||
| chr13:26625138 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+12080A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26625138 | |||||||
| chr13:26625181 | C | T | 1 | a0001c0002t0028g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-11+12123C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26625181 | |||||||
| chr13:26625258 | G | A | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11+12200G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26625258 | |||||||
| chr13:26625285 | T | C | 102 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(99): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-11+12227T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26625285 | |||||||
| chr13:26625338 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11+12280G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26625338 | |||||||
| chr13:26625793 | G | A | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-11+12735G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26625793 | |||||||
| chr13:26625869 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(114): Show |
117 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-11+12811T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26625869 | |||||||
| chr13:26626015 | T | C | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-11+12957T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26626015 | |||||||
| chr13:26626102 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(100): Show |
103 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-11+13044A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26626102 | |||||||
| chr13:26626134 | G | A | 1 | a0001c0001t0012g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-11+13076G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26626134 | |||||||
| chr13:26626254 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0161 |
2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-11+13196T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26626254 | |||||||
| chr13:26626362 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+13304A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26626362 | |||||||
| chr13:26626375 | G | A | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-11+13317G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26626375 | |||||||
| chr13:26626625 | T | C | 1 | a0002c0003t0003g0056 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-11+13567T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26626625 | |||||||
| chr13:26626759 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-11+13701A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26626759 | |||||||
| chr13:26626827 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-11+13769A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26626827 | |||||||
| chr13:26626846 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-11+13788C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26626846 | |||||||
| chr13:26626972 | G | A | 120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-11+13914G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26626972 | |||||||
| chr13:26626990 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-11+13932T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26626990 | |||||||
| chr13:26627012 | CAAGAAAG | C | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+13955_-11+1396 others(11): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627012 | |||||||
| chr13:26627017 | A | G | 40 | a0001c0001t0002g0002 a0001c0001t0002g0253 a0001c0001t0002g0272 others(37): Show |
41 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-11+13959A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627017 | |||||||
| chr13:26627037 | A | G | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11+13979A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627037 | |||||||
| chr13:26627099 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11+14041A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627099 | |||||||
| chr13:26627225 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-11+14167T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627225 | |||||||
| chr13:26627269 | CT | C | 107 | a0001c0001t0001g0036 a0001c0001t0001g0131 a0001c0001t0001g0132 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.-11+14221delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26627269 | ||||||
| chr13:26627327 | G | A | 1 | a0001c0002t0003g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-11+14269G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627327 | |||||||
| chr13:26627349 | G | C | 1 | a0001c0002t0004g0225 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-11+14291G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627349 | |||||||
| chr13:26627431 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(103): Show |
106 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-11+14373A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627431 | |||||||
| chr13:26627572 | G | T | 1 | a0001c0002t0016g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-11+14514G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627572 | |||||||
| chr13:26627663 | A | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-14598A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627663 | |||||||
| chr13:26627677 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(103): Show |
106 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-10-14584A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627677 | |||||||
| chr13:26627683 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-10-14578G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627683 | |||||||
| chr13:26627866 | C | T | 3 | a0002c0003t0003g0098 a0002c0003t0003g0099 a0002c0003t0003g0201 |
3 | HG01891.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-10-14395C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627866 | |||||||
| chr13:26627881 | TATA | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(103): Show |
106 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-10-14372_-10-1437 others(7): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26627881 | ||||||
| chr13:26627893 | GA | G | 19 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10-14359delA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26627893 | ||||||
| chr13:26627911 | AT | A | 12 | a0001c0001t0001g0036 a0001c0001t0001g0112 a0001c0001t0001g0121 others(9): Show |
12 | HG00673.hp1 HG01070.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10-14349delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627911 | |||||||
| chr13:26627912 | T | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(265): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-10-14349T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627912 | |||||||
| chr13:26627917 | T | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(111): Show |
114 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-10-14344T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26627917 | |||||||
| chr13:26628042 | C | T | 5 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0076 others(2): Show |
5 | HG00558.hp2 NA19056.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-14219C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26628042 | |||||||
| chr13:26628053 | TGGAAATG others(7): Show |
T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(122): Show |
125 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-10-14205_-10-1419 others(18): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26628053 | ||||||
| chr13:26628324 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-10-13937A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26628324 | |||||||
| chr13:26628362 | A | G | 3 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0136 |
3 | HG01943.hp1 HG01975.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-10-13899A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26628362 | |||||||
| chr13:26628366 | A | G | 6 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-13895A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26628366 | |||||||
| chr13:26628442 | G | C | 65 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(62): Show |
65 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-10-13819G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26628442 | |||||||
| chr13:26628645 | T | C | 6 | a0001c0002t0009g0003 a0001c0002t0009g0207 a0001c0002t0009g0211 others(3): Show |
6 | HG02055.hp1 HG03041.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-13616T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26628645 | |||||||
| chr13:26628883 | C | A | 19 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10-13378C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26628883 | |||||||
| chr13:26628894 | C | T | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-13367C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26628894 | |||||||
| chr13:26628909 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-10-13352A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26628909 | |||||||
| chr13:26628947 | G | C | 99 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-10-13314G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26628947 | |||||||
| chr13:26629116 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-13145C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26629116 | |||||||
| chr13:26629252 | G | A | 4 | a0001c0002t0009g0205 a0001c0002t0009g0208 a0001c0002t0009g0209 others(1): Show |
4 | HG02145.hp1 HG03195.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-13009G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26629252 | |||||||
| chr13:26629258 | C | T | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10-13003C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26629258 | |||||||
| chr13:26629377 | GT | G | 66 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(63): Show |
66 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.-10-12882delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26629377 | ||||||
| chr13:26629512 | T | G | 1 | a0001c0002t0009g0209 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10-12749T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26629512 | |||||||
| chr13:26629685 | GC | G | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10-12575delC | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26629685 | |||||||
| chr13:26629700 | G | C | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10-12561G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26629700 | |||||||
| chr13:26629894 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-10-12367C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26629894 | |||||||
| chr13:26629925 | T | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(114): Show |
117 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-10-12336T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26629925 | |||||||
| chr13:26629934 | C | T | 1 | a0001c0001t0002g0273 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-10-12327C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26629934 | |||||||
| chr13:26630324 | A | G | 124 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-10-11937A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26630324 | |||||||
| chr13:26630440 | GAGA | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-11818_-10-1181 others(7): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26630440 | ||||||
| chr13:26630507 | G | A | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10-11754G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26630507 | |||||||
| chr13:26630608 | C | T | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10-11653C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26630608 | |||||||
| chr13:26630618 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-11643A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26630618 | |||||||
| chr13:26630635 | T | C | 101 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-10-11626T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26630635 | |||||||
| chr13:26630665 | G | A | 4 | a0001c0002t0004g0226 a0001c0002t0004g0230 a0001c0002t0004g0236 others(1): Show |
4 | HG00099.hp1 HG01069.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-11596G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26630665 | |||||||
| chr13:26630685 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(115): Show |
118 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-10-11576T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26630685 | |||||||
| chr13:26630687 | G | A | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-11574G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26630687 | |||||||
| chr13:26630707 | T | TA | 19 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0061 others(16): Show |
19 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10-11553dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26630707 | ||||||
| chr13:26630881 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-10-11380G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26630881 | |||||||
| chr13:26630918 | G | A | 6 | a0001c0002t0009g0003 a0001c0002t0009g0207 a0001c0002t0009g0211 others(3): Show |
6 | HG02055.hp1 HG03041.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-11343G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26630918 | |||||||
| chr13:26631096 | C | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-10-11165C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26631096 | |||||||
| chr13:26631120 | T | C | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-11141T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26631120 | |||||||
| chr13:26631168 | A | G | 40 | a0001c0001t0002g0002 a0001c0001t0002g0253 a0001c0001t0002g0272 others(37): Show |
41 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-10-11093A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26631168 | |||||||
| chr13:26631172 | G | C | 3 | a0002c0003t0011g0011 a0002c0003t0011g0012 a0002c0003t0011g0013 |
3 | HG02109.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-10-11089G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26631172 | |||||||
| chr13:26631231 | C | T | 4 | a0001c0001t0005g0264 a0001c0001t0005g0268 a0001c0001t0005g0269 others(1): Show |
4 | HG01081.hp2 HG01169.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-11030C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26631231 | |||||||
| chr13:26631250 | C | G | 1 | a0001c0001t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10-11011C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26631250 | |||||||
| chr13:26631733 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(99): Show |
102 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-10-10528A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26631733 | |||||||
| chr13:26631752 | T | C | 25 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(22): Show |
25 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-10-10509T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26631752 | |||||||
| chr13:26631878 | C | G | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-10383C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26631878 | |||||||
| chr13:26631992 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-10269G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26631992 | |||||||
| chr13:26632014 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-10-10247G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26632014 | |||||||
| chr13:26632018 | A | G | 2 | a0001c0001t0010g0027 a0001c0001t0022g0168 |
2 | HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-10-10243A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26632018 | |||||||
| chr13:26632065 | A | T | 1 | a0001c0001t0001g0151 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-10-10196A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26632065 | |||||||
| chr13:26632078 | A | T | 1 | a0001c0001t0001g0151 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-10-10183A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26632078 | |||||||
| chr13:26632225 | A | G | 1 | a0001c0001t0005g0265 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-10-10036A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26632225 | |||||||
| chr13:26632388 | T | C | 2 | a0001c0002t0003g0037 a0001c0002t0003g0038 |
2 | HG01074.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-10-9873T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26632388 | |||||||
| chr13:26632488 | A | T | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10-9773A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26632488 | |||||||
| chr13:26632774 | A | G | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10-9487A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26632774 | |||||||
| chr13:26633021 | C | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-9240C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26633021 | |||||||
| chr13:26633200 | C | CT | 8 | a0001c0001t0001g0140 a0001c0001t0001g0159 a0001c0001t0002g0239 others(5): Show |
8 | HG00544.hp2 HG00738.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-9045dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26633200 | ||||||
| chr13:26633200 | C | CTT | 120 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(117): Show |
120 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-10-9046_-10-9045d others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26633200 | ||||||
| chr13:26633200 | C | CTTTTTTT | 12 | a0001c0001t0002g0071 a0001c0001t0008g0019 a0001c0002t0009g0003 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-9051_-10-9045d others(9): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26633200 | ||||||
| chr13:26633200 | C | CTTTTTTT others(1): Show |
61 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(58): Show |
61 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.-10-9052_-10-9045d others(10): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26633200 | ||||||
| chr13:26633200 | C | CTTTTTTT others(2): Show |
47 | a0001c0001t0002g0002 a0001c0001t0002g0043 a0001c0001t0002g0253 others(44): Show |
48 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.-10-9053_-10-9045d others(11): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26633200 | ||||||
| chr13:26633200 | C | CTTTTTTT others(3): Show |
18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(15): Show |
18 | HG00639.hp2 HG01069.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-10-9054_-10-9045d others(12): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26633200 | ||||||
| chr13:26633200 | C | CTTTTTTT others(4): Show |
13 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(10): Show |
13 | HG00099.hp1 HG00280.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-9055_-10-9045d others(13): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26633200 | ||||||
| chr13:26633200 | C | CTTTTTTT others(5): Show |
3 | a0001c0002t0004g0240 a0001c0002t0017g0229 a0001c0002t0017g0232 |
3 | HG01081.hp1 HG01515.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-10-9056_-10-9045d others(14): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26633200 | ||||||
| chr13:26633262 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-10-8999G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26633262 | |||||||
| chr13:26633264 | GTCATC | G | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-8993_-10-8989d others(7): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26633264 | ||||||
| chr13:26633323 | C | G | 6 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-8938C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26633323 | |||||||
| chr13:26633347 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-10-8914C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26633347 | |||||||
| chr13:26633363 | C | T | 3 | a0001c0001t0001g0108 a0003c0005t0008g0251 a0003c0005t0008g0252 |
3 | HG01496.hp1 HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-10-8898C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26633363 | |||||||
| chr13:26633392 | T | C | 99 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-10-8869T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26633392 | |||||||
| chr13:26633446 | T | C | 111 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-10-8815T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26633446 | |||||||
| chr13:26633455 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(115): Show |
118 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-10-8806C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26633455 | |||||||
| chr13:26633462 | C | T | 1 | a0001c0004t0013g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-10-8799C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26633462 | |||||||
| chr13:26633664 | G | A | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10-8597G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26633664 | |||||||
| chr13:26633674 | G | T | 1 | a0001c0002t0003g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-10-8587G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26633674 | |||||||
| chr13:26633888 | C | G | 2 | a0001c0001t0002g0039 a0001c0001t0002g0042 |
2 | NA18942.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-10-8373C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26633888 | |||||||
| chr13:26634061 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-10-8200C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634061 | |||||||
| chr13:26634062 | G | A | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-8199G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634062 | |||||||
| chr13:26634154 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-10-8107T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634154 | |||||||
| chr13:26634186 | A | G | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-8075A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634186 | |||||||
| chr13:26634275 | T | G | 1 | a0001c0001t0015g0015 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-10-7986T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634275 | |||||||
| chr13:26634299 | A | G | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-7962A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634299 | |||||||
| chr13:26634335 | C | T | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-7926C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634335 | |||||||
| chr13:26634534 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 |
3 | HG01109.hp2 HG02145.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-10-7727G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634534 | |||||||
| chr13:26634551 | A | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-10-7710A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634551 | |||||||
| chr13:26634561 | G | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(122): Show |
125 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-10-7700G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634561 | |||||||
| chr13:26634583 | G | A | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-7678G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634583 | |||||||
| chr13:26634804 | G | C | 2 | a0002c0003t0003g0099 a0002c0003t0003g0201 |
2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-10-7457G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634804 | |||||||
| chr13:26634878 | C | T | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-10-7383C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634878 | |||||||
| chr13:26634893 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(117): Show |
120 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-10-7368G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634893 | |||||||
| chr13:26634964 | C | T | 64 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(61): Show |
64 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-10-7297C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26634964 | |||||||
| chr13:26635243 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-7018C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26635243 | |||||||
| chr13:26635301 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG00639.hp2 HG02055.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-6960G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26635301 | |||||||
| chr13:26635482 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-10-6779G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26635482 | |||||||
| chr13:26635496 | G | A | 64 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(61): Show |
64 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-10-6765G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26635496 | |||||||
| chr13:26635511 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG00639.hp2 HG01243.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-6750C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26635511 | |||||||
| chr13:26635705 | T | C | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-6556T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26635705 | |||||||
| chr13:26635793 | C | T | 4 | a0001c0001t0005g0264 a0001c0001t0005g0268 a0001c0001t0005g0269 others(1): Show |
4 | HG01081.hp2 HG01169.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-6468C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26635793 | |||||||
| chr13:26635816 | C | T | 1 | a0001c0001t0020g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-10-6445C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26635816 | |||||||
| chr13:26635903 | G | A | 6 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-6358G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26635903 | |||||||
| chr13:26635996 | G | A | 1 | a0002c0003t0003g0051 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-10-6265G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26635996 | |||||||
| chr13:26636063 | T | C | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-6198T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636063 | |||||||
| chr13:26636182 | C | T | 99 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-10-6079C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636182 | |||||||
| chr13:26636184 | G | A | 25 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(22): Show |
25 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-10-6077G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636184 | |||||||
| chr13:26636210 | C | T | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-6051C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636210 | |||||||
| chr13:26636233 | CCT | C | 6 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-6027_-10-6026d others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636233 | |||||||
| chr13:26636296 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-5965G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636296 | |||||||
| chr13:26636313 | C | T | 74 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(71): Show |
74 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-10-5948C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636313 | |||||||
| chr13:26636325 | G | A | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10-5936G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636325 | |||||||
| chr13:26636384 | C | T | 1 | a0001c0002t0016g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-10-5877C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636384 | |||||||
| chr13:26636396 | G | T | 1 | a0001c0001t0012g0192 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-10-5865G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636396 | |||||||
| chr13:26636537 | A | G | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-5724A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636537 | |||||||
| chr13:26636588 | G | A | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-5673G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636588 | |||||||
| chr13:26636677 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10-5584A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636677 | |||||||
| chr13:26636788 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(101): Show |
104 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-10-5473G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636788 | |||||||
| chr13:26636873 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-10-5388T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26636873 | |||||||
| chr13:26636874 | T | TG | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-5382dupG | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26636874 | ||||||
| chr13:26637003 | C | T | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-5258C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26637003 | |||||||
| chr13:26637005 | C | T | 1 | a0001c0002t0006g0034 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-10-5256C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26637005 | |||||||
| chr13:26637231 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-10-5030C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26637231 | |||||||
| chr13:26637411 | G | A | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10-4850G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26637411 | |||||||
| chr13:26637433 | GCTCTTA | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-4823_-10-4818d others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26637433 | ||||||
| chr13:26637514 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0179 |
2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-10-4747C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26637514 | |||||||
| chr13:26637587 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-4674G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26637587 | |||||||
| chr13:26637731 | A | G | 1 | a0001c0001t0002g0281 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-10-4530A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26637731 | |||||||
| chr13:26637732 | G | C | 2 | a0001c0002t0011g0215 a0001c0002t0011g0216 |
2 | HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-10-4529G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26637732 | |||||||
| chr13:26637818 | A | G | 1 | a0001c0002t0006g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-10-4443A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26637818 | |||||||
| chr13:26637868 | A | G | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-4393A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26637868 | |||||||
| chr13:26637894 | G | C | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-4367G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26637894 | |||||||
| chr13:26638028 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 |
3 | HG01109.hp2 HG02145.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-10-4233C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26638028 | |||||||
| chr13:26638047 | A | C | 2 | a0002c0003t0003g0049 a0002c0003t0003g0050 |
2 | HG02523.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-10-4214A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26638047 | |||||||
| chr13:26638078 | C | G | 101 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-10-4183C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26638078 | |||||||
| chr13:26638703 | C | T | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10-3558C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26638703 | |||||||
| chr13:26638797 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0200 |
2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-10-3464C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26638797 | |||||||
| chr13:26638814 | G | T | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-3447G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26638814 | |||||||
| chr13:26639044 | G | A | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-3217G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26639044 | |||||||
| chr13:26639364 | G | C | 99 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-10-2897G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26639364 | |||||||
| chr13:26639421 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-2840C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26639421 | |||||||
| chr13:26639428 | C | T | 19 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10-2833C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26639428 | |||||||
| chr13:26639631 | G | T | 99 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-10-2630G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26639631 | |||||||
| chr13:26639657 | C | T | 6 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-2604C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26639657 | |||||||
| chr13:26639721 | G | A | 9 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0002g0284 others(6): Show |
9 | NA18612.hp2 NA18941.hp2 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-2540G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26639721 | |||||||
| chr13:26639785 | C | G | 1 | a0001c0001t0002g0170 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-10-2476C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26639785 | |||||||
| chr13:26639788 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-10-2473G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26639788 | |||||||
| chr13:26639811 | G | C | 3 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0169 |
3 | HG01891.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-10-2450G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26639811 | |||||||
| chr13:26639914 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-10-2347G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26639914 | |||||||
| chr13:26639945 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(106): Show |
109 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-10-2316T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26639945 | |||||||
| chr13:26640068 | G | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-10-2193G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26640068 | |||||||
| chr13:26640408 | CT | C | 27 | a0001c0001t0001g0016 a0001c0001t0001g0140 a0001c0001t0008g0249 others(24): Show |
27 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.-10-1840delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26640408 | ||||||
| chr13:26640409 | T | C | 1 | a0001c0002t0004g0240 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-10-1852T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26640409 | |||||||
| chr13:26640587 | T | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-10-1674T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26640587 | |||||||
| chr13:26640626 | C | T | 1 | a0001c0004t0024g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-10-1635C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26640626 | |||||||
| chr13:26640709 | T | C | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10-1552T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26640709 | |||||||
| chr13:26640777 | T | C | 113 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-10-1484T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26640777 | |||||||
| chr13:26640795 | T | TA | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-1465dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26640795 | ||||||
| chr13:26640797 | T | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-1464T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26640797 | |||||||
| chr13:26640798 | T | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-1463T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26640798 | |||||||
| chr13:26640976 | G | A | 40 | a0001c0001t0002g0002 a0001c0001t0002g0253 a0001c0001t0002g0272 others(37): Show |
41 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-10-1285G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26640976 | |||||||
| chr13:26640992 | C | G | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-1269C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26640992 | |||||||
| chr13:26641126 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-10-1135A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26641126 | |||||||
| chr13:26641256 | A | G | 1 | a0001c0002t0016g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-10-1005A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26641256 | |||||||
| chr13:26641263 | G | A | 1 | a0001c0002t0003g0038 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-10-998G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26641263 | |||||||
| chr13:26641284 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-10-977T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26641284 | |||||||
| chr13:26641369 | G | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-10-892G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26641369 | |||||||
| chr13:26641384 | G | A | 19 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10-877G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26641384 | |||||||
| chr13:26641547 | C | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-10-714C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26641547 | |||||||
| chr13:26641826 | A | G | 64 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(61): Show |
64 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-10-435A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26641826 | |||||||
| chr13:26642089 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-172A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | chr13 | 26642089 | |||||||
| chr13:26642099 | CTAAAG | C | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-158_-10-154del others(5): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 26642099 | ||||||
| chr13:26642492 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0158 |
2 | NA18979.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.133+89T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26642492 | |||||||
| chr13:26642589 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+186A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26642589 | |||||||
| chr13:26642610 | C | T | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+207C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26642610 | |||||||
| chr13:26642613 | A | G | 1 | a0001c0002t0026g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.133+210A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26642613 | |||||||
| chr13:26642747 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0121 a0001c0001t0029g0157 |
3 | HG00673.hp1 NA18941.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.133+344G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26642747 | |||||||
| chr13:26642803 | A | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(117): Show |
120 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.133+400A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26642803 | |||||||
| chr13:26642925 | A | G | 1 | a0002c0003t0003g0062 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.133+522A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26642925 | |||||||
| chr13:26642938 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(227): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.133+535T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26642938 | |||||||
| chr13:26642986 | C | T | 40 | a0001c0001t0002g0002 a0001c0001t0002g0253 a0001c0001t0002g0272 others(37): Show |
41 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.133+583C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26642986 | |||||||
| chr13:26643003 | A | C | 1 | a0001c0002t0004g0231 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.133+600A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26643003 | |||||||
| chr13:26643032 | G | T | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+629G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26643032 | |||||||
| chr13:26643178 | T | G | 18 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(15): Show |
18 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.133+775T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26643178 | |||||||
| chr13:26643276 | C | T | 99 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.133+873C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26643276 | |||||||
| chr13:26643389 | G | T | 3 | a0002c0003t0011g0011 a0002c0003t0011g0012 a0002c0003t0011g0013 |
3 | HG02109.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.133+986G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26643389 | |||||||
| chr13:26643398 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(117): Show |
120 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.133+995T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26643398 | |||||||
| chr13:26643454 | A | G | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.133+1051A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26643454 | |||||||
| chr13:26643574 | T | C | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.133+1171T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26643574 | |||||||
| chr13:26643582 | C | T | 2 | a0001c0004t0013g0033 a0001c0004t0013g0195 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.133+1179C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26643582 | |||||||
| chr13:26643659 | G | C | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+1256G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26643659 | |||||||
| chr13:26644065 | A | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+1662A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26644065 | |||||||
| chr13:26644099 | A | T | 2 | a0001c0001t0002g0079 a0001c0001t0002g0090 |
2 | HG00673.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.133+1696A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26644099 | |||||||
| chr13:26644430 | G | A | 3 | a0001c0001t0005g0268 a0001c0001t0005g0269 a0001c0001t0005g0270 |
3 | HG01081.hp2 HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.133+2027G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26644430 | |||||||
| chr13:26644541 | G | A | 1 | a0005c0006t0002g0057 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.133+2138G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26644541 | |||||||
| chr13:26644567 | G | A | 11 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0137 others(8): Show |
11 | HG00408.hp2 HG01070.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.133+2164G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26644567 | |||||||
| chr13:26644627 | G | A | 2 | a0001c0002t0003g0037 a0001c0002t0003g0038 |
2 | HG01074.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.133+2224G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26644627 | |||||||
| chr13:26644658 | G | A | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.133+2255G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26644658 | |||||||
| chr13:26644909 | G | A | 1 | a0001c0001t0002g0072 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.133+2506G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26644909 | |||||||
| chr13:26644980 | T | G | 25 | a0001c0001t0001g0112 a0001c0001t0001g0120 a0001c0001t0001g0121 others(22): Show |
25 | HG00423.hp2 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.133+2577T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26644980 | |||||||
| chr13:26645076 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.133+2673C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26645076 | |||||||
| chr13:26645131 | A | G | 18 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(15): Show |
18 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.133+2728A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26645131 | |||||||
| chr13:26645412 | T | C | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.133+3009T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26645412 | |||||||
| chr13:26645619 | G | A | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+3216G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26645619 | |||||||
| chr13:26645838 | T | G | 115 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.133+3435T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26645838 | |||||||
| chr13:26645937 | TC | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+3536delC | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26645937 | ||||||
| chr13:26646089 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.133+3686T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26646089 | |||||||
| chr13:26646181 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.133+3778C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26646181 | |||||||
| chr13:26646247 | A | G | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+3844A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26646247 | |||||||
| chr13:26646454 | G | T | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.133+4051G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26646454 | |||||||
| chr13:26646522 | C | G | 1 | a0001c0002t0004g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.133+4119C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26646522 | |||||||
| chr13:26646526 | C | G | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+4123C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26646526 | |||||||
| chr13:26646573 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+4170A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26646573 | |||||||
| chr13:26646664 | G | A | 1 | a0002c0003t0003g0062 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.133+4261G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26646664 | |||||||
| chr13:26646668 | C | T | 6 | a0001c0001t0020g0026 a0001c0002t0006g0242 a0001c0002t0006g0243 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+4265C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26646668 | |||||||
| chr13:26646738 | AG | A | 18 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(15): Show |
18 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.133+4337delG | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26646738 | ||||||
| chr13:26646860 | C | A | 1 | a0001c0001t0002g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.133+4457C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26646860 | |||||||
| chr13:26647069 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(113): Show |
116 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.133+4666G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26647069 | |||||||
| chr13:26647087 | C | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.133+4684C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26647087 | |||||||
| chr13:26647205 | GTT | G | 40 | a0001c0001t0002g0002 a0001c0001t0002g0253 a0001c0001t0002g0272 others(37): Show |
41 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.133+4804_133+4805d others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26647205 | ||||||
| chr13:26647288 | G | A | 2 | a0002c0003t0011g0011 a0002c0003t0011g0012 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.133+4885G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26647288 | |||||||
| chr13:26647342 | C | T | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+4939C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26647342 | |||||||
| chr13:26647343 | G | A | 103 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(100): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.133+4940G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26647343 | |||||||
| chr13:26647833 | CAA | C | 5 | a0001c0002t0006g0242 a0001c0002t0006g0243 a0001c0002t0006g0244 others(2): Show |
5 | HG02258.hp1 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+5433_133+5434d others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26647833 | ||||||
| chr13:26647971 | TAA | T | 18 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(15): Show |
18 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.133+5569_133+5570d others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26647971 | |||||||
| chr13:26647987 | A | G | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.133+5584A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26647987 | |||||||
| chr13:26647994 | G | T | 103 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(100): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.133+5591G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26647994 | |||||||
| chr13:26648023 | T | C | 12 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0006g0030 others(9): Show |
12 | HG00738.hp2 HG01074.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.133+5620T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26648023 | |||||||
| chr13:26648163 | G | C | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+5760G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26648163 | |||||||
| chr13:26648301 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+5898A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26648301 | |||||||
| chr13:26648543 | T | C | 1 | a0002c0003t0003g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.133+6140T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26648543 | |||||||
| chr13:26648794 | A | G | 2 | a0001c0002t0004g0223 a0001c0002t0004g0224 |
2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.133+6391A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26648794 | |||||||
| chr13:26648903 | C | T | 8 | a0001c0001t0001g0108 a0001c0001t0007g0045 a0001c0001t0007g0085 others(5): Show |
8 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.133+6500C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26648903 | |||||||
| chr13:26648941 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.133+6538G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26648941 | |||||||
| chr13:26649033 | T | C | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+6630T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26649033 | |||||||
| chr13:26649069 | T | C | 1 | a0001c0001t0002g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.133+6666T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26649069 | |||||||
| chr13:26649192 | G | A | 18 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(15): Show |
18 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.133+6789G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26649192 | |||||||
| chr13:26649378 | A | T | 6 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+6975A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26649378 | |||||||
| chr13:26649396 | T | C | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.133+6993T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26649396 | |||||||
| chr13:26649446 | C | T | 64 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(61): Show |
64 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.133+7043C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26649446 | |||||||
| chr13:26649607 | G | C | 4 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+7204G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26649607 | |||||||
| chr13:26649636 | G | A | 101 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.133+7233G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26649636 | |||||||
| chr13:26649709 | C | T | 101 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.133+7306C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26649709 | |||||||
| chr13:26649745 | C | A | 1 | a0001c0001t0007g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.133+7342C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26649745 | |||||||
| chr13:26649870 | G | GACC | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+7469_133+7471d others(5): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26649870 | ||||||
| chr13:26649899 | G | A | 101 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.133+7496G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26649899 | |||||||
| chr13:26649907 | A | T | 9 | a0001c0001t0001g0108 a0001c0001t0007g0044 a0001c0001t0007g0045 others(6): Show |
9 | HG01496.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.133+7504A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26649907 | |||||||
| chr13:26649911 | AAAT | A | 4 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+7510_133+7512d others(5): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26649911 | ||||||
| chr13:26650156 | T | A | 2 | a0001c0002t0016g0010 a0001c0002t0016g0014 |
2 | HG00738.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.133+7753T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26650156 | |||||||
| chr13:26650433 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+8030A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26650433 | |||||||
| chr13:26650537 | T | C | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+8134T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26650537 | |||||||
| chr13:26650776 | G | A | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.133+8373G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26650776 | |||||||
| chr13:26650968 | T | A | 103 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(100): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.133+8565T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26650968 | |||||||
| chr13:26650975 | G | C | 1 | a0001c0002t0006g0032 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.133+8572G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26650975 | |||||||
| chr13:26651032 | G | A | 1 | a0001c0001t0038g0258 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.133+8629G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26651032 | |||||||
| chr13:26651129 | C | G | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.133+8726C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26651129 | |||||||
| chr13:26651133 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.133+8730C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26651133 | |||||||
| chr13:26651152 | A | C | 119 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.133+8749A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26651152 | |||||||
| chr13:26651331 | A | C | 1 | a0001c0001t0001g0148 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.133+8928A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26651331 | |||||||
| chr13:26651545 | C | A | 76 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0029 others(73): Show |
76 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.133+9142C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26651545 | |||||||
| chr13:26651736 | C | T | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+9333C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26651736 | |||||||
| chr13:26651966 | A | G | 11 | a0001c0001t0001g0112 a0001c0001t0001g0120 a0001c0001t0001g0121 others(8): Show |
11 | HG00423.hp2 HG00673.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.133+9563A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26651966 | |||||||
| chr13:26652152 | A | G | 1 | a0001c0002t0004g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.133+9749A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26652152 | |||||||
| chr13:26652208 | G | T | 53 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(50): Show |
53 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.133+9805G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26652208 | |||||||
| chr13:26652219 | A | G | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.133+9816A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26652219 | |||||||
| chr13:26652485 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.133+10082A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26652485 | |||||||
| chr13:26652545 | C | A | 29 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0007g0044 others(26): Show |
29 | HG00423.hp1 HG01069.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.133+10142C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26652545 | |||||||
| chr13:26652859 | A | G | 7 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0131 others(4): Show |
7 | HG02056.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.133+10456A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26652859 | |||||||
| chr13:26652911 | TA | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.133+10509delA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26652911 | |||||||
| chr13:26652939 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.133+10536C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26652939 | |||||||
| chr13:26652940 | G | A | 1 | a0001c0001t0002g0288 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.133+10537G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26652940 | |||||||
| chr13:26653041 | T | G | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+10638T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26653041 | |||||||
| chr13:26653187 | A | G | 1 | a0001c0001t0037g0292 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.133+10784A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26653187 | |||||||
| chr13:26653285 | T | C | 62 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(59): Show |
62 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.133+10882T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26653285 | |||||||
| chr13:26653497 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.133+11094C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26653497 | |||||||
| chr13:26653744 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(97): Show |
100 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.134-11284A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26653744 | |||||||
| chr13:26653910 | C | G | 13 | a0001c0002t0006g0030 a0001c0002t0006g0031 a0001c0002t0006g0032 others(10): Show |
13 | HG01192.hp1 HG02148.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.134-11118C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26653910 | |||||||
| chr13:26653927 | CCTAT | C | 4 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-11098_134-1109 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26653927 | ||||||
| chr13:26654055 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(111): Show |
114 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.134-10973G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26654055 | |||||||
| chr13:26654077 | T | TGTCA | 8 | a0001c0001t0007g0044 a0001c0001t0007g0045 a0001c0001t0007g0085 others(5): Show |
8 | HG02809.hp2 HG02818.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-10950_134-1094 others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26654077 | ||||||
| chr13:26654150 | G | A | 1 | a0001c0002t0004g0228 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.134-10878G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26654150 | |||||||
| chr13:26654184 | G | T | 1 | a0001c0001t0005g0264 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.134-10844G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26654184 | |||||||
| chr13:26654207 | C | A | 6 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-10821C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26654207 | |||||||
| chr13:26654401 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(109): Show |
112 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.134-10627T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26654401 | |||||||
| chr13:26654435 | G | A | 63 | a0001c0001t0002g0047 a0001c0002t0003g0037 a0001c0002t0003g0038 others(60): Show |
63 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.134-10593G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26654435 | |||||||
| chr13:26654486 | C | T | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-10542C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26654486 | |||||||
| chr13:26654632 | T | G | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-10396T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26654632 | |||||||
| chr13:26654757 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.134-10271A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26654757 | |||||||
| chr13:26655205 | GACTTTTA others(10): Show |
G | 3 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 |
3 | HG01109.hp2 HG02145.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.134-9783_134-9767d others(19): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26655205 | ||||||
| chr13:26655275 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 |
3 | HG01109.hp2 HG02145.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.134-9753C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26655275 | |||||||
| chr13:26655324 | G | A | 2 | a0001c0001t0020g0026 a0001c0002t0031g0214 |
2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.134-9704G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26655324 | |||||||
| chr13:26655374 | C | T | 5 | a0001c0001t0002g0272 a0001c0001t0002g0277 a0001c0001t0002g0278 others(2): Show |
5 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-9654C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26655374 | |||||||
| chr13:26655463 | G | T | 4 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-9565G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26655463 | |||||||
| chr13:26655657 | C | T | 62 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(59): Show |
62 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.134-9371C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26655657 | |||||||
| chr13:26655892 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.134-9136G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26655892 | |||||||
| chr13:26655953 | C | T | 23 | a0001c0002t0004g0021 a0001c0002t0004g0022 a0001c0002t0004g0223 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.134-9075C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26655953 | |||||||
| chr13:26655991 | T | A | 4 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0010g0220 others(1): Show |
4 | HG01099.hp2 HG02602.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-9037T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26655991 | |||||||
| chr13:26655993 | G | A | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.134-9035G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26655993 | |||||||
| chr13:26656466 | T | A | 62 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(59): Show |
62 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.134-8562T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26656466 | |||||||
| chr13:26656758 | T | C | 1 | a0001c0002t0006g0030 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.134-8270T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26656758 | |||||||
| chr13:26656766 | A | G | 18 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(15): Show |
18 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.134-8262A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26656766 | |||||||
| chr13:26656795 | A | C | 1 | a0001c0004t0013g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.134-8233A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26656795 | |||||||
| chr13:26656844 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.134-8184A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26656844 | |||||||
| chr13:26656872 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.134-8156C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26656872 | |||||||
| chr13:26656950 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.134-8078T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26656950 | |||||||
| chr13:26657075 | C | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(101): Show |
104 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.134-7953C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26657075 | |||||||
| chr13:26657469 | A | G | 4 | a0001c0001t0012g0191 a0001c0001t0012g0192 a0001c0001t0012g0193 others(1): Show |
4 | HG01168.hp1 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-7559A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26657469 | |||||||
| chr13:26657899 | A | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.134-7129A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26657899 | |||||||
| chr13:26657909 | T | C | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-7119T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26657909 | |||||||
| chr13:26657993 | G | A | 3 | a0001c0001t0002g0277 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02486.hp1 HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.134-7035G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26657993 | |||||||
| chr13:26658025 | T | G | 73 | a0001c0001t0008g0019 a0001c0002t0003g0037 a0001c0002t0003g0038 others(70): Show |
73 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.134-7003T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26658025 | |||||||
| chr13:26658126 | G | A | 35 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(32): Show |
35 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.134-6902G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26658126 | |||||||
| chr13:26658134 | GTA | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(284): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.134-6891_134-6890d others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26658134 | ||||||
| chr13:26658272 | G | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(110): Show |
113 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.134-6756G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26658272 | |||||||
| chr13:26658378 | C | G | 1 | a0001c0001t0005g0266 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.134-6650C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26658378 | |||||||
| chr13:26658427 | C | T | 23 | a0001c0002t0004g0021 a0001c0002t0004g0022 a0001c0002t0004g0223 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.134-6601C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26658427 | |||||||
| chr13:26658642 | G | T | 1 | a0001c0002t0019g0217 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.134-6386G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26658642 | |||||||
| chr13:26658899 | T | C | 66 | a0001c0001t0001g0135 a0001c0001t0001g0179 a0001c0002t0003g0037 others(63): Show |
66 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.134-6129T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26658899 | |||||||
| chr13:26658902 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.134-6126C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26658902 | |||||||
| chr13:26659455 | C | T | 3 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0096 |
3 | HG02129.hp1 HG02135.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.134-5573C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26659455 | |||||||
| chr13:26659643 | G | T | 23 | a0001c0002t0004g0021 a0001c0002t0004g0022 a0001c0002t0004g0223 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.134-5385G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26659643 | |||||||
| chr13:26659646 | T | C | 2 | a0001c0002t0003g0037 a0001c0002t0003g0038 |
2 | HG01074.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.134-5382T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26659646 | |||||||
| chr13:26659681 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0169 |
3 | HG01891.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.134-5347C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26659681 | |||||||
| chr13:26659734 | C | T | 3 | a0002c0003t0011g0011 a0002c0003t0011g0012 a0002c0003t0011g0013 |
3 | HG02109.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.134-5294C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26659734 | |||||||
| chr13:26659868 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.134-5160G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26659868 | |||||||
| chr13:26659892 | A | G | 4 | a0001c0001t0002g0039 a0001c0001t0002g0042 a0001c0001t0002g0097 others(1): Show |
4 | HG02015.hp2 NA18942.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-5136A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26659892 | |||||||
| chr13:26660136 | G | A | 3 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 |
3 | HG02717.hp2 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.134-4892G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26660136 | |||||||
| chr13:26660194 | G | GTTTTTTT others(3): Show |
1 | a0001c0004t0013g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.134-4808_134-4799d others(12): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660194 | G | GTTTTTTT others(7): Show |
2 | a0001c0004t0013g0195 a0001c0004t0013g0197 |
2 | HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.134-4812_134-4799d others(16): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660194 | GT | G | 7 | a0001c0001t0001g0016 a0001c0002t0004g0226 a0001c0002t0004g0228 others(4): Show |
7 | HG00099.hp1 HG01069.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-4799delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660194 | GTT | G | 6 | a0001c0001t0001g0102 a0001c0001t0001g0108 a0001c0001t0033g0100 others(3): Show |
6 | HG01496.hp1 HG01515.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-4800_134-4799d others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660194 | GTTT | G | 11 | a0001c0001t0001g0109 a0001c0001t0001g0131 a0001c0001t0001g0202 others(8): Show |
12 | HG00741.hp2 HG01516.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.134-4801_134-4799d others(5): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660194 | GTTTT | G | 57 | a0001c0001t0001g0103 a0001c0001t0001g0113 a0001c0001t0001g0114 others(54): Show |
57 | HG00280.hp1 HG00544.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.134-4802_134-4799d others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660194 | GTTTTT | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
95 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.134-4803_134-4799d others(7): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660194 | GTTTTTT | G | 62 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(59): Show |
62 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.134-4804_134-4799d others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660194 | GTTTTTTT | G | 9 | a0001c0002t0003g0152 a0001c0002t0019g0217 a0002c0003t0003g0056 others(6): Show |
9 | HG01891.hp2 HG02165.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-4805_134-4799d others(9): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660194 | GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0007g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.134-4812_134-4799d others(16): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660194 | GTTTTTTT others(8): Show |
G | 7 | a0001c0001t0007g0045 a0001c0001t0007g0085 a0001c0001t0007g0086 others(4): Show |
7 | HG02809.hp2 HG02818.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-4813_134-4799d others(17): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660194 | GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0020g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.134-4814_134-4799d others(18): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660194 | GTTTTTTT others(11): Show |
G | 16 | a0001c0002t0004g0225 a0001c0002t0006g0030 a0001c0002t0006g0031 others(13): Show |
16 | HG00738.hp2 HG01192.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.134-4816_134-4799d others(20): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660194 | GTTTTTTT others(13): Show |
G | 2 | a0001c0002t0003g0037 a0001c0002t0003g0038 |
2 | HG01074.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.134-4818_134-4799d others(22): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660194 | ||||||
| chr13:26660413 | A | G | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
95 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.134-4615A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26660413 | |||||||
| chr13:26660469 | G | C | 13 | a0001c0002t0006g0030 a0001c0002t0006g0031 a0001c0002t0006g0032 others(10): Show |
13 | HG01192.hp1 HG02148.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.134-4559G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26660469 | |||||||
| chr13:26660565 | G | C | 16 | a0001c0002t0003g0152 a0002c0003t0003g0048 a0002c0003t0003g0049 others(13): Show |
16 | HG00423.hp1 HG01069.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.134-4463G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26660565 | |||||||
| chr13:26660581 | G | GTA | 4 | a0001c0001t0001g0122 a0001c0001t0001g0142 a0002c0003t0003g0063 others(1): Show |
4 | HG00735.hp1 HG01123.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-4446_134-4445d others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26660581 | ||||||
| chr13:26660704 | A | T | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-4324A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26660704 | |||||||
| chr13:26660951 | G | A | 23 | a0001c0002t0004g0021 a0001c0002t0004g0022 a0001c0002t0004g0223 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.134-4077G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26660951 | |||||||
| chr13:26661282 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.134-3746C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26661282 | |||||||
| chr13:26661315 | C | T | 33 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(30): Show |
33 | HG00423.hp1 HG00738.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.134-3713C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26661315 | |||||||
| chr13:26661355 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.134-3673G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26661355 | |||||||
| chr13:26661484 | G | A | 23 | a0001c0002t0004g0021 a0001c0002t0004g0022 a0001c0002t0004g0223 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.134-3544G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26661484 | |||||||
| chr13:26661671 | G | A | 3 | a0002c0003t0011g0011 a0002c0003t0011g0012 a0002c0003t0011g0013 |
3 | HG02109.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.134-3357G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26661671 | |||||||
| chr13:26661758 | C | T | 1 | a0001c0001t0020g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.134-3270C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26661758 | |||||||
| chr13:26661882 | A | G | 62 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(59): Show |
62 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.134-3146A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26661882 | |||||||
| chr13:26661926 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
95 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.134-3102C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26661926 | |||||||
| chr13:26662014 | G | A | 7 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0131 others(4): Show |
7 | HG02056.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-3014G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26662014 | |||||||
| chr13:26662107 | C | T | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.134-2921C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26662107 | |||||||
| chr13:26662437 | T | G | 1 | a0001c0001t0002g0058 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.134-2591T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26662437 | |||||||
| chr13:26662495 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.134-2533A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26662495 | |||||||
| chr13:26662602 | C | T | 29 | a0001c0002t0004g0021 a0001c0002t0004g0022 a0001c0002t0004g0223 others(26): Show |
29 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.134-2426C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26662602 | |||||||
| chr13:26662750 | A | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(284): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.134-2278A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26662750 | |||||||
| chr13:26662867 | TCATACA | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.134-2131_134-2126d others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26662867 | ||||||
| chr13:26662867 | TCATACAC others(17): Show |
T | 1 | a0001c0001t0001g0140 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.134-2149_134-2126d others(26): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26662867 | ||||||
| chr13:26662888 | T | C | 7 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0131 others(4): Show |
7 | HG02056.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-2140T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26662888 | |||||||
| chr13:26662933 | G | A | 33 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(30): Show |
33 | HG00423.hp1 HG00738.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.134-2095G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26662933 | |||||||
| chr13:26662995 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
95 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.134-2033G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26662995 | |||||||
| chr13:26662997 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(100): Show |
103 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.134-2031G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26662997 | |||||||
| chr13:26663187 | T | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(284): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.134-1841T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26663187 | |||||||
| chr13:26663193 | T | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(284): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.134-1835T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26663193 | |||||||
| chr13:26663272 | C | T | 62 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(59): Show |
62 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.134-1756C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26663272 | |||||||
| chr13:26663296 | CTAGT | C | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.134-1728_134-1725d others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 26663296 | ||||||
| chr13:26663952 | A | G | 10 | a0001c0001t0002g0039 a0001c0001t0002g0042 a0001c0001t0002g0043 others(7): Show |
10 | HG00408.hp1 HG02015.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.134-1076A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26663952 | |||||||
| chr13:26664165 | A | G | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.134-863A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26664165 | |||||||
| chr13:26664255 | G | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(284): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.134-773G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26664255 | |||||||
| chr13:26664299 | G | A | 7 | a0001c0002t0006g0106 a0001c0002t0006g0107 a0001c0002t0006g0242 others(4): Show |
7 | HG01192.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-729G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26664299 | |||||||
| chr13:26664338 | T | C | 74 | a0001c0001t0008g0019 a0001c0002t0003g0037 a0001c0002t0003g0038 others(71): Show |
74 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.134-690T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26664338 | |||||||
| chr13:26664429 | G | A | 8 | a0001c0001t0007g0044 a0001c0001t0007g0045 a0001c0001t0007g0085 others(5): Show |
8 | HG02809.hp2 HG02818.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-599G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26664429 | |||||||
| chr13:26664435 | A | G | 2 | a0001c0001t0007g0044 a0001c0001t0007g0045 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.134-593A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26664435 | |||||||
| chr13:26664447 | C | G | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0061 others(1): Show |
4 | NA18940.hp1 NA18944.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-581C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26664447 | |||||||
| chr13:26664471 | G | A | 1 | a0002c0003t0003g0089 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.134-557G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26664471 | |||||||
| chr13:26664746 | C | T | 1 | a0001c0002t0026g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.134-282C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26664746 | |||||||
| chr13:26664934 | A | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0121 a0001c0001t0029g0157 |
3 | HG00673.hp1 NA18941.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.134-94A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26664934 | |||||||
| chr13:26665024 | A | G | 62 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(59): Show |
62 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(59): Show |
splice_region_variant&intron_variant | LOW | c.134-4A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 3/9 | chr13 | 26665024 | |||||||
| chr13:26665241 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0015g0015 a0001c0001t0015g0017 |
3 | HG01109.hp2 HG02145.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.268+79T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26665241 | |||||||
| chr13:26665304 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+142A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26665304 | |||||||
| chr13:26665549 | G | A | 1 | a0001c0001t0010g0162 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.268+387G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26665549 | |||||||
| chr13:26665587 | T | TA | 114 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(111): Show |
114 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.268+429dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 26665587 | ||||||
| chr13:26665676 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0169 |
3 | HG01891.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.268+514A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26665676 | |||||||
| chr13:26665840 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.268+678T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26665840 | |||||||
| chr13:26665850 | G | C | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.268+688G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26665850 | |||||||
| chr13:26665945 | T | G | 1 | a0001c0001t0001g0127 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.268+783T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26665945 | |||||||
| chr13:26666124 | C | A | 62 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(59): Show |
62 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.268+962C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26666124 | |||||||
| chr13:26666276 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.268+1114C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26666276 | |||||||
| chr13:26666408 | G | T | 4 | a0001c0001t0005g0264 a0001c0001t0005g0268 a0001c0001t0005g0269 others(1): Show |
4 | HG01081.hp2 HG01169.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-1109G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26666408 | |||||||
| chr13:26666463 | C | T | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.269-1054C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26666463 | |||||||
| chr13:26666565 | GT | G | 4 | a0001c0002t0009g0205 a0001c0002t0009g0208 a0001c0002t0009g0209 others(1): Show |
4 | HG02145.hp1 HG03195.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.269-950delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 26666565 | ||||||
| chr13:26666591 | A | G | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.269-926A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26666591 | |||||||
| chr13:26666665 | C | T | 3 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 |
3 | HG02622.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.269-852C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26666665 | |||||||
| chr13:26666666 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.269-851G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26666666 | |||||||
| chr13:26666671 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(115): Show |
118 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.269-846A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26666671 | |||||||
| chr13:26666696 | A | G | 8 | a0001c0001t0007g0044 a0001c0001t0007g0045 a0001c0001t0007g0085 others(5): Show |
8 | HG02809.hp2 HG02818.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.269-821A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26666696 | |||||||
| chr13:26666714 | A | G | 1 | a0003c0005t0008g0252 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.269-803A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26666714 | |||||||
| chr13:26666756 | G | A | 1 | a0001c0002t0009g0209 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.269-761G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26666756 | |||||||
| chr13:26666849 | A | G | 62 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(59): Show |
62 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.269-668A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26666849 | |||||||
| chr13:26666866 | C | CA | 12 | a0001c0001t0001g0149 a0001c0001t0001g0188 a0001c0001t0002g0275 others(9): Show |
12 | HG01175.hp2 HG02027.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.269-627dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 26666866 | ||||||
| chr13:26666866 | C | CAA | 55 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(52): Show |
55 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.269-628_269-627dup others(2): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 26666866 | ||||||
| chr13:26666866 | CA | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0129 a0001c0001t0001g0130 others(28): Show |
31 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.269-627delA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 26666866 | ||||||
| chr13:26666866 | CAAAAAAA others(1): Show |
C | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.269-634_269-627del others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 26666866 | ||||||
| chr13:26666952 | C | T | 1 | a0001c0001t0005g0267 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.269-565C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26666952 | |||||||
| chr13:26667080 | A | G | 12 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.269-437A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26667080 | |||||||
| chr13:26667320 | C | A | 1 | a0001c0002t0006g0106 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.269-197C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26667320 | |||||||
| chr13:26667428 | T | A | 3 | a0001c0002t0006g0030 a0001c0002t0006g0031 a0001c0002t0006g0032 |
3 | HG02148.hp1 HG02486.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.269-89T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26667428 | |||||||
| chr13:26667438 | T | G | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.269-79T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 4/9 | chr13 | 26667438 | |||||||
| chr13:26667867 | C | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(284): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.422+197C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26667867 | |||||||
| chr13:26667881 | A | G | 2 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
2 | NA19090.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.422+211A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26667881 | |||||||
| chr13:26667905 | G | A | 1 | a0001c0001t0037g0292 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.422+235G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26667905 | |||||||
| chr13:26667945 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.422+275T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26667945 | |||||||
| chr13:26668089 | GA | G | 35 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(32): Show |
35 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.422+426delA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 26668089 | ||||||
| chr13:26668246 | GACTA | G | 3 | a0001c0002t0009g0205 a0001c0002t0009g0208 a0001c0002t0025g0206 |
3 | HG02145.hp1 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.422+582_422+585del others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 26668246 | ||||||
| chr13:26668314 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.422+644C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26668314 | |||||||
| chr13:26668367 | C | T | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+697C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26668367 | |||||||
| chr13:26668401 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.422+731A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26668401 | |||||||
| chr13:26668443 | G | A | 1 | a0001c0001t0005g0259 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.422+773G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26668443 | |||||||
| chr13:26668494 | T | C | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.422+824T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26668494 | |||||||
| chr13:26668496 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.422+826C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26668496 | |||||||
| chr13:26668511 | A | G | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+841A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26668511 | |||||||
| chr13:26668520 | C | G | 40 | a0001c0001t0008g0019 a0001c0002t0004g0021 a0001c0002t0004g0022 others(37): Show |
40 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.422+850C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26668520 | |||||||
| chr13:26668614 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.422+944T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26668614 | |||||||
| chr13:26668715 | C | T | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.422+1045C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26668715 | |||||||
| chr13:26668904 | A | G | 88 | a0001c0001t0002g0002 a0001c0001t0002g0024 a0001c0001t0002g0028 others(85): Show |
89 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.422+1234A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26668904 | |||||||
| chr13:26669038 | A | G | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+1368A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26669038 | |||||||
| chr13:26669091 | T | TATTTGTA others(24): Show |
2 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
2 | NA19090.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.422+1422_422+1452d others(33): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 26669091 | ||||||
| chr13:26669136 | G | T | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.422+1466G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26669136 | |||||||
| chr13:26669206 | CT | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(249): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.422+1559delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 26669206 | ||||||
| chr13:26669206 | CTT | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(20): Show |
23 | HG00639.hp2 HG01069.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.422+1558_422+1559d others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 26669206 | ||||||
| chr13:26669213 | T | C | 8 | a0001c0001t0007g0044 a0001c0001t0007g0045 a0001c0001t0007g0085 others(5): Show |
8 | HG02809.hp2 HG02818.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.422+1543T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26669213 | |||||||
| chr13:26669249 | T | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(107): Show |
110 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.422+1579T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26669249 | |||||||
| chr13:26669250 | C | T | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.422+1580C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26669250 | |||||||
| chr13:26669338 | A | AG | 75 | a0001c0001t0008g0019 a0001c0002t0003g0037 a0001c0002t0003g0038 others(72): Show |
75 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.422+1668_422+1669i others(3): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26669338 | |||||||
| chr13:26669465 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0171 a0001c0001t0010g0182 |
3 | NA18951.hp1 NA18960.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.422+1795T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26669465 | |||||||
| chr13:26669514 | AT | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.422+1855delT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 26669514 | ||||||
| chr13:26669516 | T | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.422+1846T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26669516 | |||||||
| chr13:26669530 | C | T | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+1860C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26669530 | |||||||
| chr13:26669575 | G | A | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.422+1905G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26669575 | |||||||
| chr13:26669615 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | NA18977.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.422+1945G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26669615 | |||||||
| chr13:26669706 | G | A | 1 | a0001c0001t0002g0290 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.422+2036G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26669706 | |||||||
| chr13:26669844 | C | CT | 64 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(61): Show |
64 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.423-2027dupT | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 26669844 | ||||||
| chr13:26669938 | G | C | 58 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.423-1934G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26669938 | |||||||
| chr13:26670031 | A | T | 2 | a0001c0002t0011g0215 a0001c0002t0011g0216 |
2 | HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.423-1841A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26670031 | |||||||
| chr13:26670064 | T | G | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.423-1808T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26670064 | |||||||
| chr13:26670080 | G | A | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.423-1792G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26670080 | |||||||
| chr13:26670225 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.423-1647A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26670225 | |||||||
| chr13:26670257 | C | G | 6 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.423-1615C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26670257 | |||||||
| chr13:26670271 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.423-1601A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26670271 | |||||||
| chr13:26670337 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.423-1535G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26670337 | |||||||
| chr13:26670438 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.423-1434T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26670438 | |||||||
| chr13:26670562 | G | A | 4 | a0001c0001t0002g0046 a0001c0001t0002g0198 a0001c0001t0002g0199 others(1): Show |
4 | HG01070.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-1310G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26670562 | |||||||
| chr13:26670570 | G | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.423-1302G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26670570 | |||||||
| chr13:26670675 | G | A | 2 | a0002c0003t0003g0063 a0002c0003t0003g0066 |
2 | HG00735.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.423-1197G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26670675 | |||||||
| chr13:26670708 | A | G | 64 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(61): Show |
64 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.423-1164A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26670708 | |||||||
| chr13:26670963 | CTGTT | C | 3 | a0001c0002t0011g0215 a0001c0002t0011g0216 a0001c0002t0019g0217 |
3 | HG02622.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.423-906_423-903del others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 26670963 | ||||||
| chr13:26671012 | C | G | 1 | a0001c0002t0011g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.423-860C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26671012 | |||||||
| chr13:26671114 | T | C | 18 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 others(15): Show |
18 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.423-758T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26671114 | |||||||
| chr13:26671329 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(115): Show |
118 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.423-543A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 5/9 | chr13 | 26671329 | |||||||
| chr13:26672079 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(111): Show |
114 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.540+90T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26672079 | |||||||
| chr13:26672124 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(109): Show |
112 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.540+135A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26672124 | |||||||
| chr13:26672341 | C | T | 80 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.540+352C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26672341 | |||||||
| chr13:26672554 | A | T | 1 | a0001c0002t0004g0231 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.540+565A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26672554 | |||||||
| chr13:26672559 | A | G | 29 | a0001c0002t0004g0021 a0001c0002t0004g0022 a0001c0002t0004g0223 others(26): Show |
29 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.540+570A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26672559 | |||||||
| chr13:26672653 | G | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+664G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26672653 | |||||||
| chr13:26672667 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+678A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26672667 | |||||||
| chr13:26672777 | G | C | 1 | a0001c0002t0030g0227 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.540+788G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26672777 | |||||||
| chr13:26672845 | C | T | 4 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0010g0220 others(1): Show |
4 | HG01099.hp2 HG02602.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+856C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26672845 | |||||||
| chr13:26672877 | A | AAC | 4 | a0001c0001t0002g0043 a0001c0001t0002g0053 a0001c0001t0002g0067 others(1): Show |
4 | NA18952.hp2 NA18969.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+890_540+891dup others(2): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26672877 | ||||||
| chr13:26672893 | T | C | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+904T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26672893 | |||||||
| chr13:26673166 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.540+1177G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26673166 | |||||||
| chr13:26673207 | A | G | 1 | a0001c0004t0024g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.540+1218A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26673207 | |||||||
| chr13:26673209 | G | T | 1 | a0001c0004t0024g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.540+1220G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26673209 | |||||||
| chr13:26673210 | A | T | 1 | a0001c0004t0024g0196 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.540+1221A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26673210 | |||||||
| chr13:26673341 | A | G | 6 | a0001c0002t0009g0003 a0001c0002t0009g0207 a0001c0002t0009g0211 others(3): Show |
6 | HG02055.hp1 HG03041.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+1352A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26673341 | |||||||
| chr13:26673405 | T | G | 1 | a0001c0001t0002g0281 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.540+1416T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26673405 | |||||||
| chr13:26673451 | C | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+1462C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26673451 | |||||||
| chr13:26673641 | A | G | 64 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(61): Show |
64 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.540+1652A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26673641 | |||||||
| chr13:26673715 | T | C | 1 | a0001c0002t0035g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.540+1726T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26673715 | |||||||
| chr13:26673733 | G | A | 64 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(61): Show |
64 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.540+1744G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26673733 | |||||||
| chr13:26673735 | C | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(194): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.540+1746C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26673735 | |||||||
| chr13:26673802 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.540+1813G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26673802 | |||||||
| chr13:26673996 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(12): Show |
15 | HG00639.hp2 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+2007C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26673996 | |||||||
| chr13:26674040 | T | C | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.540+2051T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26674040 | |||||||
| chr13:26674231 | C | T | 2 | a0001c0001t0008g0249 a0001c0001t0008g0250 |
2 | HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.540+2242C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26674231 | |||||||
| chr13:26674274 | G | A | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.541-2275G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26674274 | |||||||
| chr13:26674306 | C | G | 23 | a0001c0002t0004g0021 a0001c0002t0004g0022 a0001c0002t0004g0223 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.541-2243C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26674306 | |||||||
| chr13:26674785 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.541-1764T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26674785 | |||||||
| chr13:26674836 | C | T | 3 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0136 |
3 | HG01943.hp1 HG01975.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.541-1713C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26674836 | |||||||
| chr13:26674880 | G | A | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.541-1669G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26674880 | |||||||
| chr13:26674941 | C | T | 1 | a0001c0002t0009g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.541-1608C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26674941 | |||||||
| chr13:26674944 | A | G | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.541-1605A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26674944 | |||||||
| chr13:26674971 | T | C | 4 | a0002c0003t0003g0049 a0002c0003t0003g0050 a0002c0003t0003g0051 others(1): Show |
4 | HG00423.hp1 HG02080.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-1578T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26674971 | |||||||
| chr13:26674981 | A | G | 1 | a0001c0002t0031g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.541-1568A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26674981 | |||||||
| chr13:26675021 | G | T | 1 | a0001c0001t0020g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.541-1528G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26675021 | |||||||
| chr13:26675481 | T | TAC | 10 | a0001c0001t0008g0248 a0001c0001t0008g0249 a0001c0001t0008g0250 others(7): Show |
10 | HG02145.hp1 HG02257.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.541-1027_541-1026d others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675481 | ||||||
| chr13:26675481 | TAC | T | 42 | a0001c0001t0002g0024 a0001c0001t0002g0029 a0001c0001t0002g0039 others(39): Show |
42 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.541-1027_541-1026d others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675481 | ||||||
| chr13:26675481 | TACAC | T | 34 | a0001c0001t0002g0002 a0001c0001t0002g0071 a0001c0001t0002g0253 others(31): Show |
35 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.541-1029_541-1026d others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675481 | ||||||
| chr13:26675481 | TACACAC | T | 28 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0061 others(25): Show |
28 | HG00099.hp1 HG01069.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.541-1031_541-1026d others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675481 | ||||||
| chr13:26675481 | TACACACA others(1): Show |
T | 14 | a0001c0001t0001g0036 a0001c0001t0002g0283 a0001c0001t0002g0285 others(11): Show |
14 | HG00280.hp1 HG01081.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.541-1033_541-1026d others(10): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675481 | ||||||
| chr13:26675481 | TACACACA others(3): Show |
T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(26): Show |
29 | HG00639.hp2 HG00738.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.541-1035_541-1026d others(12): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675481 | ||||||
| chr13:26675481 | TACACACA others(5): Show |
T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0102 others(116): Show |
119 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.541-1037_541-1026d others(14): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675481 | ||||||
| chr13:26675481 | TACACACA others(7): Show |
T | 2 | a0001c0002t0003g0152 a0002c0003t0011g0011 |
2 | HG02109.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.541-1039_541-1026d others(16): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675481 | ||||||
| chr13:26675481 | TACACACA others(9): Show |
T | 5 | a0002c0003t0003g0098 a0002c0003t0003g0099 a0002c0003t0003g0201 others(2): Show |
5 | HG01891.hp2 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-1041_541-1026d others(18): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675481 | ||||||
| chr13:26675528 | A | G | 1 | a0001c0001t0002g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.541-1021A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26675528 | |||||||
| chr13:26675552 | G | A | 2 | a0001c0001t0001g0036 a0001c0004t0024g0196 |
2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.541-997G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26675552 | |||||||
| chr13:26675637 | A | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(284): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.541-912A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26675637 | |||||||
| chr13:26675650 | C | CTG | 114 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(111): Show |
114 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.541-877_541-876dup others(2): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675650 | ||||||
| chr13:26675650 | C | CTGTG | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(8): Show |
11 | HG00639.hp2 HG01255.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.541-879_541-876dup others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675650 | ||||||
| chr13:26675650 | C | CTGTGTGT others(7): Show |
7 | a0001c0002t0009g0003 a0001c0002t0009g0207 a0001c0002t0009g0211 others(4): Show |
7 | HG02055.hp1 HG02071.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.541-889_541-876dup others(14): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675650 | ||||||
| chr13:26675650 | C | CTGTGTGT others(9): Show |
3 | a0001c0002t0009g0205 a0001c0002t0009g0208 a0001c0002t0031g0214 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.541-891_541-876dup others(16): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675650 | ||||||
| chr13:26675650 | C | CTGTGTGT others(11): Show |
5 | a0001c0002t0004g0228 a0001c0002t0004g0231 a0001c0002t0004g0235 others(2): Show |
5 | HG00280.hp1 HG01074.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-893_541-876dup others(18): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675650 | ||||||
| chr13:26675650 | C | CTGTGTGT others(13): Show |
7 | a0001c0002t0003g0152 a0001c0002t0004g0234 a0001c0002t0011g0215 others(4): Show |
7 | HG01433.hp1 HG02622.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-895_541-876dup others(20): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675650 | ||||||
| chr13:26675650 | C | CTGTGTGT others(15): Show |
30 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0004g0223 others(27): Show |
30 | HG00099.hp1 HG00423.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.541-897_541-876dup others(22): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675650 | ||||||
| chr13:26675650 | C | CTGTGTGT others(17): Show |
9 | a0001c0002t0004g0225 a0001c0002t0006g0034 a0001c0002t0006g0242 others(6): Show |
9 | HG00738.hp2 HG01981.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-876_541-875ins others(24): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675650 | ||||||
| chr13:26675650 | C | CTGTGTGT others(19): Show |
5 | a0001c0002t0004g0021 a0001c0002t0006g0213 a0001c0002t0006g0244 others(2): Show |
5 | HG02717.hp1 HG03041.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-876_541-875ins others(26): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675650 | ||||||
| chr13:26675650 | C | CTGTGTGT others(21): Show |
1 | a0001c0002t0006g0030 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.541-876_541-875ins others(28): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675650 | ||||||
| chr13:26675650 | C | CTGTGTGT others(23): Show |
6 | a0001c0002t0004g0022 a0001c0002t0006g0031 a0001c0002t0006g0032 others(3): Show |
6 | HG01175.hp1 HG01243.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-876_541-875ins others(30): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 26675650 | ||||||
| chr13:26675673 | T | TGTGTGTG others(14): Show |
1 | a0002c0003t0011g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.541-876_541-875ins others(21): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26675673 | |||||||
| chr13:26675673 | T | TGTGTGTG others(22): Show |
1 | a0001c0002t0006g0107 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.541-876_541-875ins others(29): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26675673 | |||||||
| chr13:26675723 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(95): Show |
98 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.541-826A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26675723 | |||||||
| chr13:26675916 | A | G | 3 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 |
3 | HG02717.hp2 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.541-633A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26675916 | |||||||
| chr13:26675934 | G | C | 75 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(72): Show |
75 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.541-615G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26675934 | |||||||
| chr13:26675959 | C | A | 1 | a0001c0002t0006g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.541-590C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26675959 | |||||||
| chr13:26676186 | A | G | 1 | a0001c0002t0017g0229 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.541-363A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 6/9 | chr13 | 26676186 | |||||||
| chr13:26676808 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(99): Show |
102 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.716+84A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26676808 | |||||||
| chr13:26677234 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.716+510A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26677234 | |||||||
| chr13:26677465 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(95): Show |
98 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.716+741A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26677465 | |||||||
| chr13:26677589 | C | T | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.716+865C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26677589 | |||||||
| chr13:26677665 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.716+941G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26677665 | |||||||
| chr13:26677666 | T | C | 38 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(35): Show |
38 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.716+942T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26677666 | |||||||
| chr13:26677688 | A | T | 3 | a0001c0001t0002g0282 a0001c0001t0002g0286 a0001c0001t0002g0287 |
3 | NA18612.hp2 NA18944.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.716+964A>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26677688 | |||||||
| chr13:26677693 | A | C | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.716+969A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26677693 | |||||||
| chr13:26677796 | T | C | 1 | a0001c0001t0007g0086 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.716+1072T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26677796 | |||||||
| chr13:26677956 | T | G | 1 | a0001c0001t0002g0068 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.716+1232T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26677956 | |||||||
| chr13:26677979 | A | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0109 a0001c0001t0001g0111 others(44): Show |
47 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.716+1255A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26677979 | |||||||
| chr13:26677987 | G | GA | 21 | a0001c0002t0003g0152 a0002c0003t0003g0048 a0002c0003t0003g0049 others(18): Show |
21 | HG00423.hp1 HG00735.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.716+1264dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 26677987 | ||||||
| chr13:26678020 | T | C | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.716+1296T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26678020 | |||||||
| chr13:26678033 | G | T | 1 | a0001c0001t0008g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.716+1309G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26678033 | |||||||
| chr13:26678119 | ATTGT | A | 88 | a0001c0001t0002g0002 a0001c0001t0002g0024 a0001c0001t0002g0028 others(85): Show |
89 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.716+1398_716+1401d others(6): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 26678119 | ||||||
| chr13:26678698 | A | C | 74 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(71): Show |
74 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.716+1974A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26678698 | |||||||
| chr13:26679085 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.717-1969C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26679085 | |||||||
| chr13:26679092 | G | A | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.717-1962G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26679092 | |||||||
| chr13:26679122 | TC | T | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.717-1931delC | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26679122 | |||||||
| chr13:26679230 | C | T | 1 | a0001c0001t0005g0266 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.717-1824C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26679230 | |||||||
| chr13:26679249 | C | G | 4 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.717-1805C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26679249 | |||||||
| chr13:26679502 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.717-1552C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26679502 | |||||||
| chr13:26679542 | C | T | 1 | a0001c0002t0011g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.717-1512C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26679542 | |||||||
| chr13:26679966 | G | A | 1 | a0001c0002t0028g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.717-1088G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26679966 | |||||||
| chr13:26680074 | G | A | 1 | a0001c0002t0028g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.717-980G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26680074 | |||||||
| chr13:26680175 | C | T | 1 | a0001c0001t0005g0262 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.717-879C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26680175 | |||||||
| chr13:26680290 | A | G | 2 | a0001c0001t0005g0261 a0001c0001t0005g0262 |
2 | HG01255.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.717-764A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26680290 | |||||||
| chr13:26680386 | G | A | 1 | a0001c0002t0004g0235 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.717-668G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26680386 | |||||||
| chr13:26680540 | TTTG | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0121 a0001c0001t0029g0157 |
3 | HG00673.hp1 NA18941.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.717-511_717-509del others(3): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 26680540 | ||||||
| chr13:26680754 | C | T | 1 | a0001c0001t0023g0094 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.717-300C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26680754 | |||||||
| chr13:26680875 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.717-179T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 7/9 | chr13 | 26680875 | |||||||
| chr13:26681394 | T | G | 1 | a0001c0001t0005g0267 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.983+74T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26681394 | |||||||
| chr13:26681413 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.983+93A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26681413 | |||||||
| chr13:26681559 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.983+239T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26681559 | |||||||
| chr13:26681894 | G | T | 4 | a0001c0004t0013g0033 a0001c0004t0013g0195 a0001c0004t0013g0197 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.983+574G>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26681894 | |||||||
| chr13:26681930 | C | T | 17 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0006g0030 others(14): Show |
17 | HG00738.hp2 HG01074.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.983+610C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26681930 | |||||||
| chr13:26681941 | T | C | 23 | a0001c0002t0004g0021 a0001c0002t0004g0022 a0001c0002t0004g0223 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.983+621T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26681941 | |||||||
| chr13:26681945 | C | T | 1 | a0001c0001t0020g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.983+625C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26681945 | |||||||
| chr13:26681957 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.983+637G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26681957 | |||||||
| chr13:26681965 | A | G | 74 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(71): Show |
74 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.984-642A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26681965 | |||||||
| chr13:26681985 | A | G | 64 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(61): Show |
64 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.984-622A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26681985 | |||||||
| chr13:26682023 | C | A | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0184 |
3 | HG01109.hp1 HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.984-584C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26682023 | |||||||
| chr13:26682229 | T | C | 1 | a0001c0002t0016g0010 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.984-378T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26682229 | |||||||
| chr13:26682311 | G | A | 2 | a0001c0001t0008g0249 a0001c0001t0008g0250 |
2 | HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.984-296G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26682311 | |||||||
| chr13:26682490 | A | G | 1 | a0001c0001t0014g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.984-117A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26682490 | |||||||
| chr13:26682550 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.984-57C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26682550 | |||||||
| chr13:26682591 | C | G | 64 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(61): Show |
64 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.984-16C>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26682591 | |||||||
| chr13:26682593 | C | A | 1 | a0001c0001t0020g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.984-14C>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 8/9 | chr13 | 26682593 | |||||||
| chr13:26683071 | A | G | 1 | a0001c0001t0002g0290 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1351+97A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26683071 | |||||||
| chr13:26683199 | G | A | 7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0119 others(4): Show |
7 | HG02027.hp1 HG02083.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.1351+225G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26683199 | |||||||
| chr13:26683245 | T | G | 82 | a0001c0001t0007g0044 a0001c0001t0007g0045 a0001c0001t0007g0085 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1351+271T>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26683245 | |||||||
| chr13:26683261 | C | T | 2 | a0001c0001t0010g0220 a0001c0001t0010g0221 |
2 | HG02602.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1351+287C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26683261 | |||||||
| chr13:26683474 | C | CA | 58 | a0001c0001t0001g0001 a0001c0001t0001g0109 a0001c0001t0001g0111 others(55): Show |
58 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1351+513dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 26683474 | ||||||
| chr13:26683488 | GAATTGA | G | 64 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0152 others(61): Show |
64 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1351+519_1351+524d others(8): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 26683488 | ||||||
| chr13:26683551 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
118 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1351+577T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26683551 | |||||||
| chr13:26683636 | T | TA | 11 | a0001c0001t0008g0019 a0001c0002t0009g0003 a0001c0002t0009g0205 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.1351+674dupA | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 26683636 | ||||||
| chr13:26683675 | G | A | 2 | a0003c0005t0008g0251 a0003c0005t0008g0252 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1351+701G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26683675 | |||||||
| chr13:26683710 | A | G | 1 | a0001c0002t0016g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1351+736A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26683710 | |||||||
| chr13:26683751 | C | T | 1 | a0001c0001t0005g0266 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1351+777C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26683751 | |||||||
| chr13:26683949 | C | T | 21 | a0001c0002t0003g0152 a0002c0003t0003g0048 a0002c0003t0003g0049 others(18): Show |
21 | HG00423.hp1 HG00735.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.1351+975C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26683949 | |||||||
| chr13:26683959 | G | C | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1351+985G>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26683959 | |||||||
| chr13:26684119 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(102): Show |
105 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1351+1145A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26684119 | |||||||
| chr13:26684327 | T | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(284): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1351+1353T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26684327 | |||||||
| chr13:26684470 | A | AC | 197 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(194): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1352-1218_1352-121 others(5): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26684470 | |||||||
| chr13:26684487 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1352-1201C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26684487 | |||||||
| chr13:26684514 | A | C | 5 | a0001c0001t0001g0036 a0001c0004t0013g0033 a0001c0004t0013g0195 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1352-1174A>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26684514 | |||||||
| chr13:26684585 | A | G | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1352-1103A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26684585 | |||||||
| chr13:26684641 | C | CG | 19 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0125 others(16): Show |
19 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1352-1042dupG | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 26684641 | ||||||
| chr13:26684703 | A | G | 1 | a0001c0001t0010g0182 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1352-985A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26684703 | |||||||
| chr13:26684860 | A | G | 10 | a0001c0002t0009g0003 a0001c0002t0009g0205 a0001c0002t0009g0207 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1352-828A>G | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26684860 | |||||||
| chr13:26684883 | T | A | 1 | a0001c0002t0006g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1352-805T>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26684883 | |||||||
| chr13:26684888 | T | C | 1 | a0001c0002t0016g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1352-800T>C | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26684888 | |||||||
| chr13:26685034 | GCCATGAT others(4): Show |
G | 1 | a0001c0001t0034g0203 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1352-653_1352-643d others(13): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26685034 | |||||||
| chr13:26685087 | CAA | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(190): Show |
193 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1352-585_1352-584d others(4): Show |
WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 26685087 | ||||||
| chr13:26685238 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1352-450G>A | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26685238 | |||||||
| chr13:26685672 | C | T | 6 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG02056.hp1 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1352-16C>T | WASF3 | ENSG00000132970.14 | transcript | ENST00000335327.6 | protein_coding | 9/9 | chr13 | 26685672 |