Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10254 |
| ensemblid | ENSG00000115145.10 |
| hgncid | 11358 |
| symbol | STAM2 |
| name | signal transducing adaptor molecule 2 |
| refseq_nuc | NM_005843.6 |
| refseq_prot | NP_005834.4 |
| ensembl_nuc | ENST00000263904.5 |
| ensembl_prot | ENSP00000263904.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 152116801 |
| end | 152175763 |
| strand | - |
| ver | v1.2 |
| region | chr2:152116801-152175763 |
| region5000 | chr2:152111801-152180763 |
| regionname0 | STAM2_chr2_152116801_152175763 |
| regionname5000 | STAM2_chr2_152111801_152180763 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 525 | 358 | 90 | 64 | 144 | 14 | 44 | 112 | STAM2_chr2_152111801_152180763 | STAM2 | MPLFT others(520): Show |
chr2 | 152111801 | 152180763 |
| a0002 | 0/0 | 525 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | MPLFT others(520): Show |
chr2 | 152111801 | 152180763 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1575 | 354 | 86 | 64 | 144 | 14 | 44 | STAM2_chr2_152111801_152180763 | STAM2 | ATGCC others(1570): Show |
chr2 | 152111801 | 152180763 | ||
| a0001c0002 | 0/0 | 1575 | 3 | 3 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | ATGCC others(1570): Show |
chr2 | 152111801 | 152180763 | ||
| a0001c0004 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | ATGCC others(1570): Show |
chr2 | 152111801 | 152180763 | ||
| a0002c0003 | 0/0 | 1575 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | ATGCC others(1570): Show |
chr2 | 152111801 | 152180763 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5472 | 61 | 6 | 22 | 20 | 5 | 7 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0002 | 0/0 | 5471 | 42 | 1 | 0 | 30 | 0 | 11 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5466): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0003 | 0/0 | 5477 | 32 | 2 | 4 | 15 | 1 | 10 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5472): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0004 | 0/0 | 5475 | 27 | 3 | 10 | 12 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5470): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0005 | 0/0 | 5470 | 21 | 0 | 1 | 18 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5465): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0006 | 0/0 | 5471 | 21 | 5 | 7 | 5 | 3 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5466): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0007 | 0/0 | 5472 | 14 | 14 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0008 | 0/0 | 5472 | 13 | 1 | 3 | 7 | 1 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0009 | 0/0 | 5472 | 11 | 10 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0010 | 0/0 | 5472 | 7 | 0 | 0 | 7 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0011 | 0/0 | 5471 | 7 | 6 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5466): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0012 | 0/0 | 5474 | 7 | 6 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5469): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0013 | 0/0 | 5472 | 6 | 0 | 4 | 0 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0014 | 0/0 | 5475 | 6 | 5 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5470): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0015 | 0/0 | 5473 | 6 | 3 | 0 | 1 | 1 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5468): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0016 | 0/0 | 5472 | 5 | 5 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0017 | 0/0 | 5473 | 5 | 0 | 0 | 5 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5468): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0019 | 0/0 | 5474 | 4 | 0 | 1 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5469): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0020 | 0/0 | 5478 | 4 | 4 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5473): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0021 | 0/0 | 5480 | 4 | 3 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5475): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0022 | 0/0 | 5478 | 4 | 0 | 0 | 3 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5473): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0023 | 0/0 | 5474 | 4 | 0 | 3 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5469): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0024 | 0/0 | 5479 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5474): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0025 | 0/0 | 5473 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5468): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0026 | 0/0 | 5472 | 2 | 0 | 0 | 0 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0027 | 0/0 | 5476 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5471): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0028 | 0/0 | 5472 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0029 | 0/0 | 5471 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5466): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0030 | 0/0 | 5470 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5465): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0031 | 0/0 | 5470 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5465): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0032 | 0/0 | 5471 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5466): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0033 | 0/0 | 5471 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5466): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0034 | 0/0 | 5471 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5466): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0035 | 0/0 | 5475 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5470): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0036 | 0/0 | 5472 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0037 | 0/0 | 5475 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5470): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0038 | 0/0 | 5472 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0039 | 0/0 | 5472 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0040 | 0/0 | 5472 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0041 | 0/0 | 5472 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0042 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5471): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0043 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5471): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0044 | 0/0 | 5471 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5466): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0045 | 0/0 | 5473 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5468): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0046 | 0/0 | 5473 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5468): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0047 | 0/0 | 5475 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5470): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0048 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5472): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0049 | 0/1 | 5477 | 1 | 0 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5472): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0050 | 0/0 | 5474 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5469): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0051 | 0/0 | 5474 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5469): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0052 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5471): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0053 | 0/0 | 5473 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5468): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0054 | 0/0 | 5475 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5470): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0055 | 0/0 | 5473 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5468): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0056 | 0/0 | 5473 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5468): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0057 | 0/0 | 5475 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5470): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0058 | 0/0 | 5471 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5466): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0059 | 0/0 | 5474 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5469): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0060 | 0/0 | 5473 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5468): Show |
chr2 | 152111801 | 152180763 |
| a0001c0001t0061 | 0/0 | 5471 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | CAGTG others(5466): Show |
chr2 | 152111801 | 152180763 |
| a0001c0002t0018 | 0/0 | 5475 | 3 | 3 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5470): Show |
chr2 | 152111801 | 152180763 |
| a0001c0004t0018 | 0/0 | 5475 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5470): Show |
chr2 | 152111801 | 152180763 |
| a0002c0003t0001 | 0/0 | 5472 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5467): Show |
chr2 | 152111801 | 152180763 |
| a0002c0003t0003 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | AAGTG others(5472): Show |
chr2 | 152111801 | 152180763 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0006g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0007g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0008g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0008g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0008g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0008g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0008g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0008g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0008g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0008g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0008g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0008g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0008g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0009g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0009g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0010g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0010g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0010g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0010g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0010g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0010g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0011g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0011g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0011g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0011g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0011g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0011g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0012g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0012g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0012g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0012g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0012g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0013g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0013g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0013g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0013g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0013g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0014g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0014g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0014g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0014g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0015g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0015g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0015g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0015g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0015g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0015g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0016g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0016g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0016g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0016g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0016g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0017g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0017g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0017g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0017g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0017g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0019g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0019g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0019g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0019g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0020g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0020g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0020g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0020g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0021g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0021g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0021g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0021g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0022g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0022g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0022g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0022g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0023g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0023g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0023g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0023g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0024g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0024g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0024g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0025g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0025g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0026g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0027g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0027g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0028g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0029g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0030g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0031g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0032g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0033g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0034g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0035g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0036g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0037g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0038g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0039g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0040g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0041g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0042g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0043g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0044g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0045g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0046g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0047g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0048g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0049g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0050g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0051g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0052g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0053g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0054g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0055g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0056g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0057g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0058g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0059g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0060g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0001t0061g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0002t0018g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0002t0018g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0002t0018g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0001c0004t0018g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0002c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| a0002c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0217 | EUR | GBR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0292 | EUR | GBR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0175 | EUR | GBR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00280 | hp1 | a0001 | c0001 | t0032 | g0103 | EUR | FIN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00280 | hp2 | a0001 | c0001 | t0015 | g0285 | EUR | FIN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00408 | hp2 | a0001 | c0001 | t0017 | g0219 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00609 | hp1 | a0001 | c0001 | t0022 | g0232 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00639 | hp1 | a0001 | c0001 | t0012 | g0167 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00639 | hp2 | a0001 | c0001 | t0021 | g0169 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00673 | hp2 | a0001 | c0001 | t0015 | g0283 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0215 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01070 | hp1 | a0001 | c0001 | t0019 | g0198 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01070 | hp2 | a0001 | c0001 | t0027 | g0162 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01074 | hp1 | a0001 | c0001 | t0013 | g0295 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0306 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0303 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0134 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0307 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01109 | hp2 | a0001 | c0001 | t0057 | g0187 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0135 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01167 | hp2 | a0001 | c0001 | t0014 | g0036 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0129 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0130 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01192 | hp1 | a0001 | c0001 | t0013 | g0253 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01192 | hp2 | a0001 | c0001 | t0011 | g0141 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01256 | hp1 | a0001 | c0001 | t0013 | g0025 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01256 | hp2 | a0001 | c0001 | t0023 | g0210 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0213 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01258 | hp2 | a0001 | c0001 | t0013 | g0025 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01261 | hp1 | a0001 | c0001 | t0008 | g0308 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0302 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0236 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01496 | hp2 | a0001 | c0001 | t0027 | g0158 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0148 | EUR | IBS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01517 | hp1 | a0001 | c0001 | t0045 | g0244 | EUR | IBS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0147 | EUR | IBS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0114 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0117 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01891 | hp2 | a0001 | c0001 | t0020 | g0173 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0206 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0193 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01978 | hp1 | a0001 | c0001 | t0047 | g0199 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0080 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01981 | hp2 | a0001 | c0001 | t0023 | g0192 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02015 | hp1 | a0002 | c0003 | t0003 | g0227 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0068 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02027 | hp1 | a0001 | c0001 | t0038 | g0092 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02027 | hp2 | a0001 | c0001 | t0058 | g0304 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02040 | hp1 | a0001 | c0001 | t0019 | g0190 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02040 | hp2 | a0001 | c0001 | t0041 | g0286 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02055 | hp1 | a0001 | c0001 | t0015 | g0287 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02055 | hp2 | a0001 | c0001 | t0015 | g0111 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02056 | hp2 | a0001 | c0001 | t0017 | g0216 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02080 | hp1 | a0001 | c0001 | t0039 | g0281 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0133 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0050 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02145 | hp2 | a0001 | c0001 | t0044 | g0180 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02148 | hp2 | a0001 | c0001 | t0023 | g0205 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | CDX | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CDX | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02165 | hp1 | a0001 | c0001 | t0022 | g0230 | EAS | CDX | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CDX | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02257 | hp1 | a0001 | c0001 | t0033 | g0109 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02257 | hp2 | a0001 | c0001 | t0021 | g0172 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02258 | hp1 | a0001 | c0001 | t0020 | g0155 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0122 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0145 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0212 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02300 | hp1 | a0001 | c0001 | t0029 | g0136 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0165 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0040 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02622 | hp1 | a0001 | c0001 | t0042 | g0161 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02622 | hp2 | a0001 | c0001 | t0016 | g0029 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02630 | hp1 | a0001 | c0001 | t0021 | g0168 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0143 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02647 | hp2 | a0001 | c0001 | t0051 | g0095 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02683 | hp1 | a0001 | c0001 | t0013 | g0290 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0178 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0102 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0124 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0160 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0119 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02738 | hp2 | a0001 | c0001 | t0022 | g0243 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0038 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0142 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0299 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02886 | hp1 | a0001 | c0001 | t0054 | g0152 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0043 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02895 | hp1 | a0001 | c0001 | t0012 | g0163 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0300 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02896 | hp2 | a0001 | c0001 | t0014 | g0033 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0164 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02922 | hp1 | a0001 | c0001 | t0056 | g0049 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0297 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02965 | hp1 | a0001 | c0001 | t0011 | g0140 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02976 | hp1 | a0001 | c0004 | t0018 | g0174 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03041 | hp1 | a0001 | c0001 | t0052 | g0096 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03041 | hp2 | a0001 | c0001 | t0012 | g0159 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03098 | hp2 | a0001 | c0001 | t0016 | g0028 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03130 | hp1 | a0001 | c0001 | t0021 | g0171 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03139 | hp2 | a0001 | c0001 | t0043 | g0157 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03195 | hp1 | a0001 | c0001 | t0046 | g0176 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03195 | hp2 | a0001 | c0002 | t0018 | g0151 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03209 | hp1 | a0001 | c0001 | t0020 | g0156 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0121 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03225 | hp1 | a0001 | c0001 | t0016 | g0106 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0118 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0247 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03239 | hp2 | a0001 | c0001 | t0026 | g0022 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0123 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0298 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0301 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0115 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03540 | hp1 | a0001 | c0002 | t0018 | g0153 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0131 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03688 | hp1 | a0001 | c0001 | t0060 | g0312 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0246 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03710 | hp2 | a0001 | c0001 | t0013 | g0291 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0248 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0311 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03834 | hp1 | a0001 | c0001 | t0035 | g0077 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0191 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0218 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03927 | hp2 | a0001 | c0001 | t0034 | g0064 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0188 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0252 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG04115 | hp2 | a0001 | c0001 | t0015 | g0275 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0030 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG04228 | hp1 | a0001 | c0001 | t0026 | g0022 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0042 | AFR | YRI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0166 | AFR | YRI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0270 | EAS | CHB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | CHB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0044 | AFR | YRI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18906 | hp2 | a0001 | c0001 | t0016 | g0105 | AFR | YRI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18941 | hp1 | a0001 | c0001 | t0059 | g0314 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18942 | hp2 | a0001 | c0001 | t0008 | g0305 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18943 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18948 | hp1 | a0001 | c0001 | t0010 | g0108 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18950 | hp2 | a0001 | c0001 | t0024 | g0189 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18952 | hp1 | a0001 | c0001 | t0024 | g0225 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18952 | hp2 | a0001 | c0001 | t0010 | g0011 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0149 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18963 | hp1 | a0001 | c0001 | t0019 | g0194 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18968 | hp1 | a0001 | c0001 | t0008 | g0309 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18968 | hp2 | a0001 | c0001 | t0022 | g0241 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18969 | hp2 | a0001 | c0001 | t0008 | g0317 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18970 | hp2 | a0001 | c0001 | t0061 | g0128 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18973 | hp1 | a0001 | c0001 | t0024 | g0233 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18982 | hp1 | a0001 | c0001 | t0010 | g0082 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18983 | hp1 | a0001 | c0001 | t0017 | g0202 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18986 | hp1 | a0001 | c0001 | t0050 | g0081 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18986 | hp2 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18994 | hp1 | a0001 | c0001 | t0010 | g0083 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18994 | hp2 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19006 | hp1 | a0001 | c0001 | t0031 | g0069 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19006 | hp2 | a0001 | c0001 | t0023 | g0208 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19009 | hp1 | a0001 | c0001 | t0048 | g0238 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19043 | hp1 | a0001 | c0001 | t0028 | g0037 | AFR | LWK | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19043 | hp2 | a0001 | c0001 | t0020 | g0170 | AFR | LWK | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19055 | hp1 | a0001 | c0001 | t0010 | g0056 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19060 | hp1 | a0001 | c0001 | t0008 | g0313 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19064 | hp2 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19067 | hp1 | a0001 | c0001 | t0010 | g0063 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0127 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0139 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19075 | hp1 | a0001 | c0001 | t0008 | g0315 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19075 | hp2 | a0001 | c0001 | t0025 | g0099 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19079 | hp2 | a0001 | c0001 | t0019 | g0214 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19084 | hp1 | a0001 | c0001 | t0025 | g0085 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19086 | hp1 | a0001 | c0001 | t0036 | g0209 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19086 | hp2 | a0001 | c0001 | t0030 | g0057 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19088 | hp1 | a0001 | c0001 | t0017 | g0196 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19088 | hp2 | a0001 | c0001 | t0010 | g0011 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19089 | hp1 | a0001 | c0001 | t0037 | g0197 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19090 | hp1 | a0001 | c0001 | t0017 | g0220 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0144 | AFR | YRI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0047 | AFR | YRI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA20129 | hp1 | a0001 | c0001 | t0053 | g0125 | AFR | ASW | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0316 | AFR | ASW | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA20752 | hp1 | a0001 | c0001 | t0040 | g0280 | EUR | TSI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0266 | EUR | TSI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0310 | EUR | TSI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0026 | SAS | GIH | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0138 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0120 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02109 | hp2 | a0001 | c0001 | t0014 | g0031 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02486 | hp1 | a0001 | c0001 | t0015 | g0112 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02486 | hp2 | a0001 | c0001 | t0016 | g0104 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02559 | hp1 | a0001 | c0002 | t0018 | g0154 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG02559 | hp2 | a0001 | c0001 | t0014 | g0035 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0146 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG06807 | hp1 | a0001 | c0001 | t0014 | g0032 | AFR | USA | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0041 | AFR | USA | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA20300 | hp1 | a0001 | c0001 | t0055 | g0116 | AFR | USA | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0045 | AFR | USA | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA21309 | hp1 | a0001 | c0001 | t0014 | g0034 | AFR | LWK | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | LWK | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0049 | g0177 | REF | REF | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0110 | REF | REF | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:152116803 | C | T | 1 | a0001 | 1 | HG01517.hp1 | splice_region_variant | LOW | c.*3771G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | chr2 | 152116803 | |||||||
| chr2:152148043 | C | T | 1 | a0002 | 2 | HG02015.hp1 NA18747.hp1 |
missense_variant | MODERATE | c.281G>A | p.Arg94His | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/14 | 402/5472 | 281/1578 | 94/525 | chr2 | 152148043 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:152123849 | G | A | 2 | a0001c0002 a0001c0004 |
4 | HG02559.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.1266C>T | p.Pro422Pro | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/14 | 1387/5472 | 1266/1578 | 422/525 | chr2 | 152123849 | |||
| chr2:152123876 | A | G | 1 | a0001c0004 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1239T>C | p.Thr413Thr | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/14 | 1360/5472 | 1239/1578 | 413/525 | chr2 | 152123876 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:152117109 | T | C | 4 | a0001c0001t0008 a0001c0001t0038 a0001c0001t0059 others(1): Show |
16 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3465A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 3465 | chr2 | 152117109 | ||||||
| chr2:152117596 | G | C | 1 | a0001c0001t0014 | 6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2978C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2978 | chr2 | 152117596 | ||||||
| chr2:152117656 | C | T | 1 | a0001c0001t0013 | 6 | HG01074.hp1 HG01192.hp1 HG01256.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2918G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2918 | chr2 | 152117656 | ||||||
| chr2:152117740 | A | T | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(14): Show |
88 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2834T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2834 | chr2 | 152117740 | ||||||
| chr2:152117952 | T | G | 1 | a0001c0001t0027 | 2 | HG01070.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2622A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2622 | chr2 | 152117952 | ||||||
| chr2:152118008 | C | T | 1 | a0001c0001t0040 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2566G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2566 | chr2 | 152118008 | ||||||
| chr2:152118072 | T | C | 1 | a0001c0001t0048 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2502A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2502 | chr2 | 152118072 | ||||||
| chr2:152118242 | C | A | 1 | a0001c0001t0047 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2332G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2332 | chr2 | 152118242 | ||||||
| chr2:152118408 | T | C | 2 | a0001c0001t0051 a0001c0001t0052 |
2 | HG02647.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2166A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2166 | chr2 | 152118408 | ||||||
| chr2:152118422 | G | A | 1 | a0001c0001t0041 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2152C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2152 | chr2 | 152118422 | ||||||
| chr2:152118432 | T | A | 1 | a0001c0001t0030 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2142A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2142 | chr2 | 152118432 | ||||||
| chr2:152118438 | C | CTA | 9 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0023 others(6): Show |
23 | HG00408.hp2 HG01256.hp2 HG01517.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2134_*2135dupTA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2135 | chr2 | 152118438 | ||||||
| chr2:152118438 | C | CTATA | 7 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0019 others(4): Show |
41 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2132_*2135dupTATA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2135 | chr2 | 152118438 | ||||||
| chr2:152118438 | C | CTATATA | 4 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0048 others(1): Show |
38 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2130_*2135dupTATA others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2135 | chr2 | 152118438 | ||||||
| chr2:152118438 | C | CTATATAT others(1): Show |
1 | a0001c0001t0024 | 3 | NA18950.hp2 NA18952.hp1 NA18973.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2135_*2136insTATA others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2135 | chr2 | 152118438 | ||||||
| chr2:152118443 | T | C | 1 | a0001c0001t0033 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2131A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2131 | chr2 | 152118443 | ||||||
| chr2:152118446 | T | A | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(43): Show |
231 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*2128A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2128 | chr2 | 152118446 | ||||||
| chr2:152118460 | A | ATATATAT others(1): Show |
1 | a0001c0001t0021 | 4 | HG00639.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2113_*2114insCATA others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2113 | chr2 | 152118460 | ||||||
| chr2:152118460 | A | ATATATG | 1 | a0001c0001t0020 | 4 | HG01891.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2113_*2114insCATA others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2113 | chr2 | 152118460 | ||||||
| chr2:152118460 | A | ATATG | 6 | a0001c0001t0027 a0001c0001t0042 a0001c0001t0043 others(3): Show |
9 | HG01070.hp2 HG01496.hp2 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2113_*2114insCATA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2113 | chr2 | 152118460 | ||||||
| chr2:152118460 | A | ATG | 3 | a0001c0001t0012 a0001c0001t0051 a0001c0001t0054 |
9 | HG00639.hp1 HG02572.hp1 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2112_*2113dupCA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2113 | chr2 | 152118460 | ||||||
| chr2:152118460 | A | G | 1 | a0001c0001t0031 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2114T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2114 | chr2 | 152118460 | ||||||
| chr2:152118639 | A | G | 1 | a0001c0001t0042 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1935T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1935 | chr2 | 152118639 | ||||||
| chr2:152118699 | AT | A | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 others(14): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1874delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1874 | chr2 | 152118699 | ||||||
| chr2:152118725 | T | A | 1 | a0001c0001t0011 | 7 | HG01192.hp2 HG02280.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1849A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1849 | chr2 | 152118725 | ||||||
| chr2:152118926 | A | G | 1 | a0001c0001t0034 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1648T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1648 | chr2 | 152118926 | ||||||
| chr2:152119037 | G | A | 3 | a0001c0001t0017 a0001c0001t0023 a0001c0001t0036 |
10 | HG00408.hp2 HG01256.hp2 HG01981.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1537C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1537 | chr2 | 152119037 | ||||||
| chr2:152119121 | T | G | 1 | a0001c0001t0044 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1453A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1453 | chr2 | 152119121 | ||||||
| chr2:152119296 | T | C | 1 | a0001c0001t0052 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1278A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1278 | chr2 | 152119296 | ||||||
| chr2:152119332 | A | G | 1 | a0001c0001t0039 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1242T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1242 | chr2 | 152119332 | ||||||
| chr2:152119488 | G | C | 19 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(16): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1086C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1086 | chr2 | 152119488 | ||||||
| chr2:152119597 | C | A | 1 | a0001c0001t0026 | 2 | HG03239.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*977G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 977 | chr2 | 152119597 | ||||||
| chr2:152119721 | A | T | 1 | a0001c0001t0030 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*853T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 853 | chr2 | 152119721 | ||||||
| chr2:152119722 | T | A | 1 | a0001c0001t0030 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*852A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 852 | chr2 | 152119722 | ||||||
| chr2:152119723 | A | G | 1 | a0001c0001t0030 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*851T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 851 | chr2 | 152119723 | ||||||
| chr2:152120079 | A | T | 1 | a0001c0001t0053 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*495T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 495 | chr2 | 152120079 | ||||||
| chr2:152120161 | T | G | 3 | a0001c0001t0017 a0001c0001t0023 a0001c0001t0036 |
10 | HG00408.hp2 HG01256.hp2 HG01981.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*413A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 413 | chr2 | 152120161 | ||||||
| chr2:152120189 | T | A | 50 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(47): Show |
249 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*385A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 385 | chr2 | 152120189 | ||||||
| chr2:152120222 | A | G | 4 | a0001c0001t0008 a0001c0001t0038 a0001c0001t0059 others(1): Show |
16 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*352T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 352 | chr2 | 152120222 | ||||||
| chr2:152120254 | T | A | 2 | a0001c0001t0051 a0001c0001t0052 |
2 | HG02647.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*320A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 320 | chr2 | 152120254 | ||||||
| chr2:152120317 | C | G | 1 | a0001c0001t0032 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*257G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 257 | chr2 | 152120317 | ||||||
| chr2:152120392 | A | T | 1 | a0001c0001t0037 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*182T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 182 | chr2 | 152120392 | ||||||
| chr2:152120395 | G | GA | 8 | a0001c0001t0015 a0001c0001t0022 a0001c0001t0023 others(5): Show |
19 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*178dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 178 | chr2 | 152120395 | ||||||
| chr2:152120395 | GA | G | 15 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(12): Show |
88 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*178delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 178 | chr2 | 152120395 | ||||||
| chr2:152120395 | GAA | G | 4 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0030 others(1): Show |
30 | HG00408.hp1 HG00673.hp1 HG01978.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*177_*178delTT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 177 | chr2 | 152120395 | ||||||
| chr2:152120407 | A | C | 1 | a0001c0001t0029 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*167T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 167 | chr2 | 152120407 | ||||||
| chr2:152120464 | C | A | 1 | a0001c0001t0057 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*110G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 110 | chr2 | 152120464 | ||||||
| chr2:152120544 | A | G | 2 | a0001c0001t0016 a0001c0001t0028 |
6 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*30T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 30 | chr2 | 152120544 | ||||||
| chr2:152120562 | C | T | 1 | a0001c0001t0028 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 12 | chr2 | 152120562 | ||||||
| chr2:152175694 | T | C | 4 | a0001c0001t0008 a0001c0001t0058 a0001c0001t0059 others(1): Show |
16 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-52A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/14 | 52 | chr2 | 152175694 | ||||||
| chr2:152175763 | T | G | 1 | a0001c0001t0061 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/14 | 121 | chr2 | 152175763 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:152120907 | T | TA | 7 | a0001c0001t0020g0155 a0001c0001t0020g0156 a0001c0001t0043g0157 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1350-106dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152120907 | |||||||
| chr2:152120948 | C | A | 2 | a0001c0001t0051g0095 a0001c0001t0052g0096 |
2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1350-146G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152120948 | |||||||
| chr2:152120963 | A | C | 1 | a0001c0001t0009g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1350-161T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152120963 | |||||||
| chr2:152121238 | C | T | 1 | a0001c0001t0007g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1350-436G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121238 | |||||||
| chr2:152121256 | G | A | 1 | a0001c0001t0017g0202 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1350-454C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121256 | |||||||
| chr2:152121447 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1350-645T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121447 | |||||||
| chr2:152121474 | G | A | 82 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(79): Show |
88 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1350-672C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121474 | |||||||
| chr2:152121646 | CTA | C | 5 | a0001c0001t0016g0028 a0001c0001t0016g0029 a0001c0001t0016g0104 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1350-846_1350-845d others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121646 | |||||||
| chr2:152121752 | T | C | 5 | a0001c0001t0002g0003 a0001c0001t0002g0078 a0001c0001t0002g0094 others(2): Show |
7 | NA18747.hp2 NA18941.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1350-950A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121752 | |||||||
| chr2:152121770 | A | C | 186 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(183): Show |
209 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.1350-968T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121770 | |||||||
| chr2:152121820 | G | A | 5 | a0001c0001t0016g0028 a0001c0001t0016g0029 a0001c0001t0016g0104 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1350-1018C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121820 | |||||||
| chr2:152121827 | G | A | 111 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0003g0018 others(108): Show |
118 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1350-1025C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121827 | |||||||
| chr2:152121919 | G | A | 12 | a0001c0001t0007g0010 a0001c0001t0007g0040 a0001c0001t0007g0115 others(9): Show |
14 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1350-1117C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121919 | |||||||
| chr2:152121921 | G | A | 2 | a0001c0001t0006g0127 a0001c0001t0061g0128 |
2 | NA18970.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1350-1119C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121921 | |||||||
| chr2:152121974 | G | C | 1 | a0001c0001t0011g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1350-1172C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121974 | |||||||
| chr2:152122049 | A | C | 18 | a0001c0001t0002g0074 a0001c0001t0008g0027 a0001c0001t0008g0305 others(15): Show |
19 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1350-1247T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122049 | |||||||
| chr2:152122057 | A | T | 23 | a0001c0001t0006g0149 a0001c0001t0007g0114 a0001c0001t0012g0159 others(20): Show |
23 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1350-1255T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122057 | |||||||
| chr2:152122057 | AAT | A | 24 | a0001c0001t0001g0257 a0001c0001t0002g0001 a0001c0001t0002g0087 others(21): Show |
25 | HG02145.hp1 HG02155.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.1350-1257_1350-125 others(6): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122057 | |||||||
| chr2:152122057 | AATAT | A | 73 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(70): Show |
87 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1350-1259_1350-125 others(8): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122057 | |||||||
| chr2:152122058 | AT | A | 6 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0034 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350-1257delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122058 | |||||||
| chr2:152122058 | ATAT | A | 3 | a0001c0001t0003g0246 a0001c0001t0014g0033 a0001c0001t0014g0036 |
3 | HG01167.hp2 HG02896.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1350-1259_1350-125 others(7): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122058 | |||||||
| chr2:152122059 | T | A | 79 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(76): Show |
85 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1350-1257A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122059 | |||||||
| chr2:152122061 | T | A | 86 | a0001c0001t0003g0018 a0001c0001t0003g0181 a0001c0001t0003g0182 others(83): Show |
92 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1350-1259A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122061 | |||||||
| chr2:152122063 | T | A | 2 | a0001c0001t0002g0074 a0001c0001t0003g0246 |
2 | HG03492.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1350-1261A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122063 | |||||||
| chr2:152122065 | T | A | 1 | a0001c0001t0003g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1350-1263A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122065 | |||||||
| chr2:152122072 | A | ATG | 9 | a0001c0001t0006g0300 a0001c0001t0007g0010 a0001c0001t0007g0115 others(6): Show |
11 | HG01891.hp1 HG02280.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1350-1271_1350-127 others(6): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122072 | |||||||
| chr2:152122072 | A | ATGTG | 4 | a0001c0001t0006g0139 a0001c0001t0007g0297 a0001c0001t0011g0142 others(1): Show |
4 | HG02647.hp1 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350-1271_1350-127 others(8): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122072 | |||||||
| chr2:152122072 | A | G | 4 | a0001c0001t0012g0159 a0001c0001t0027g0158 a0001c0001t0027g0162 others(1): Show |
4 | HG01070.hp2 HG01496.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350-1270T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122072 | |||||||
| chr2:152122074 | A | ATGTG | 16 | a0001c0001t0001g0137 a0001c0001t0006g0026 a0001c0001t0006g0127 others(13): Show |
17 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1350-1273_1350-127 others(8): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122074 | |||||||
| chr2:152122074 | A | G | 36 | a0001c0001t0006g0139 a0001c0001t0006g0300 a0001c0001t0007g0010 others(33): Show |
38 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1350-1272T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122074 | |||||||
| chr2:152122074 | ATATGTG | A | 78 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(75): Show |
84 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1350-1278_1350-127 others(10): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122074 | |||||||
| chr2:152122076 | A | ATG | 3 | a0001c0001t0007g0119 a0001c0001t0013g0290 a0001c0001t0039g0281 |
3 | HG02080.hp1 HG02683.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1350-1276_1350-127 others(6): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122076 | |||||||
| chr2:152122076 | A | G | 85 | a0001c0001t0001g0006 a0001c0001t0001g0132 a0001c0001t0001g0137 others(82): Show |
91 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.1350-1274T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122076 | |||||||
| chr2:152122076 | ATGTG | A | 7 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(4): Show |
7 | HG01167.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1350-1278_1350-127 others(8): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122076 | |||||||
| chr2:152122078 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0260 a0001c0001t0003g0246 |
4 | HG03688.hp2 NA18960.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350-1276C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122078 | |||||||
| chr2:152122145 | G | T | 1 | a0001c0001t0003g0221 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1350-1343C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122145 | |||||||
| chr2:152122166 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1350-1364G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122166 | |||||||
| chr2:152122289 | G | A | 96 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(93): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1349+1477C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122289 | |||||||
| chr2:152122330 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1349+1436A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122330 | |||||||
| chr2:152122349 | C | T | 1 | a0001c0001t0021g0168 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1349+1417G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122349 | |||||||
| chr2:152122433 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1349+1333T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122433 | |||||||
| chr2:152122488 | G | A | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1349+1278C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122488 | |||||||
| chr2:152122525 | C | T | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1349+1241G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122525 | |||||||
| chr2:152122558 | T | C | 1 | a0001c0001t0020g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1349+1208A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122558 | |||||||
| chr2:152122605 | T | A | 2 | a0001c0001t0003g0182 a0001c0001t0003g0235 |
2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1349+1161A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122605 | |||||||
| chr2:152123062 | C | A | 1 | a0001c0001t0001g0296 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1349+704G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123062 | |||||||
| chr2:152123094 | C | T | 1 | a0001c0001t0046g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1349+672G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123094 | |||||||
| chr2:152123134 | T | C | 255 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(252): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1349+632A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123134 | |||||||
| chr2:152123181 | C | A | 1 | a0001c0001t0001g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1349+585G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123181 | |||||||
| chr2:152123199 | G | A | 96 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(93): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1349+567C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123199 | |||||||
| chr2:152123232 | C | T | 2 | a0001c0001t0051g0095 a0001c0001t0052g0096 |
2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1349+534G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123232 | |||||||
| chr2:152123243 | G | A | 1 | a0001c0001t0007g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1349+523C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123243 | |||||||
| chr2:152123305 | G | A | 1 | a0001c0001t0003g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1349+461C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123305 | |||||||
| chr2:152123335 | G | GT | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1349+430_1349+431i others(3): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123335 | |||||||
| chr2:152123355 | G | C | 96 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(93): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1349+411C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123355 | |||||||
| chr2:152123358 | G | A | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1349+408C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123358 | |||||||
| chr2:152123411 | A | C | 1 | a0001c0001t0008g0310 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1349+355T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123411 | |||||||
| chr2:152123419 | C | T | 112 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(109): Show |
118 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1349+347G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123419 | |||||||
| chr2:152123464 | G | C | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1349+302C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123464 | |||||||
| chr2:152123504 | C | A | 1 | a0001c0001t0004g0236 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1349+262G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123504 | |||||||
| chr2:152123646 | C | T | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1349+120G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123646 | |||||||
| chr2:152123732 | C | T | 2 | a0001c0001t0002g0073 a0001c0001t0002g0074 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1349+34G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123732 | |||||||
| chr2:152123751 | G | C | 2 | a0001c0001t0051g0095 a0001c0001t0052g0096 |
2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1349+15C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123751 | |||||||
| chr2:152124063 | T | C | 1 | a0001c0001t0013g0253 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1180-128A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124063 | |||||||
| chr2:152124339 | T | A | 210 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(207): Show |
233 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.1180-404A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124339 | |||||||
| chr2:152124761 | A | C | 2 | a0001c0001t0027g0158 a0001c0001t0027g0162 |
2 | HG01070.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1180-826T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124761 | |||||||
| chr2:152124766 | C | T | 143 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(140): Show |
163 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1180-831G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124766 | |||||||
| chr2:152124821 | G | T | 96 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(93): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1180-886C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124821 | |||||||
| chr2:152124828 | C | T | 1 | a0001c0001t0056g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1180-893G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124828 | |||||||
| chr2:152124869 | T | C | 255 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(252): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1180-934A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124869 | |||||||
| chr2:152124889 | C | A | 1 | a0001c0001t0001g0263 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1180-954G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124889 | |||||||
| chr2:152124954 | T | C | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1180-1019A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124954 | |||||||
| chr2:152125041 | A | G | 6 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(3): Show |
6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-1106T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125041 | |||||||
| chr2:152125109 | A | C | 1 | a0001c0001t0046g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1179+1117T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125109 | |||||||
| chr2:152125313 | G | A | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1179+913C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125313 | |||||||
| chr2:152125492 | T | C | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1179+734A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125492 | |||||||
| chr2:152125547 | G | GT | 3 | a0001c0001t0001g0113 a0001c0001t0015g0111 a0001c0001t0015g0112 |
3 | HG02055.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1179+678dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125547 | |||||||
| chr2:152125691 | T | C | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1179+535A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125691 | |||||||
| chr2:152125910 | G | T | 80 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(77): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1179+316C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125910 | |||||||
| chr2:152126057 | G | C | 1 | a0001c0001t0005g0067 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1179+169C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152126057 | |||||||
| chr2:152126516 | C | T | 1 | a0001c0001t0014g0031 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1026-137G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126516 | |||||||
| chr2:152126536 | G | T | 1 | a0001c0001t0005g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1026-157C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126536 | |||||||
| chr2:152126570 | T | C | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1026-191A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126570 | |||||||
| chr2:152126692 | A | T | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1026-313T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126692 | |||||||
| chr2:152126712 | A | AC | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1026-334dupG | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126712 | |||||||
| chr2:152126765 | A | T | 11 | a0001c0001t0009g0038 a0001c0001t0009g0041 a0001c0001t0009g0042 others(8): Show |
11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1026-386T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126765 | |||||||
| chr2:152126852 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1026-473C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126852 | |||||||
| chr2:152127196 | A | G | 7 | a0001c0001t0020g0155 a0001c0001t0020g0156 a0001c0001t0043g0157 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026-817T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127196 | |||||||
| chr2:152127234 | TG | T | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1026-856delC | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127234 | |||||||
| chr2:152127401 | A | C | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1026-1022T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127401 | |||||||
| chr2:152127687 | T | C | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1026-1308A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127687 | |||||||
| chr2:152127719 | C | T | 2 | a0001c0001t0019g0194 a0001c0001t0037g0197 |
2 | NA18963.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1026-1340G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127719 | |||||||
| chr2:152127797 | A | T | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1026-1418T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127797 | |||||||
| chr2:152127849 | T | C | 1 | a0001c0001t0044g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1026-1470A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127849 | |||||||
| chr2:152128000 | C | T | 9 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(6): Show |
9 | HG00639.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-1621G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128000 | |||||||
| chr2:152128051 | C | T | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1026-1672G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128051 | |||||||
| chr2:152128130 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1026-1751C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128130 | |||||||
| chr2:152128399 | C | T | 1 | a0001c0001t0006g0129 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1026-2020G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128399 | |||||||
| chr2:152128417 | T | TA | 4 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0267 others(1): Show |
7 | HG02056.hp1 NA18747.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026-2039dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128417 | |||||||
| chr2:152128418 | A | T | 2 | a0001c0001t0005g0090 a0001c0001t0005g0091 |
2 | NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1026-2039T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128418 | |||||||
| chr2:152128460 | GA | G | 15 | a0001c0001t0008g0027 a0001c0001t0008g0305 a0001c0001t0008g0306 others(12): Show |
16 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1026-2082delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128460 | |||||||
| chr2:152128599 | T | C | 1 | a0001c0001t0025g0085 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1026-2220A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128599 | |||||||
| chr2:152128643 | C | T | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1026-2264G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128643 | |||||||
| chr2:152128885 | T | TAGGAATA others(5): Show |
1 | a0001c0001t0001g0288 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1026-2518_1026-250 others(16): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128885 | |||||||
| chr2:152128965 | G | C | 1 | a0001c0001t0039g0281 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1026-2586C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128965 | |||||||
| chr2:152129055 | T | G | 1 | a0001c0001t0007g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1026-2676A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129055 | |||||||
| chr2:152129527 | T | C | 92 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(89): Show |
98 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1025+2587A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129527 | |||||||
| chr2:152129667 | C | T | 2 | a0001c0001t0003g0181 a0001c0001t0003g0242 |
2 | HG04184.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1025+2447G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129667 | |||||||
| chr2:152129686 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1025+2428G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129686 | |||||||
| chr2:152129740 | A | C | 1 | a0001c0001t0044g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1025+2374T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129740 | |||||||
| chr2:152129749 | A | C | 1 | a0001c0001t0041g0286 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1025+2365T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129749 | |||||||
| chr2:152129784 | C | T | 4 | a0001c0001t0009g0046 a0001c0001t0009g0047 a0001c0001t0009g0048 others(1): Show |
4 | HG02145.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+2330G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129784 | |||||||
| chr2:152129832 | T | C | 1 | a0001c0001t0044g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1025+2282A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129832 | |||||||
| chr2:152129838 | A | G | 1 | a0001c0001t0008g0309 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1025+2276T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129838 | |||||||
| chr2:152129862 | T | C | 5 | a0001c0001t0016g0028 a0001c0001t0016g0029 a0001c0001t0016g0104 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025+2252A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129862 | |||||||
| chr2:152129985 | A | G | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1025+2129T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129985 | |||||||
| chr2:152130079 | C | T | 80 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(77): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1025+2035G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130079 | |||||||
| chr2:152130095 | A | G | 2 | a0001c0001t0016g0028 a0001c0001t0016g0029 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1025+2019T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130095 | |||||||
| chr2:152130288 | T | G | 11 | a0001c0001t0009g0038 a0001c0001t0009g0041 a0001c0001t0009g0042 others(8): Show |
11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1025+1826A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130288 | |||||||
| chr2:152130290 | T | C | 11 | a0001c0001t0009g0038 a0001c0001t0009g0041 a0001c0001t0009g0042 others(8): Show |
11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1025+1824A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130290 | |||||||
| chr2:152130337 | C | T | 1 | a0001c0001t0004g0240 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1025+1777G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130337 | |||||||
| chr2:152130465 | A | G | 1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1025+1649T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130465 | |||||||
| chr2:152130541 | G | A | 4 | a0001c0001t0008g0306 a0001c0001t0008g0307 a0001c0001t0008g0310 others(1): Show |
4 | HG01081.hp1 HG01109.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+1573C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130541 | |||||||
| chr2:152130542 | C | T | 62 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(59): Show |
78 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1025+1572G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130542 | |||||||
| chr2:152130694 | A | T | 3 | a0001c0001t0020g0170 a0001c0001t0021g0171 a0001c0001t0021g0172 |
3 | HG02257.hp2 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1025+1420T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130694 | |||||||
| chr2:152130995 | CA | C | 298 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(295): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1025+1118delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130995 | |||||||
| chr2:152131032 | A | C | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1025+1082T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152131032 | |||||||
| chr2:152131589 | T | C | 12 | a0001c0001t0007g0010 a0001c0001t0007g0040 a0001c0001t0007g0115 others(9): Show |
14 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1025+525A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152131589 | |||||||
| chr2:152131619 | G | C | 2 | a0001c0001t0051g0095 a0001c0001t0052g0096 |
2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1025+495C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152131619 | |||||||
| chr2:152131635 | G | A | 1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1025+479C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152131635 | |||||||
| chr2:152131755 | G | C | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1025+359C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152131755 | |||||||
| chr2:152131872 | T | C | 1 | a0001c0001t0038g0092 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1025+242A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152131872 | |||||||
| chr2:152132044 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1025+70A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152132044 | |||||||
| chr2:152132096 | C | CT | 210 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(207): Show |
233 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.1025+17dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152132096 | |||||||
| chr2:152132101 | C | T | 1 | a0001c0001t0020g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1025+13G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152132101 | |||||||
| chr2:152132242 | A | G | 3 | a0001c0001t0004g0251 a0001c0001t0019g0194 a0001c0001t0037g0197 |
3 | NA18963.hp1 NA19005.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.971-74T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 10/13 | chr2 | 152132242 | |||||||
| chr2:152132515 | T | C | 3 | a0001c0001t0007g0118 a0001c0001t0007g0119 a0001c0001t0007g0123 |
3 | HG02717.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.971-347A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 10/13 | chr2 | 152132515 | |||||||
| chr2:152132628 | T | C | 1 | a0001c0001t0002g0079 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.971-460A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 10/13 | chr2 | 152132628 | |||||||
| chr2:152132663 | TAAG | T | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.971-498_971-496del others(3): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 10/13 | chr2 | 152132663 | |||||||
| chr2:152132785 | CTA | C | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.970+386_970+387del others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 10/13 | chr2 | 152132785 | |||||||
| chr2:152133000 | G | A | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.970+173C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 10/13 | chr2 | 152133000 | |||||||
| chr2:152133537 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0015g0111 a0001c0001t0015g0112 |
3 | HG02055.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.800-53C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152133537 | |||||||
| chr2:152133790 | T | C | 1 | a0001c0001t0020g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.800-306A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152133790 | |||||||
| chr2:152133844 | G | A | 1 | a0001c0001t0003g0201 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.800-360C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152133844 | |||||||
| chr2:152133932 | C | G | 1 | a0001c0001t0046g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.800-448G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152133932 | |||||||
| chr2:152134007 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.800-523A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134007 | |||||||
| chr2:152134104 | TG | T | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.800-621delC | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134104 | |||||||
| chr2:152134207 | T | C | 3 | a0001c0001t0007g0120 a0001c0001t0007g0121 a0001c0001t0007g0122 |
3 | HG02109.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.800-723A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134207 | |||||||
| chr2:152134207 | T | G | 80 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(77): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.800-723A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134207 | |||||||
| chr2:152134352 | C | T | 1 | a0001c0001t0003g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.800-868G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134352 | |||||||
| chr2:152134418 | A | G | 210 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(207): Show |
233 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.800-934T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134418 | |||||||
| chr2:152134449 | C | T | 1 | a0001c0001t0003g0249 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.800-965G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134449 | |||||||
| chr2:152134841 | G | A | 2 | a0001c0001t0003g0226 a0001c0002t0018g0153 |
2 | HG03540.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.799+668C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134841 | |||||||
| chr2:152134930 | G | A | 1 | a0001c0001t0007g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.799+579C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134930 | |||||||
| chr2:152134946 | T | C | 1 | a0001c0001t0046g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.799+563A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134946 | |||||||
| chr2:152134988 | G | T | 1 | a0001c0001t0033g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.799+521C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134988 | |||||||
| chr2:152134993 | C | T | 5 | a0001c0001t0013g0025 a0001c0001t0013g0253 a0001c0001t0013g0290 others(2): Show |
6 | HG01074.hp1 HG01192.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.799+516G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134993 | |||||||
| chr2:152135401 | AT | A | 98 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(95): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.799+107delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152135401 | |||||||
| chr2:152135449 | A | G | 1 | a0001c0001t0007g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.799+60T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152135449 | |||||||
| chr2:152135651 | C | CAATA | 64 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(61): Show |
80 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.705-52_705-49dupTA others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135651 | |||||||
| chr2:152135723 | G | A | 186 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(183): Show |
209 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.705-120C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135723 | |||||||
| chr2:152135781 | C | T | 1 | a0001c0001t0016g0106 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.705-178G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135781 | |||||||
| chr2:152135856 | A | G | 1 | a0001c0001t0026g0022 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.705-253T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135856 | |||||||
| chr2:152135868 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.705-265A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135868 | |||||||
| chr2:152135919 | A | G | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.705-316T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135919 | |||||||
| chr2:152135998 | G | A | 186 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(183): Show |
209 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.705-395C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135998 | |||||||
| chr2:152136005 | G | A | 2 | a0001c0001t0004g0195 a0001c0001t0004g0203 |
2 | NA18974.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.705-402C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136005 | |||||||
| chr2:152136088 | C | CA | 10 | a0001c0001t0001g0137 a0001c0001t0001g0274 a0001c0001t0003g0218 others(7): Show |
10 | HG00621.hp2 HG00741.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.705-486dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136088 | |||||||
| chr2:152136088 | CA | C | 6 | a0001c0001t0001g0265 a0001c0001t0001g0282 a0001c0001t0003g0226 others(3): Show |
6 | HG01069.hp1 HG01943.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.705-486delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136088 | |||||||
| chr2:152136214 | G | A | 2 | a0001c0001t0027g0158 a0001c0001t0027g0162 |
2 | HG01070.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.705-611C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136214 | |||||||
| chr2:152136246 | T | A | 1 | a0001c0001t0001g0021 | 2 | NA18944.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.705-643A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136246 | |||||||
| chr2:152136262 | G | A | 1 | a0001c0001t0060g0312 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.705-659C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136262 | |||||||
| chr2:152136515 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.705-912G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136515 | |||||||
| chr2:152136784 | C | T | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.705-1181G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136784 | |||||||
| chr2:152136892 | C | CT | 8 | a0001c0001t0001g0274 a0001c0001t0001g0284 a0001c0001t0002g0060 others(5): Show |
8 | HG00741.hp1 HG01261.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.705-1290dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136892 | |||||||
| chr2:152136892 | CT | C | 24 | a0001c0001t0005g0039 a0001c0001t0012g0159 a0001c0001t0012g0160 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.705-1290delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136892 | |||||||
| chr2:152136897 | T | C | 90 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(87): Show |
96 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.705-1294A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136897 | |||||||
| chr2:152136900 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.705-1297A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136900 | |||||||
| chr2:152137337 | G | C | 6 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(3): Show |
6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.705-1734C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152137337 | |||||||
| chr2:152137596 | T | C | 122 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(119): Show |
139 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.705-1993A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152137596 | |||||||
| chr2:152137602 | T | C | 11 | a0001c0001t0009g0038 a0001c0001t0009g0041 a0001c0001t0009g0042 others(8): Show |
11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.705-1999A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152137602 | |||||||
| chr2:152137738 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.705-2135A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152137738 | |||||||
| chr2:152137818 | T | G | 1 | a0001c0001t0002g0075 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.705-2215A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152137818 | |||||||
| chr2:152138100 | G | T | 6 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(3): Show |
6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.705-2497C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138100 | |||||||
| chr2:152138216 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.705-2613A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138216 | |||||||
| chr2:152138330 | T | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0288 a0001c0001t0015g0287 |
5 | HG02055.hp1 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.705-2727A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138330 | |||||||
| chr2:152138401 | T | G | 1 | a0001c0001t0001g0261 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.705-2798A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138401 | |||||||
| chr2:152138456 | T | C | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | NA18981.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.705-2853A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138456 | |||||||
| chr2:152138663 | C | T | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.705-3060G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138663 | |||||||
| chr2:152138747 | T | G | 80 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(77): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.705-3144A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138747 | |||||||
| chr2:152138755 | T | C | 3 | a0001c0001t0007g0120 a0001c0001t0007g0121 a0001c0001t0007g0122 |
3 | HG02109.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.705-3152A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138755 | |||||||
| chr2:152138948 | C | A | 1 | a0001c0001t0030g0057 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.705-3345G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138948 | |||||||
| chr2:152139031 | C | T | 1 | a0001c0001t0006g0134 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.705-3428G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139031 | |||||||
| chr2:152139197 | T | G | 6 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(3): Show |
6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.705-3594A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139197 | |||||||
| chr2:152139380 | G | C | 1 | a0001c0001t0001g0258 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.705-3777C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139380 | |||||||
| chr2:152139445 | T | C | 1 | a0001c0001t0007g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.705-3842A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139445 | |||||||
| chr2:152139841 | A | G | 2 | a0001c0001t0017g0196 a0001c0001t0017g0202 |
2 | NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.704+3986T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139841 | |||||||
| chr2:152139858 | TAATACAA others(15): Show |
T | 3 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 |
3 | HG02630.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.704+3947_704+3968d others(24): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139858 | |||||||
| chr2:152139902 | T | C | 3 | a0001c0001t0002g0086 a0001c0001t0002g0100 a0001c0001t0058g0304 |
3 | HG02027.hp2 HG02165.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.704+3925A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139902 | |||||||
| chr2:152139911 | C | G | 1 | a0001c0001t0046g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.704+3916G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139911 | |||||||
| chr2:152139991 | C | T | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.704+3836G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139991 | |||||||
| chr2:152140005 | G | A | 1 | a0001c0001t0022g0230 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.704+3822C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152140005 | |||||||
| chr2:152140460 | C | T | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.704+3367G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152140460 | |||||||
| chr2:152140905 | C | T | 80 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(77): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.704+2922G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152140905 | |||||||
| chr2:152140990 | T | A | 1 | a0001c0001t0008g0316 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.704+2837A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152140990 | |||||||
| chr2:152141040 | G | A | 1 | a0001c0001t0008g0316 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.704+2787C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141040 | |||||||
| chr2:152141138 | C | CAA | 6 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(3): Show |
6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.704+2687_704+2688d others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141138 | |||||||
| chr2:152141138 | CA | C | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.704+2688delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141138 | |||||||
| chr2:152141138 | CAA | C | 13 | a0001c0001t0001g0137 a0001c0001t0001g0277 a0001c0001t0002g0060 others(10): Show |
13 | HG01106.hp1 HG01123.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.704+2687_704+2688d others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141138 | |||||||
| chr2:152141212 | G | A | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.704+2615C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141212 | |||||||
| chr2:152141288 | C | A | 1 | a0001c0001t0007g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.704+2539G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141288 | |||||||
| chr2:152141459 | A | G | 1 | a0001c0001t0007g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.704+2368T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141459 | |||||||
| chr2:152141521 | A | G | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.704+2306T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141521 | |||||||
| chr2:152141545 | T | C | 1 | a0001c0001t0017g0196 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.704+2282A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141545 | |||||||
| chr2:152141558 | C | A | 1 | a0001c0001t0044g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.704+2269G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141558 | |||||||
| chr2:152141574 | A | C | 1 | a0001c0001t0016g0106 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.704+2253T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141574 | |||||||
| chr2:152141581 | T | G | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.704+2246A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141581 | |||||||
| chr2:152141592 | T | C | 14 | a0001c0001t0008g0027 a0001c0001t0008g0305 a0001c0001t0008g0306 others(11): Show |
15 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.704+2235A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141592 | |||||||
| chr2:152141629 | C | T | 2 | a0001c0001t0007g0010 a0001c0001t0007g0297 |
4 | HG02922.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+2198G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141629 | |||||||
| chr2:152141639 | G | C | 2 | a0001c0001t0007g0010 a0001c0001t0007g0297 |
4 | HG02922.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+2188C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141639 | |||||||
| chr2:152141674 | T | G | 1 | a0001c0001t0003g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.704+2153A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141674 | |||||||
| chr2:152141717 | A | G | 5 | a0001c0001t0016g0028 a0001c0001t0016g0029 a0001c0001t0016g0104 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.704+2110T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141717 | |||||||
| chr2:152141739 | C | T | 1 | a0001c0001t0009g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.704+2088G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141739 | |||||||
| chr2:152141751 | C | T | 1 | a0001c0001t0038g0092 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.704+2076G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141751 | |||||||
| chr2:152141811 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.704+2016C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141811 | |||||||
| chr2:152141929 | TTTCAAGG others(3): Show |
T | 2 | a0001c0001t0002g0003 a0001c0001t0025g0085 |
4 | NA18941.hp2 NA18983.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.704+1888_704+1897d others(12): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141929 | |||||||
| chr2:152141953 | T | C | 98 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(95): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.704+1874A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141953 | |||||||
| chr2:152141972 | C | T | 1 | a0001c0001t0015g0112 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.704+1855G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141972 | |||||||
| chr2:152142038 | G | A | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.704+1789C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142038 | |||||||
| chr2:152142082 | C | T | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.704+1745G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142082 | |||||||
| chr2:152142087 | G | A | 7 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(4): Show |
7 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+1740C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142087 | |||||||
| chr2:152142209 | T | G | 1 | a0001c0001t0007g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.704+1618A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142209 | |||||||
| chr2:152142316 | A | G | 1 | a0001c0001t0056g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.704+1511T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142316 | |||||||
| chr2:152142480 | G | C | 1 | a0001c0001t0007g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.704+1347C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142480 | |||||||
| chr2:152142547 | T | A | 3 | a0001c0001t0020g0170 a0001c0001t0021g0171 a0001c0001t0021g0172 |
3 | HG02257.hp2 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.704+1280A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142547 | |||||||
| chr2:152142622 | A | T | 1 | a0001c0001t0002g0053 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.704+1205T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142622 | |||||||
| chr2:152142623 | T | A | 1 | a0001c0001t0002g0053 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.704+1204A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142623 | |||||||
| chr2:152142625 | A | G | 1 | a0001c0001t0002g0053 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.704+1202T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142625 | |||||||
| chr2:152142833 | T | C | 1 | a0001c0001t0021g0172 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.704+994A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142833 | |||||||
| chr2:152142853 | T | C | 1 | a0001c0001t0016g0105 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.704+974A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142853 | |||||||
| chr2:152143111 | A | G | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.704+716T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152143111 | |||||||
| chr2:152143179 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.704+648G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152143179 | |||||||
| chr2:152143339 | A | G | 2 | a0001c0001t0003g0188 a0001c0001t0003g0247 |
2 | HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.704+488T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152143339 | |||||||
| chr2:152143576 | T | C | 4 | a0001c0001t0001g0258 a0001c0001t0001g0293 a0001c0001t0015g0275 others(1): Show |
5 | HG01168.hp2 HG02735.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.704+251A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152143576 | |||||||
| chr2:152143619 | A | T | 2 | a0001c0001t0007g0115 a0001c0001t0055g0116 |
2 | HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.704+208T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152143619 | |||||||
| chr2:152143823 | T | A | 255 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(252): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
splice_region_variant&intron_variant | LOW | c.704+4A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152143823 | |||||||
| chr2:152144081 | T | C | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.518-68A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144081 | |||||||
| chr2:152144199 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.518-186A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144199 | |||||||
| chr2:152144421 | T | C | 1 | a0001c0001t0003g0229 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.518-408A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144421 | |||||||
| chr2:152144462 | T | C | 11 | a0001c0001t0009g0038 a0001c0001t0009g0041 a0001c0001t0009g0042 others(8): Show |
11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+426A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144462 | |||||||
| chr2:152144532 | C | T | 1 | a0001c0001t0003g0247 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.517+356G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144532 | |||||||
| chr2:152144564 | G | C | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.517+324C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144564 | |||||||
| chr2:152144595 | G | C | 1 | a0001c0001t0003g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.517+293C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144595 | |||||||
| chr2:152144607 | T | C | 210 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(207): Show |
233 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.517+281A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144607 | |||||||
| chr2:152144683 | C | T | 2 | a0001c0001t0002g0078 a0001c0001t0002g0101 |
2 | NA18747.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.517+205G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144683 | |||||||
| chr2:152144684 | G | A | 3 | a0001c0001t0007g0118 a0001c0001t0007g0119 a0001c0001t0007g0123 |
3 | HG02717.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.517+204C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144684 | |||||||
| chr2:152144828 | C | T | 1 | a0001c0001t0046g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.517+60G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144828 | |||||||
| chr2:152144845 | GAT | G | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.517+41_517+42delAT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144845 | |||||||
| chr2:152145096 | G | C | 1 | a0001c0001t0008g0313 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.448-139C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145096 | |||||||
| chr2:152145128 | T | C | 1 | a0001c0001t0021g0172 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.448-171A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145128 | |||||||
| chr2:152145232 | G | A | 1 | a0001c0001t0003g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.448-275C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145232 | |||||||
| chr2:152145280 | G | T | 167 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(164): Show |
187 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.448-323C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145280 | |||||||
| chr2:152145405 | G | GT | 14 | a0001c0001t0008g0027 a0001c0001t0008g0305 a0001c0001t0008g0306 others(11): Show |
15 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.448-449dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145405 | |||||||
| chr2:152145544 | A | T | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.448-587T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145544 | |||||||
| chr2:152145986 | T | C | 1 | a0001c0001t0041g0286 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.448-1029A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145986 | |||||||
| chr2:152146113 | T | C | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.447+1049A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146113 | |||||||
| chr2:152146271 | C | CA | 70 | a0001c0001t0001g0113 a0001c0001t0001g0132 a0001c0001t0002g0054 others(67): Show |
73 | HG00140.hp2 HG00280.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.447+890dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146271 | |||||||
| chr2:152146271 | C | CAA | 81 | a0001c0001t0001g0137 a0001c0001t0003g0018 a0001c0001t0003g0178 others(78): Show |
87 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.447+889_447+890dup others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146271 | |||||||
| chr2:152146271 | C | CAAAA | 7 | a0001c0001t0003g0246 a0001c0001t0014g0031 a0001c0001t0014g0032 others(4): Show |
7 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.447+887_447+890dup others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146271 | |||||||
| chr2:152146271 | CA | C | 17 | a0001c0001t0001g0019 a0001c0001t0001g0254 a0001c0001t0001g0256 others(14): Show |
19 | HG01069.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.447+890delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146271 | |||||||
| chr2:152146291 | T | A | 1 | a0001c0001t0002g0053 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.447+871A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146291 | |||||||
| chr2:152146292 | C | T | 1 | a0001c0001t0002g0053 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.447+870G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146292 | |||||||
| chr2:152146293 | T | C | 1 | a0001c0001t0002g0053 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.447+869A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146293 | |||||||
| chr2:152146348 | G | A | 1 | a0001c0001t0011g0141 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.447+814C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146348 | |||||||
| chr2:152146413 | A | G | 1 | a0001c0001t0003g0226 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.447+749T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146413 | |||||||
| chr2:152146590 | G | C | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.447+572C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146590 | |||||||
| chr2:152146760 | G | A | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.447+402C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146760 | |||||||
| chr2:152146877 | G | T | 1 | a0001c0001t0003g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.447+285C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146877 | |||||||
| chr2:152146885 | G | A | 1 | a0001c0001t0010g0083 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.447+277C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146885 | |||||||
| chr2:152146898 | T | C | 80 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(77): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.447+264A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146898 | |||||||
| chr2:152146932 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.447+230C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146932 | |||||||
| chr2:152146957 | T | C | 1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.447+205A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146957 | |||||||
| chr2:152147069 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.447+93A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152147069 | |||||||
| chr2:152147421 | A | C | 1 | a0001c0001t0004g0207 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.301-113T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147421 | |||||||
| chr2:152147634 | T | C | 5 | a0001c0001t0003g0181 a0001c0001t0003g0242 a0001c0001t0004g0240 others(2): Show |
5 | HG00609.hp1 HG04184.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-326A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147634 | |||||||
| chr2:152147700 | T | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(4): Show |
12 | HG00140.hp1 HG01123.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+324A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147700 | |||||||
| chr2:152147739 | G | A | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.300+285C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147739 | |||||||
| chr2:152147758 | A | G | 2 | a0001c0001t0044g0180 a0001c0001t0046g0176 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.300+266T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147758 | |||||||
| chr2:152147768 | A | G | 3 | a0001c0001t0007g0120 a0001c0001t0007g0121 a0001c0001t0007g0122 |
3 | HG02109.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.300+256T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147768 | |||||||
| chr2:152147804 | C | G | 1 | a0001c0001t0005g0107 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.300+220G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147804 | |||||||
| chr2:152147832 | A | G | 6 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(3): Show |
6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.300+192T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147832 | |||||||
| chr2:152147871 | C | A | 255 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(252): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.300+153G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147871 | |||||||
| chr2:152147982 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.300+42T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147982 | |||||||
| chr2:152148167 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0288 a0001c0001t0015g0287 |
5 | HG02055.hp1 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-45T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 3/13 | chr2 | 152148167 | |||||||
| chr2:152148222 | C | T | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
splice_region_variant&intron_variant | LOW | c.201+3G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 3/13 | chr2 | 152148222 | |||||||
| chr2:152148453 | T | C | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.126-153A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152148453 | |||||||
| chr2:152148970 | G | A | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.126-670C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152148970 | |||||||
| chr2:152149330 | A | G | 184 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(181): Show |
207 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.125+815T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149330 | |||||||
| chr2:152149432 | C | G | 98 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(95): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.125+713G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149432 | |||||||
| chr2:152149490 | T | C | 1 | a0001c0001t0007g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.125+655A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149490 | |||||||
| chr2:152149496 | CT | C | 175 | a0001c0001t0001g0255 a0001c0001t0001g0265 a0001c0001t0002g0001 others(172): Show |
198 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.125+648delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149496 | |||||||
| chr2:152149496 | CTT | C | 10 | a0001c0001t0004g0186 a0001c0001t0014g0031 a0001c0001t0014g0032 others(7): Show |
10 | HG01167.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.125+647_125+648del others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149496 | |||||||
| chr2:152149525 | T | C | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.125+620A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149525 | |||||||
| chr2:152149549 | G | A | 1 | a0001c0001t0008g0317 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.125+596C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149549 | |||||||
| chr2:152149573 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG01123.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.125+572G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149573 | |||||||
| chr2:152149745 | G | A | 1 | a0001c0001t0005g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.125+400C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149745 | |||||||
| chr2:152149867 | T | C | 9 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(6): Show |
9 | HG00639.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.125+278A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149867 | |||||||
| chr2:152149938 | G | C | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.125+207C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149938 | |||||||
| chr2:152150019 | T | G | 1 | a0001c0001t0044g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.125+126A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152150019 | |||||||
| chr2:152150049 | T | C | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.125+96A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152150049 | |||||||
| chr2:152150090 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.125+55C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152150090 | |||||||
| chr2:152150286 | T | C | 1 | a0001c0001t0050g0081 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.41-57A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152150286 | |||||||
| chr2:152150519 | C | T | 1 | a0001c0001t0044g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.41-290G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152150519 | |||||||
| chr2:152150520 | A | G | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-291T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152150520 | |||||||
| chr2:152151048 | G | A | 2 | a0001c0001t0010g0082 a0001c0001t0010g0083 |
2 | NA18982.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.41-819C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151048 | |||||||
| chr2:152151093 | G | C | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-864C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151093 | |||||||
| chr2:152151178 | C | CT | 12 | a0001c0001t0001g0268 a0001c0001t0007g0118 a0001c0001t0007g0119 others(9): Show |
12 | HG01167.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.41-950dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151178 | |||||||
| chr2:152151178 | CT | C | 8 | a0001c0001t0001g0254 a0001c0001t0007g0010 a0001c0001t0007g0115 others(5): Show |
10 | HG01891.hp1 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.41-950delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151178 | |||||||
| chr2:152151196 | T | C | 96 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(93): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.41-967A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151196 | |||||||
| chr2:152151196 | T | TC | 4 | a0001c0001t0005g0070 a0001c0001t0016g0104 a0001c0001t0016g0105 others(1): Show |
4 | HG02486.hp2 HG03225.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-968dupG | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151196 | |||||||
| chr2:152151349 | T | C | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-1120A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151349 | |||||||
| chr2:152151422 | C | T | 3 | a0001c0001t0004g0251 a0001c0001t0010g0082 a0001c0001t0010g0083 |
3 | NA18982.hp1 NA18994.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.41-1193G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151422 | |||||||
| chr2:152151511 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0023 |
5 | HG00140.hp1 HG01123.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-1282C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151511 | |||||||
| chr2:152151573 | T | C | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-1344A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151573 | |||||||
| chr2:152151609 | T | C | 2 | a0001c0001t0016g0028 a0001c0001t0016g0029 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.41-1380A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151609 | |||||||
| chr2:152151692 | C | G | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-1463G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151692 | |||||||
| chr2:152151737 | G | A | 1 | a0001c0001t0004g0251 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.41-1508C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151737 | |||||||
| chr2:152152192 | C | T | 98 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(95): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-1963G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152192 | |||||||
| chr2:152152279 | G | A | 1 | a0001c0002t0018g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.41-2050C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152279 | |||||||
| chr2:152152363 | C | T | 1 | a0001c0001t0034g0064 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.41-2134G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152363 | |||||||
| chr2:152152403 | C | G | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-2174G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152403 | |||||||
| chr2:152152406 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.41-2177C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152406 | |||||||
| chr2:152152422 | G | A | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.41-2193C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152422 | |||||||
| chr2:152152427 | T | C | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-2198A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152427 | |||||||
| chr2:152152474 | G | A | 1 | a0001c0001t0035g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.41-2245C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152474 | |||||||
| chr2:152152555 | A | C | 1 | a0001c0001t0036g0209 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.41-2326T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152555 | |||||||
| chr2:152152561 | C | CA | 92 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(89): Show |
98 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.41-2333dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152561 | |||||||
| chr2:152152603 | C | T | 3 | a0001c0001t0012g0160 a0001c0001t0051g0095 a0001c0001t0052g0096 |
3 | HG02647.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.41-2374G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152603 | |||||||
| chr2:152152617 | A | G | 255 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(252): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.41-2388T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152617 | |||||||
| chr2:152152895 | C | T | 255 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(252): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.41-2666G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152895 | |||||||
| chr2:152152955 | A | G | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-2726T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152955 | |||||||
| chr2:152153133 | CT | C | 2 | a0001c0001t0007g0010 a0001c0001t0007g0297 |
4 | HG02922.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-2905delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153133 | |||||||
| chr2:152153150 | A | G | 6 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(3): Show |
6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-2921T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153150 | |||||||
| chr2:152153171 | T | C | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.41-2942A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153171 | |||||||
| chr2:152153271 | C | G | 1 | a0001c0001t0020g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.41-3042G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153271 | |||||||
| chr2:152153303 | T | C | 1 | a0001c0001t0059g0314 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.41-3074A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153303 | |||||||
| chr2:152153397 | A | G | 5 | a0001c0001t0016g0028 a0001c0001t0016g0029 a0001c0001t0016g0104 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-3168T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153397 | |||||||
| chr2:152153406 | A | T | 3 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 |
3 | HG02630.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.41-3177T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153406 | |||||||
| chr2:152153646 | A | G | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.41-3417T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153646 | |||||||
| chr2:152153793 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.41-3564A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153793 | |||||||
| chr2:152153885 | T | TAC | 38 | a0001c0001t0001g0008 a0001c0001t0001g0268 a0001c0001t0001g0269 others(35): Show |
42 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.41-3658_41-3657dup others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | |||||||
| chr2:152153885 | T | TACAC | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.41-3660_41-3657dup others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | |||||||
| chr2:152153885 | T | TACACAC | 24 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0137 others(21): Show |
26 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.41-3662_41-3657dup others(6): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | |||||||
| chr2:152153885 | T | TACACACA others(1): Show |
13 | a0001c0001t0001g0255 a0001c0001t0006g0138 a0001c0001t0006g0299 others(10): Show |
13 | HG01123.hp2 HG01358.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.41-3664_41-3657dup others(8): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | |||||||
| chr2:152153885 | T | TACACACA others(3): Show |
3 | a0001c0001t0006g0134 a0001c0001t0011g0146 a0001c0001t0015g0285 |
3 | HG00280.hp2 HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.41-3666_41-3657dup others(10): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | |||||||
| chr2:152153885 | TAC | T | 80 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0181 others(77): Show |
86 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.41-3658_41-3657del others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | |||||||
| chr2:152153885 | TACAC | T | 5 | a0001c0001t0005g0066 a0001c0001t0007g0010 a0001c0001t0007g0115 others(2): Show |
7 | HG02922.hp2 HG03098.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-3660_41-3657del others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | |||||||
| chr2:152153885 | TACACAC | T | 5 | a0001c0001t0016g0028 a0001c0001t0016g0029 a0001c0001t0016g0104 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-3662_41-3657del others(6): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | |||||||
| chr2:152153911 | C | CACAA | 6 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(3): Show |
6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-3683_41-3682ins others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153911 | |||||||
| chr2:152153919 | C | T | 1 | a0001c0001t0016g0105 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.41-3690G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153919 | |||||||
| chr2:152154214 | T | C | 1 | a0001c0001t0046g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.41-3985A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154214 | |||||||
| chr2:152154404 | A | T | 255 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(252): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.41-4175T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154404 | |||||||
| chr2:152154479 | G | A | 14 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0239 others(11): Show |
17 | HG00738.hp2 HG00741.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.41-4250C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154479 | |||||||
| chr2:152154601 | G | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0277 a0001c0001t0001g0278 others(1): Show |
6 | HG00558.hp2 HG00673.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-4372C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154601 | |||||||
| chr2:152154618 | T | TACAAA | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-4394_41-4390dup others(5): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154618 | |||||||
| chr2:152154700 | G | T | 1 | a0001c0001t0001g0267 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.41-4471C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154700 | |||||||
| chr2:152154800 | C | T | 3 | a0001c0001t0002g0058 a0001c0001t0002g0076 a0001c0001t0035g0077 |
3 | HG03017.hp1 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.41-4571G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154800 | |||||||
| chr2:152154961 | TG | T | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.41-4733delC | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154961 | |||||||
| chr2:152155120 | C | A | 10 | a0001c0001t0003g0018 a0001c0001t0003g0181 a0001c0001t0003g0223 others(7): Show |
11 | HG00609.hp1 HG03688.hp2 HG04184.hp2 others(8): Show |
intron_variant | MODIFIER | c.41-4891G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152155120 | |||||||
| chr2:152155193 | T | C | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.41-4964A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152155193 | |||||||
| chr2:152155616 | A | G | 210 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(207): Show |
233 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.41-5387T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152155616 | |||||||
| chr2:152155679 | G | A | 6 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(3): Show |
6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-5450C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152155679 | |||||||
| chr2:152156016 | C | T | 98 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(95): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-5787G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156016 | |||||||
| chr2:152156092 | T | A | 6 | a0001c0001t0001g0137 a0001c0001t0006g0135 a0001c0001t0006g0138 others(3): Show |
6 | HG01123.hp2 HG01167.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-5863A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156092 | |||||||
| chr2:152156438 | T | C | 1 | a0001c0001t0024g0225 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.41-6209A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156438 | |||||||
| chr2:152156446 | A | G | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-6217T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156446 | |||||||
| chr2:152156483 | G | A | 1 | a0001c0001t0006g0175 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.41-6254C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156483 | |||||||
| chr2:152156496 | G | C | 2 | a0001c0001t0001g0279 a0001c0001t0040g0280 |
2 | HG01106.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.41-6267C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156496 | |||||||
| chr2:152156539 | G | A | 1 | a0001c0001t0007g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.41-6310C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156539 | |||||||
| chr2:152156629 | A | G | 1 | a0001c0001t0004g0207 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.41-6400T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156629 | |||||||
| chr2:152156667 | T | A | 1 | a0001c0001t0005g0068 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.41-6438A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156667 | |||||||
| chr2:152156790 | C | A | 210 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(207): Show |
233 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.41-6561G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156790 | |||||||
| chr2:152156918 | G | A | 1 | a0001c0001t0009g0043 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.41-6689C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156918 | |||||||
| chr2:152157085 | A | C | 1 | a0001c0001t0003g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.41-6856T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152157085 | |||||||
| chr2:152157123 | T | A | 1 | a0001c0001t0002g0101 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.41-6894A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152157123 | |||||||
| chr2:152157649 | T | G | 1 | a0001c0001t0003g0249 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.41-7420A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152157649 | |||||||
| chr2:152157822 | A | C | 3 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 |
3 | HG02630.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.41-7593T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152157822 | |||||||
| chr2:152157889 | C | G | 1 | a0001c0001t0011g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.41-7660G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152157889 | |||||||
| chr2:152157927 | A | G | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.41-7698T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152157927 | |||||||
| chr2:152158170 | T | A | 1 | a0001c0001t0004g0213 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.41-7941A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158170 | |||||||
| chr2:152158202 | C | T | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-7973G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158202 | |||||||
| chr2:152158203 | G | A | 1 | a0001c0001t0008g0308 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.41-7974C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158203 | |||||||
| chr2:152158475 | C | CA | 11 | a0001c0001t0009g0038 a0001c0001t0009g0041 a0001c0001t0009g0042 others(8): Show |
11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.41-8247dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158475 | |||||||
| chr2:152158486 | T | A | 1 | a0001c0001t0007g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.41-8257A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158486 | |||||||
| chr2:152158596 | T | C | 1 | a0001c0001t0002g0126 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.41-8367A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158596 | |||||||
| chr2:152158690 | C | T | 1 | a0001c0001t0008g0305 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.41-8461G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158690 | |||||||
| chr2:152158773 | T | C | 1 | a0001c0001t0002g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.41-8544A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158773 | |||||||
| chr2:152158789 | T | C | 3 | a0001c0001t0017g0196 a0001c0001t0017g0202 a0001c0001t0017g0219 |
3 | HG00408.hp2 NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.41-8560A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158789 | |||||||
| chr2:152158836 | C | G | 3 | a0001c0001t0005g0066 a0001c0001t0005g0067 a0001c0001t0005g0068 |
3 | HG02015.hp2 HG02071.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.41-8607G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158836 | |||||||
| chr2:152159092 | A | C | 1 | a0001c0001t0008g0313 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.41-8863T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159092 | |||||||
| chr2:152159094 | C | CAT | 45 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(42): Show |
48 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.41-8867_41-8866dup others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATAT | 3 | a0001c0001t0003g0188 a0001c0001t0016g0105 a0001c0001t0016g0106 |
3 | HG03225.hp1 HG03942.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.41-8871_41-8866dup others(6): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATATA others(9): Show |
2 | a0001c0001t0004g0240 a0001c0001t0022g0241 |
2 | NA18968.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.41-8881_41-8866dup others(16): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATATA others(11): Show |
1 | a0001c0001t0014g0033 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.41-8866_41-8865ins others(18): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATATA others(15): Show |
1 | a0001c0001t0003g0221 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.41-8866_41-8865ins others(22): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATATA others(17): Show |
4 | a0001c0001t0003g0239 a0001c0001t0014g0031 a0001c0001t0014g0032 others(1): Show |
4 | HG01433.hp1 HG02109.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(24): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATATA others(19): Show |
5 | a0001c0001t0003g0178 a0001c0001t0003g0298 a0001c0001t0004g0215 others(2): Show |
5 | HG00738.hp2 HG02683.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(26): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATATA others(21): Show |
24 | a0001c0001t0003g0237 a0001c0001t0003g0245 a0001c0001t0003g0246 others(21): Show |
25 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(28): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATATA others(23): Show |
18 | a0001c0001t0003g0183 a0001c0001t0003g0234 a0001c0001t0003g0235 others(15): Show |
21 | HG01070.hp2 HG01361.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(30): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATATA others(25): Show |
9 | a0001c0001t0003g0182 a0001c0001t0003g0231 a0001c0001t0003g0247 others(6): Show |
9 | HG00408.hp2 HG00609.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(32): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATATA others(27): Show |
16 | a0001c0001t0003g0018 a0001c0001t0003g0228 a0001c0001t0003g0229 others(13): Show |
17 | HG00639.hp2 HG02015.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(34): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATATA others(29): Show |
13 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0218 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(36): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATATA others(31): Show |
7 | a0001c0001t0003g0179 a0001c0001t0003g0224 a0001c0001t0004g0195 others(4): Show |
7 | HG01243.hp1 HG02630.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(38): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATATA others(33): Show |
4 | a0001c0001t0003g0223 a0001c0001t0004g0193 a0001c0001t0023g0192 others(1): Show |
4 | HG01943.hp1 HG01981.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(40): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159094 | C | CATATATA others(47): Show |
1 | a0001c0001t0004g0191 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.41-8866_41-8865ins others(54): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | |||||||
| chr2:152159108 | T | TATATATA others(19): Show |
1 | a0001c0001t0003g0217 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.41-8880_41-8879ins others(26): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159108 | |||||||
| chr2:152159110 | T | TATATATA others(9): Show |
5 | a0001c0001t0002g0003 a0001c0001t0002g0086 a0001c0001t0002g0087 others(2): Show |
7 | HG02155.hp2 HG02165.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(16): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(11): Show |
1 | a0001c0001t0002g0088 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.41-8882_41-8881ins others(18): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(11): Show |
40 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(37): Show |
54 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(18): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(13): Show |
1 | a0001c0001t0002g0089 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.41-8882_41-8881ins others(20): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(13): Show |
14 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(11): Show |
14 | HG02015.hp2 HG02071.hp2 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(20): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(15): Show |
2 | a0001c0001t0008g0316 a0001c0001t0060g0312 |
2 | HG03688.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(22): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(15): Show |
14 | a0001c0001t0002g0062 a0001c0001t0005g0055 a0001c0001t0005g0065 others(11): Show |
15 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(22): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(17): Show |
6 | a0001c0001t0002g0093 a0001c0001t0005g0102 a0001c0001t0008g0309 others(3): Show |
6 | HG02027.hp2 HG02698.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(24): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(19): Show |
3 | a0001c0001t0003g0181 a0001c0001t0003g0242 a0001c0001t0024g0189 |
3 | HG04184.hp2 NA18943.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(26): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(21): Show |
2 | a0001c0001t0008g0317 a0001c0001t0009g0048 |
2 | HG03139.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(28): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(23): Show |
2 | a0001c0001t0009g0041 a0001c0001t0016g0029 |
2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(30): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(25): Show |
1 | a0001c0001t0009g0043 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.41-8882_41-8881ins others(32): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(27): Show |
3 | a0001c0001t0009g0042 a0001c0001t0009g0050 a0001c0001t0016g0028 |
3 | HG02145.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(34): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(35): Show |
1 | a0001c0001t0009g0045 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.41-8882_41-8881ins others(42): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(39): Show |
1 | a0001c0001t0009g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.41-8882_41-8881ins others(46): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(35): Show |
2 | a0001c0001t0009g0047 a0001c0001t0056g0049 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(42): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159110 | T | TATATATA others(39): Show |
1 | a0001c0001t0009g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.41-8882_41-8881ins others(46): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | |||||||
| chr2:152159207 | G | C | 1 | a0001c0001t0006g0299 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.41-8978C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159207 | |||||||
| chr2:152159325 | A | G | 1 | a0001c0001t0004g0222 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.41-9096T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159325 | |||||||
| chr2:152159538 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.41-9309G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159538 | |||||||
| chr2:152159577 | T | G | 3 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 |
3 | HG02630.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.41-9348A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159577 | |||||||
| chr2:152159585 | G | A | 98 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(95): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-9356C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159585 | |||||||
| chr2:152159735 | A | G | 1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.41-9506T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159735 | |||||||
| chr2:152159874 | G | A | 1 | a0001c0001t0024g0189 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.41-9645C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159874 | |||||||
| chr2:152159876 | G | A | 98 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(95): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-9647C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159876 | |||||||
| chr2:152159896 | T | C | 98 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(95): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-9667A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159896 | |||||||
| chr2:152159920 | G | C | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.41-9691C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159920 | |||||||
| chr2:152159940 | G | A | 3 | a0001c0001t0003g0178 a0001c0001t0003g0252 a0001c0001t0022g0243 |
3 | HG02683.hp2 HG02738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.41-9711C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159940 | |||||||
| chr2:152159973 | T | C | 1 | a0001c0001t0039g0281 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.41-9744A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159973 | |||||||
| chr2:152159978 | G | C | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-9749C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159978 | |||||||
| chr2:152159999 | A | G | 210 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(207): Show |
233 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.41-9770T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159999 | |||||||
| chr2:152160062 | G | A | 98 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(95): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-9833C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160062 | |||||||
| chr2:152160070 | G | A | 4 | a0001c0001t0009g0046 a0001c0001t0009g0047 a0001c0001t0009g0048 others(1): Show |
4 | HG02145.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-9841C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160070 | |||||||
| chr2:152160098 | G | A | 1 | a0001c0001t0002g0089 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.41-9869C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160098 | |||||||
| chr2:152160149 | A | AC | 6 | a0001c0001t0002g0062 a0001c0001t0003g0221 a0001c0001t0008g0308 others(3): Show |
6 | HG00621.hp2 HG01261.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-9921dupG | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160149 | |||||||
| chr2:152160157 | G | A | 1 | a0001c0001t0046g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.41-9928C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160157 | |||||||
| chr2:152160257 | C | T | 62 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(59): Show |
78 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.41-10028G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160257 | |||||||
| chr2:152160297 | C | T | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-10068G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160297 | |||||||
| chr2:152160325 | A | G | 1 | a0001c0001t0057g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.41-10096T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160325 | |||||||
| chr2:152160342 | G | A | 1 | a0001c0001t0003g0218 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.41-10113C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160342 | |||||||
| chr2:152160386 | G | A | 1 | a0001c0001t0044g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.41-10157C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160386 | |||||||
| chr2:152160404 | G | A | 1 | a0001c0001t0017g0219 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.41-10175C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160404 | |||||||
| chr2:152160547 | G | A | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-10318C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160547 | |||||||
| chr2:152160614 | C | T | 1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.41-10385G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160614 | |||||||
| chr2:152160648 | G | A | 64 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(61): Show |
80 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.41-10419C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160648 | |||||||
| chr2:152160652 | G | A | 2 | a0001c0001t0005g0090 a0001c0001t0005g0091 |
2 | NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.41-10423C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160652 | |||||||
| chr2:152160655 | G | T | 1 | a0001c0001t0001g0266 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.41-10426C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160655 | |||||||
| chr2:152160670 | G | A | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.41-10441C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160670 | |||||||
| chr2:152160682 | C | T | 1 | a0001c0001t0006g0299 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.41-10453G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160682 | |||||||
| chr2:152160683 | G | A | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-10454C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160683 | |||||||
| chr2:152160686 | C | T | 88 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-10457G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160686 | |||||||
| chr2:152160687 | G | A | 1 | a0001c0001t0059g0314 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.41-10458C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160687 | |||||||
| chr2:152160710 | C | G | 2 | a0001c0001t0007g0115 a0001c0001t0055g0116 |
2 | HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.41-10481G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160710 | |||||||
| chr2:152160726 | T | C | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.41-10497A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160726 | |||||||
| chr2:152160736 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.41-10507C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160736 | |||||||
| chr2:152160749 | T | C | 257 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0264 others(254): Show |
283 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.41-10520A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160749 | |||||||
| chr2:152160759 | C | T | 4 | a0001c0002t0018g0151 a0001c0002t0018g0153 a0001c0002t0018g0154 others(1): Show |
4 | HG02559.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-10530G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160759 | |||||||
| chr2:152160760 | G | A | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.41-10531C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160760 | |||||||
| chr2:152160772 | C | T | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.41-10543G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160772 | |||||||
| chr2:152160772 | CGGGAAGT others(169): Show |
C | 1 | a0001c0001t0004g0251 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.41-10719_41-10544d others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160772 | |||||||
| chr2:152160799 | C | A | 98 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(95): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-10570G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160799 | |||||||
| chr2:152160841 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.41-10612G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160841 | |||||||
| chr2:152160846 | G | A | 87 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(84): Show |
93 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.41-10617C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160846 | |||||||
| chr2:152160904 | C | A | 1 | a0001c0001t0002g0094 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.41-10675G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160904 | |||||||
| chr2:152160908 | A | ATCCGGGA others(169): Show |
2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.41-10680_41-10679i others(178): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160908 | |||||||
| chr2:152160908 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.41-10679T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160908 | |||||||
| chr2:152160936 | A | G | 88 | a0001c0001t0002g0061 a0001c0001t0003g0018 a0001c0001t0003g0178 others(85): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-10707T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160936 | |||||||
| chr2:152161031 | C | T | 2 | a0001c0001t0003g0188 a0001c0001t0003g0247 |
2 | HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.41-10802G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161031 | |||||||
| chr2:152161056 | G | C | 9 | a0001c0001t0003g0188 a0001c0001t0003g0247 a0001c0001t0011g0140 others(6): Show |
9 | HG01192.hp2 HG02280.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-10827C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161056 | |||||||
| chr2:152161059 | G | C | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-10830C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161059 | |||||||
| chr2:152161087 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | NA18981.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.41-10858G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161087 | |||||||
| chr2:152161099 | G | A | 1 | a0001c0001t0015g0283 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.41-10870C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161099 | |||||||
| chr2:152161260 | G | A | 255 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(252): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.41-11031C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161260 | |||||||
| chr2:152161278 | T | C | 80 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(77): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.41-11049A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161278 | |||||||
| chr2:152161307 | G | C | 80 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(77): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.41-11078C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161307 | |||||||
| chr2:152161440 | T | C | 1 | a0001c0001t0045g0244 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.41-11211A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161440 | |||||||
| chr2:152161494 | TA | T | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.41-11266delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161494 | |||||||
| chr2:152161494 | TAA | T | 32 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0012g0159 others(29): Show |
32 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.41-11267_41-11266d others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161494 | |||||||
| chr2:152161507 | A | C | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-11278T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161507 | |||||||
| chr2:152161512 | A | C | 2 | a0001c0001t0002g0097 a0001c0001t0032g0103 |
2 | HG00280.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.41-11283T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161512 | |||||||
| chr2:152161689 | A | G | 1 | a0001c0001t0019g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.41-11460T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161689 | |||||||
| chr2:152162450 | C | T | 1 | a0001c0001t0024g0189 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.41-12221G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162450 | |||||||
| chr2:152162506 | G | A | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(53): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.41-12277C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162506 | |||||||
| chr2:152162786 | G | A | 2 | a0001c0001t0042g0161 a0001c0001t0046g0176 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.41-12557C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162786 | |||||||
| chr2:152162789 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.41-12560G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162789 | |||||||
| chr2:152162807 | A | AT | 233 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(230): Show |
258 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.41-12579dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162807 | |||||||
| chr2:152162807 | A | ATT | 12 | a0001c0001t0005g0055 a0001c0001t0008g0027 a0001c0001t0008g0313 others(9): Show |
13 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.41-12580_41-12579d others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162807 | |||||||
| chr2:152162810 | T | TC | 6 | a0001c0001t0012g0163 a0001c0001t0012g0164 a0001c0001t0012g0165 others(3): Show |
6 | HG00639.hp1 HG02572.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-12582_41-12581i others(3): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162810 | |||||||
| chr2:152162913 | G | C | 6 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(3): Show |
6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-12684C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162913 | |||||||
| chr2:152162921 | A | T | 11 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(8): Show |
11 | HG00639.hp1 HG01070.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.40+12682T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162921 | |||||||
| chr2:152162953 | C | T | 12 | a0001c0001t0007g0010 a0001c0001t0007g0040 a0001c0001t0007g0115 others(9): Show |
14 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.40+12650G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162953 | |||||||
| chr2:152162983 | A | C | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.40+12620T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162983 | |||||||
| chr2:152163061 | A | G | 1 | a0001c0001t0003g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.40+12542T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163061 | |||||||
| chr2:152163200 | G | A | 1 | a0001c0001t0053g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.40+12403C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163200 | |||||||
| chr2:152163251 | A | C | 2 | a0001c0001t0008g0306 a0001c0001t0008g0307 |
2 | HG01081.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.40+12352T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163251 | |||||||
| chr2:152163350 | C | G | 11 | a0001c0001t0008g0027 a0001c0001t0008g0313 a0001c0001t0008g0315 others(8): Show |
12 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.40+12253G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163350 | |||||||
| chr2:152163399 | C | T | 1 | a0001c0001t0046g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+12204G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163399 | |||||||
| chr2:152163610 | G | T | 93 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(90): Show |
100 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.40+11993C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163610 | |||||||
| chr2:152163732 | A | C | 24 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(21): Show |
25 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.40+11871T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163732 | |||||||
| chr2:152163743 | C | G | 1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.40+11860G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163743 | |||||||
| chr2:152164031 | T | C | 3 | a0001c0001t0020g0170 a0001c0001t0021g0171 a0001c0001t0021g0172 |
3 | HG02257.hp2 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.40+11572A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164031 | |||||||
| chr2:152164098 | A | G | 255 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(252): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.40+11505T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164098 | |||||||
| chr2:152164125 | G | A | 1 | a0001c0001t0046g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+11478C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164125 | |||||||
| chr2:152164139 | T | C | 1 | a0001c0001t0038g0092 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.40+11464A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164139 | |||||||
| chr2:152164219 | A | G | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | HG00609.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.40+11384T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164219 | |||||||
| chr2:152164570 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.40+11033C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164570 | |||||||
| chr2:152164693 | C | T | 93 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(90): Show |
109 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.40+10910G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164693 | |||||||
| chr2:152164753 | A | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.40+10850T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164753 | |||||||
| chr2:152164795 | T | C | 1 | a0001c0001t0041g0286 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.40+10808A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164795 | |||||||
| chr2:152164804 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0015g0111 a0001c0001t0015g0112 |
3 | HG02055.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.40+10799G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164804 | |||||||
| chr2:152164912 | T | C | 1 | a0001c0001t0003g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.40+10691A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164912 | |||||||
| chr2:152164917 | C | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.40+10686G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164917 | |||||||
| chr2:152165024 | C | A | 2 | a0001c0001t0006g0147 a0001c0001t0006g0148 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.40+10579G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165024 | |||||||
| chr2:152165056 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.40+10547G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165056 | |||||||
| chr2:152165075 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.40+10528A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165075 | |||||||
| chr2:152165169 | C | T | 82 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(79): Show |
88 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.40+10434G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165169 | |||||||
| chr2:152165261 | T | TA | 7 | a0001c0001t0001g0289 a0001c0001t0014g0031 a0001c0001t0014g0032 others(4): Show |
7 | HG01167.hp2 HG01358.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+10341dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165261 | |||||||
| chr2:152165355 | C | A | 3 | a0001c0001t0001g0113 a0001c0001t0015g0111 a0001c0001t0015g0112 |
3 | HG02055.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.40+10248G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165355 | |||||||
| chr2:152165469 | A | G | 82 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(79): Show |
88 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.40+10134T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165469 | |||||||
| chr2:152165557 | C | T | 82 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(79): Show |
88 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.40+10046G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165557 | |||||||
| chr2:152165842 | T | C | 3 | a0001c0001t0007g0120 a0001c0001t0007g0121 a0001c0001t0007g0122 |
3 | HG02109.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.40+9761A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165842 | |||||||
| chr2:152165869 | C | T | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.40+9734G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165869 | |||||||
| chr2:152165924 | C | T | 1 | a0001c0001t0057g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.40+9679G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165924 | |||||||
| chr2:152165959 | G | T | 81 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(78): Show |
87 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.40+9644C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165959 | |||||||
| chr2:152165977 | C | T | 1 | a0001c0001t0008g0305 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.40+9626G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165977 | |||||||
| chr2:152166005 | C | T | 1 | a0001c0001t0009g0041 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.40+9598G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166005 | |||||||
| chr2:152166065 | T | C | 2 | a0001c0001t0051g0095 a0001c0001t0052g0096 |
2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.40+9538A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166065 | |||||||
| chr2:152166085 | C | A | 1 | a0001c0001t0043g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.40+9518G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166085 | |||||||
| chr2:152166091 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.40+9512A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166091 | |||||||
| chr2:152166166 | T | A | 3 | a0001c0001t0020g0155 a0001c0001t0020g0156 a0001c0001t0043g0157 |
3 | HG02258.hp1 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.40+9437A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166166 | |||||||
| chr2:152166176 | AAAC | A | 80 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(77): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.40+9424_40+9426del others(3): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166176 | |||||||
| chr2:152166375 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.40+9228C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166375 | |||||||
| chr2:152166492 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.40+9111G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166492 | |||||||
| chr2:152166646 | G | C | 254 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(251): Show |
280 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.40+8957C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166646 | |||||||
| chr2:152166829 | C | A | 1 | a0001c0001t0008g0316 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.40+8774G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166829 | |||||||
| chr2:152167085 | TTCA | T | 5 | a0001c0001t0016g0028 a0001c0001t0016g0029 a0001c0001t0016g0104 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+8515_40+8517del others(3): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167085 | |||||||
| chr2:152167111 | T | A | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.40+8492A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167111 | |||||||
| chr2:152167236 | T | G | 82 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(79): Show |
88 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.40+8367A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167236 | |||||||
| chr2:152167459 | G | T | 1 | a0001c0001t0002g0052 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.40+8144C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167459 | |||||||
| chr2:152167508 | T | C | 1 | a0001c0001t0003g0247 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.40+8095A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167508 | |||||||
| chr2:152167599 | G | A | 255 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(252): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.40+8004C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167599 | |||||||
| chr2:152167670 | G | C | 5 | a0001c0001t0016g0028 a0001c0001t0016g0029 a0001c0001t0016g0104 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+7933C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167670 | |||||||
| chr2:152167731 | G | GA | 171 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(168): Show |
191 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.40+7871dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167731 | |||||||
| chr2:152167735 | A | AT | 83 | a0001c0001t0002g0051 a0001c0001t0003g0018 a0001c0001t0003g0178 others(80): Show |
89 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.40+7867_40+7868ins others(1): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167735 | |||||||
| chr2:152167739 | T | A | 8 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(5): Show |
8 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.40+7864A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167739 | |||||||
| chr2:152167921 | A | AAAAAT | 3 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0001c0001t0004g0186 |
3 | HG02630.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.40+7677_40+7681dup others(5): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167921 | |||||||
| chr2:152168163 | AT | A | 82 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(79): Show |
88 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.40+7439delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168163 | |||||||
| chr2:152168171 | T | G | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.40+7432A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168171 | |||||||
| chr2:152168286 | G | A | 11 | a0001c0001t0009g0038 a0001c0001t0009g0041 a0001c0001t0009g0042 others(8): Show |
11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.40+7317C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168286 | |||||||
| chr2:152168401 | G | A | 1 | a0001c0001t0003g0247 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.40+7202C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168401 | |||||||
| chr2:152168448 | G | A | 1 | a0001c0001t0013g0025 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.40+7155C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168448 | |||||||
| chr2:152168449 | C | T | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.40+7154G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168449 | |||||||
| chr2:152168516 | G | C | 80 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(77): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.40+7087C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168516 | |||||||
| chr2:152168591 | C | T | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.40+7012G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168591 | |||||||
| chr2:152168829 | C | T | 7 | a0001c0001t0020g0155 a0001c0001t0020g0156 a0001c0001t0043g0157 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.40+6774G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168829 | |||||||
| chr2:152168905 | C | A | 1 | a0001c0001t0056g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.40+6698G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168905 | |||||||
| chr2:152168973 | T | A | 2 | a0001c0001t0013g0290 a0001c0001t0013g0295 |
2 | HG01074.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.40+6630A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168973 | |||||||
| chr2:152169064 | T | C | 82 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(79): Show |
88 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.40+6539A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169064 | |||||||
| chr2:152169151 | G | C | 312 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(309): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.40+6452C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169151 | |||||||
| chr2:152169246 | T | C | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.40+6357A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169246 | |||||||
| chr2:152169275 | C | A | 1 | a0001c0001t0013g0291 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.40+6328G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169275 | |||||||
| chr2:152169423 | C | A | 1 | a0001c0001t0009g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.40+6180G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169423 | |||||||
| chr2:152169593 | A | C | 1 | a0001c0002t0018g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.40+6010T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169593 | |||||||
| chr2:152169856 | C | CT | 61 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(58): Show |
77 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.40+5746dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169856 | |||||||
| chr2:152169856 | CT | C | 9 | a0001c0001t0001g0292 a0001c0001t0006g0303 a0001c0001t0007g0114 others(6): Show |
9 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.40+5746delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169856 | |||||||
| chr2:152169910 | G | A | 1 | a0001c0001t0011g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.40+5693C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169910 | |||||||
| chr2:152170028 | C | G | 312 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(309): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.40+5575G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170028 | |||||||
| chr2:152170115 | G | A | 1 | a0001c0001t0008g0317 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.40+5488C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170115 | |||||||
| chr2:152170356 | G | A | 1 | a0001c0001t0007g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.40+5247C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170356 | |||||||
| chr2:152170444 | C | T | 82 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(79): Show |
88 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.40+5159G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170444 | |||||||
| chr2:152170482 | CA | C | 185 | a0001c0001t0001g0258 a0001c0001t0002g0001 a0001c0001t0002g0003 others(182): Show |
208 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.40+5120delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170482 | |||||||
| chr2:152170601 | G | A | 1 | a0001c0001t0003g0249 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.40+5002C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170601 | |||||||
| chr2:152170680 | A | C | 1 | a0001c0001t0054g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.40+4923T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170680 | |||||||
| chr2:152170799 | T | C | 1 | a0001c0001t0032g0103 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.40+4804A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170799 | |||||||
| chr2:152170937 | A | G | 1 | a0001c0001t0003g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.40+4666T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170937 | |||||||
| chr2:152171090 | T | C | 1 | a0001c0001t0020g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.40+4513A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171090 | |||||||
| chr2:152171114 | T | C | 2 | a0001c0001t0006g0147 a0001c0001t0006g0148 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.40+4489A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171114 | |||||||
| chr2:152171151 | C | T | 1 | a0001c0002t0018g0151 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.40+4452G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171151 | |||||||
| chr2:152171260 | T | G | 1 | a0001c0001t0007g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40+4343A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171260 | |||||||
| chr2:152171425 | C | CTT | 255 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0001 others(252): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.40+4176_40+4177dup others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171425 | |||||||
| chr2:152171633 | T | C | 1 | a0001c0001t0044g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.40+3970A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171633 | |||||||
| chr2:152171891 | G | C | 1 | a0001c0001t0007g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.40+3712C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171891 | |||||||
| chr2:152171960 | G | T | 11 | a0001c0001t0009g0038 a0001c0001t0009g0041 a0001c0001t0009g0042 others(8): Show |
11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.40+3643C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171960 | |||||||
| chr2:152172553 | G | A | 82 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(79): Show |
88 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.40+3050C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172553 | |||||||
| chr2:152172577 | G | T | 7 | a0001c0001t0001g0258 a0001c0001t0014g0031 a0001c0001t0014g0032 others(4): Show |
7 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+3026C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172577 | |||||||
| chr2:152172578 | G | C | 1 | a0001c0001t0001g0256 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.40+3025C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172578 | |||||||
| chr2:152172611 | G | A | 12 | a0001c0001t0007g0010 a0001c0001t0007g0040 a0001c0001t0007g0115 others(9): Show |
14 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.40+2992C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172611 | |||||||
| chr2:152172632 | G | A | 5 | a0001c0001t0016g0028 a0001c0001t0016g0029 a0001c0001t0016g0104 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+2971C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172632 | |||||||
| chr2:152172682 | A | G | 1 | a0001c0001t0046g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+2921T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172682 | |||||||
| chr2:152172747 | T | C | 1 | a0001c0001t0002g0126 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.40+2856A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172747 | |||||||
| chr2:152172796 | G | A | 98 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0013 others(95): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.40+2807C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172796 | |||||||
| chr2:152172862 | C | CA | 6 | a0001c0001t0016g0028 a0001c0001t0016g0029 a0001c0001t0016g0104 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+2740dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172862 | |||||||
| chr2:152172862 | CA | C | 6 | a0001c0001t0001g0257 a0001c0001t0001g0293 a0001c0001t0003g0182 others(3): Show |
6 | HG01168.hp2 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+2740delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172862 | |||||||
| chr2:152172874 | A | G | 1 | a0001c0001t0003g0181 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.40+2729T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172874 | |||||||
| chr2:152173207 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.40+2396C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173207 | |||||||
| chr2:152173210 | C | CA | 6 | a0001c0001t0001g0294 a0001c0001t0002g0126 a0001c0001t0003g0250 others(3): Show |
6 | HG01074.hp1 HG01074.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+2392dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173210 | |||||||
| chr2:152173355 | T | C | 2 | a0001c0001t0006g0149 a0001c0001t0006g0150 |
2 | NA18957.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.40+2248A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173355 | |||||||
| chr2:152173361 | C | CACATATA others(23): Show |
2 | a0001c0001t0003g0179 a0001c0001t0046g0176 |
2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.40+2212_40+2241dup others(30): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173361 | |||||||
| chr2:152173361 | C | CACATATA others(51): Show |
1 | a0001c0001t0044g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.40+2241_40+2242ins others(58): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173361 | |||||||
| chr2:152173361 | C | CACATATA others(21): Show |
76 | a0001c0001t0003g0018 a0001c0001t0003g0181 a0001c0001t0003g0182 others(73): Show |
82 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.40+2241_40+2242ins others(28): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173361 | |||||||
| chr2:152173361 | C | CACATATA others(51): Show |
1 | a0001c0001t0003g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.40+2241_40+2242ins others(58): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173361 | |||||||
| chr2:152173365 | T | C | 31 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0006g0026 others(28): Show |
32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.40+2238A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173365 | |||||||
| chr2:152173375 | T | TATATATA others(19): Show |
1 | a0001c0001t0003g0252 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.40+2227_40+2228ins others(26): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173375 | |||||||
| chr2:152173395 | T | C | 24 | a0001c0001t0012g0159 a0001c0001t0012g0160 a0001c0001t0012g0163 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.40+2208A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173395 | |||||||
| chr2:152173404 | A | AT | 6 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(3): Show |
6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+2198dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173404 | |||||||
| chr2:152173406 | A | ACGTATAT others(93): Show |
1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.40+2196_40+2197ins others(100): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173406 | |||||||
| chr2:152173406 | A | T | 186 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(183): Show |
208 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.40+2197T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173406 | |||||||
| chr2:152173408 | T | A | 1 | a0001c0004t0018g0174 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.40+2195A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173408 | |||||||
| chr2:152173543 | C | T | 1 | a0001c0001t0009g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.40+2060G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173543 | |||||||
| chr2:152173555 | C | T | 1 | a0001c0001t0013g0253 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.40+2048G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173555 | |||||||
| chr2:152173751 | T | C | 1 | a0001c0001t0006g0175 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.40+1852A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173751 | |||||||
| chr2:152173776 | C | G | 1 | a0001c0001t0046g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+1827G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173776 | |||||||
| chr2:152174076 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.40+1527C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174076 | |||||||
| chr2:152174243 | C | T | 1 | a0001c0001t0046g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+1360G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174243 | |||||||
| chr2:152174355 | G | A | 82 | a0001c0001t0003g0018 a0001c0001t0003g0178 a0001c0001t0003g0179 others(79): Show |
88 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.40+1248C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174355 | |||||||
| chr2:152174599 | T | C | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(53): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.40+1004A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174599 | |||||||
| chr2:152174879 | T | C | 2 | a0001c0001t0007g0010 a0001c0001t0007g0297 |
4 | HG02922.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+724A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174879 | |||||||
| chr2:152174920 | G | C | 1 | a0001c0001t0003g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.40+683C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174920 | |||||||
| chr2:152174957 | T | C | 6 | a0001c0001t0006g0026 a0001c0001t0006g0299 a0001c0001t0006g0300 others(3): Show |
7 | HG01081.hp2 HG01358.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.40+646A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174957 | |||||||
| chr2:152175488 | C | T | 2 | a0001c0001t0016g0028 a0001c0001t0016g0029 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.40+115G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152175488 |